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Search for "inclusion body myopathy" English only.

1: Forman MS, Mackenzie IR, Cairns NJ, Swanson E, Boyer PJ, Drachman DA,
Jhaveri BS, Karlawish JH, Pestronk A, Smith TW, Tu PH, Watts GD, Markesbery WR,
Smith CD, Kimonis VE.
Novel Ubiquitin Neuropathology in Frontotemporal Dementia With
Valosin-Containing Protein Gene Mutations.
J Neuropathol Exp Neurol. 2006 Jun;65(6):571-581.
PMID: 16783167 [PubMed - as supplied by publisher]

2: Savelkoul PJ, Manoli I, Sparks SE, Ciccone C, Gahl WA, Krasnewich DM,
Huizing M.
Normal sialylation of serum N-linked and O-GalNAc-linked glycans in hereditary
inclusion-body myopathy.
Mol Genet Metab. 2006 Jun 6; [Epub ahead of print] No abstract available.
PMID: 16762577 [PubMed - as supplied by publisher]

3: Fischer D, Clemen CS, Olive M, Ferrer I, Goudeau B, Roth U, Badorf P,
Wattjes MP, Lutterbey G, Kral T, van der Ven PF, Furst DO, Vicart P, Goldfarb
LG, Moza M, Carpen O, Reichelt J, Schroder R.
Different early pathogenesis in myotilinopathy compared to primary
desminopathy.
Neuromuscul Disord. 2006 Jun;16(6):361-7. Epub 2006 May 8.
PMID: 16684602 [PubMed - in process]

4: Pavlu J, Carey MP, Winer JB.
Hypothyroidism and nemaline myopathy in an adult.
J Neurol Neurosurg Psychiatry. 2006 May;77(5):708-9. No abstract available.
PMID: 16614046 [PubMed - indexed for MEDLINE]

5: Uyama E, Hino H, Araki K, Takeya M, Uchino M, Yamamura K.
Animal model of oculopharyngeal muscular dystrophy.
Acta Myol. 2005 Oct;24(2):84-8.
PMID: 16550922 [PubMed - indexed for MEDLINE]

6: Nishino I, Malicdan MC, Murayama K, Nonaka I, Hayashi YK, Noguchi S.
Molecular pathomechanism of distal myopathy with rimmed vacuoles.
Acta Myol. 2005 Oct;24(2):80-3. Review.
PMID: 16550921 [PubMed - indexed for MEDLINE]

7: Ricci E, Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, Frusciante R, Di
Lella GM, Tonali PA, Mirabella M.
NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE
mutations.
Neurology. 2006 Mar 14;66(5):755-8.
PMID: 16534119 [PubMed - indexed for MEDLINE]

8: Penner J, Mantey LR, Elgavish S, Ghaderi D, Cirak S, Berger M, Krause S,
Lucka L, Voit T, Mitrani-Rosenbaum S, Hinderlich S.
Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary
inclusion body myopathy.
Biochemistry. 2006 Mar 7;45(9):2968-77.
PMID: 16503651 [PubMed - indexed for MEDLINE]

9: Toriumi Y, Takusa Y, Uchiyama A, Kimura M, Sejima H, Yamaguchi S, Eda I,
Nishino I, Nonaka I.
Distal myopathy with rimmed vacuoles in a case of opercular syndrome.
Brain Dev. 2006 Feb 24; [Epub ahead of print]
PMID: 16503389 [PubMed - as supplied by publisher]

10: Dimitri D, Benveniste O, Dubourg O, Maisonobe T, Eymard B, Amoura Z, Jean
L, Tiev K, Piette JC, Klatzmann D, Herson S, Boyer O.
Shared blood and muscle CD8+ T-cell expansions in inclusion body myositis.
Brain. 2006 Apr;129(Pt 4):986-95. Epub 2006 Feb 2.
PMID: 16455793 [PubMed - indexed for MEDLINE]

11: Nogalska A, Engel WK, McFerrin J, Kokame K, Komano H, Askanas V.
Homocysteine-induced endoplasmic reticulum protein (Herp) is up-regulated in
sporadic inclusion-body myositis and in endoplasmic reticulum stress-induced
cultured human muscle fibers.
J Neurochem. 2006 Mar;96(5):1491-9. Epub 2006 Jan 25.
PMID: 16441512 [PubMed - indexed for MEDLINE]

12: Moreira PI, Honda K, Zhu X, Nunomura A, Casadesus G, Smith MA, Perry G.
Brain and brawn: parallels in oxidative strength.
Neurology. 2006 Jan 24;66(2 Suppl 1):S97-101. Review.
PMID: 16432155 [PubMed - indexed for MEDLINE]

13: Davies KJ, Shringarpure R.
Preferential degradation of oxidized proteins by the 20S proteasome may be
inhibited in aging and in inflammatory neuromuscular diseases.
Neurology. 2006 Jan 24;66(2 Suppl 1):S93-6. Review.
PMID: 16432154 [PubMed - indexed for MEDLINE]

14: Glabe CG, Kayed R.
Common structure and toxic function of amyloid oligomers implies a common
mechanism of pathogenesis.
Neurology. 2006 Jan 24;66(2 Suppl 1):S74-8. Review.
PMID: 16432151 [PubMed - indexed for MEDLINE]

15: Murphy MP, Golde TE.
Inclusion-body myositis and Alzheimer disease: two sides of the same coin, or
different currencies altogether?
Neurology. 2006 Jan 24;66(2 Suppl 1):S65-8. Review. No abstract available.
PMID: 16432148 [PubMed - indexed for MEDLINE]

16: McGavern DB.
Immunotherapeutic relief from persistent infections and amyloid disorders.
Neurology. 2006 Jan 24;66(2 Suppl 1):S59-64. Review.
PMID: 16432147 [PubMed - indexed for MEDLINE]

17: Steinman L.
Controlling autoimmunity in sporadic inclusion-body myositis.
Neurology. 2006 Jan 24;66(2 Suppl 1):S56-8. Review. No abstract available.
PMID: 16432146 [PubMed - indexed for MEDLINE]

18: Oldfors A, Moslemi AR, Jonasson L, Ohlsson M, Kollberg G, Lindberg C.
Mitochondrial abnormalities in inclusion-body myositis.
Neurology. 2006 Jan 24;66(2 Suppl 1):S49-55. Review.
PMID: 16432145 [PubMed - indexed for MEDLINE]

19: Askanas V, Engel WK.
Inclusion-body myositis: a myodegenerative conformational disorder associated
with Abeta, protein misfolding, and proteasome inhibition.
Neurology. 2006 Jan 24;66(2 Suppl 1):S39-48. Review.
PMID: 16432144 [PubMed - indexed for MEDLINE]

20: Dalakas MC.
Inflammatory, immune, and viral aspects of inclusion-body myositis.
Neurology. 2006 Jan 24;66(2 Suppl 1):S33-8. Review.
PMID: 16432143 [PubMed - indexed for MEDLINE]

21: Griggs RC.
The current status of treatment for inclusion-body myositis.
Neurology. 2006 Jan 24;66(2 Suppl 1):S30-2. Review.
PMID: 16432142 [PubMed - indexed for MEDLINE]

22: Engel WK, Askanas V.
Inclusion-body myositis: clinical, diagnostic, and pathologic aspects.
Neurology. 2006 Jan 24;66(2 Suppl 1):S20-9. Review.
PMID: 16432141 [PubMed - indexed for MEDLINE]

23: Barohn RJ, Herbelin L, Kissel JT, King W, McVey AL, Saperstein DS, Mendell
JR.
Pilot trial of etanercept in the treatment of inclusion-body myositis.
Neurology. 2006 Jan 24;66(2 Suppl 1):S123-4.
PMID: 16432140 [PubMed - indexed for MEDLINE]

24: Paulson H.
RNA interference as potential therapy for neurodegenerative disease:
applications to inclusion-body myositis?
Neurology. 2006 Jan 24;66(2 Suppl 1):S114-7. Review.
PMID: 16432138 [PubMed - indexed for MEDLINE]

25: Buxbaum JN.
Treatment and prevention of the amyloidoses: can the lessons learned be applied
to sporadic inclusion-body myositis?
Neurology. 2006 Jan 24;66(2 Suppl 1):S110-3. Review.
PMID: 16432137 [PubMed - indexed for MEDLINE]

26: Finch CE.
A perspective on sporadic inclusion-body myositis: the role of aging and
inflammatory processes.
Neurology. 2006 Jan 24;66(2 Suppl 1):S1-6. Review.
PMID: 16432135 [PubMed - indexed for MEDLINE]

27: Sallum AM, Kiss MH, Silva CA, Wakamatsu A, Vianna MA, Sachetti S, Marie SK.

Difference in adhesion molecule expression (ICAM-1 and VCAM-1) in juvenile and
adult dermatomyositis, polymyositis and inclusion body myositis.
Autoimmun Rev. 2006 Feb;5(2):93-100. Epub 2005 Jun 17. Review.
PMID: 16431335 [PubMed - indexed for MEDLINE]

28: Reddy SV.
Etiologic factors in Paget's disease of bone.
Cell Mol Life Sci. 2006 Feb;63(4):391-8.
PMID: 16429324 [PubMed - indexed for MEDLINE]

29: Hutchinson DO, Charlton A, Laing NG, Ilkovski B, North KN.
Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of
the skeletal muscle ACTA1 gene: clinical and pathological variability within a
kindred.
Neuromuscul Disord. 2006 Feb;16(2):113-21. Epub 2006 Jan 19.
PMID: 16427282 [PubMed - indexed for MEDLINE]

30: Hengstman GJ, Vree Egberts WT, Seelig HP, Lundberg IE, Moutsopoulos HM,
Doria A, Mosca M, Vencovsky J, van Venrooij WJ, van Engelen BG.
Clinical characteristics of patients with myositis and autoantibodies to
different fragments of the Mi-2 beta antigen.
Ann Rheum Dis. 2006 Feb;65(2):242-5.
PMID: 16410528 [PubMed - indexed for MEDLINE]

31: Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, Servidei T, Pescatori M,
Tonali PA, Ricci E, Mirabella M.
Neprilysin participates in skeletal muscle regeneration and is accumulated in
abnormal muscle fibres of inclusion body myositis.
J Neurochem. 2006 Feb;96(3):777-89. Epub 2006 Jan 9.
PMID: 16405511 [PubMed - indexed for MEDLINE]

32: Dalakas MC.
Intravenous immunoglobulin in patients with anti-GAD antibody-associated
neurological diseases and patients with inflammatory myopathies: effects on
clinicopathological features and immunoregulatory genes.
Clin Rev Allergy Immunol. 2005 Dec;29(3):255-69.
PMID: 16391401 [PubMed - indexed for MEDLINE]

33: Rodolico C, Toscano A, Patitucci A, Muglia M, Gaeta M, D'Arrigo G,
Migliorato A, Messina S, Quattrone A, Messina C, Vita G.
Clinical and muscle magnetic resonance imaging study of an Italian family with
autosomal dominant inclusion body myopathy not linked to known genetic loci.
Neurol Sci. 2005 Dec;26(5):303-9.
PMID: 16388363 [PubMed - indexed for MEDLINE]

34: Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L,
Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC.
A mutation in myotilin causes spheroid body myopathy.
Neurology. 2005 Dec 27;65(12):1936-40.
PMID: 16380616 [PubMed - indexed for MEDLINE]

35: Munshi SK, Thanvi B, Jonnalagadda SJ, Da Forno P, Patel A, Sharma S.
Inclusion body myositis: an underdiagnosed myopathy of older people.
Age Ageing. 2006 Jan;35(1):91-4.
PMID: 16364943 [PubMed - indexed for MEDLINE]

36: Chiappetta N, Steier J, Gruber B.
Rituximab in the treatment of refractory dermatomyositis.
J Clin Rheumatol. 2005 Oct;11(5):264-6.
PMID: 16357773 [PubMed - indexed for MEDLINE]

37: Greenberg SA, Bradshaw EM, Pinkus JL, Pinkus GS, Burleson T, Due B, Bregoli
L, O'Connor KC, Amato AA.
Plasma cells in muscle in inclusion body myositis and polymyositis.
Neurology. 2005 Dec 13;65(11):1782-7. Erratum in: Neurology. 2006 Feb
28;66(4):493. Bregoli, L S [corrected to Bregoli, L].
PMID: 16344523 [PubMed - indexed for MEDLINE]

38: Weihl CC, Dalal S, Pestronk A, Hanson PI.
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic
reticulum-associated degradation.
Hum Mol Genet. 2006 Jan 15;15(2):189-99. Epub 2005 Dec 1.
PMID: 16321991 [PubMed - in process]

39: Kimonis VE, Watts GD.
Autosomal dominant inclusion body myopathy, Paget disease of bone, and
frontotemporal dementia.
Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19 Suppl 1:S44-7.
PMID: 16317258 [PubMed - indexed for MEDLINE]

40: Fernandez C, Figarella-Branger D, Meyronet D, Cassote E, Tong S, Pellissier
JF.
Electron microscopy in neuromuscular disorders.
Ultrastruct Pathol. 2005 Nov-Dec;29(6):437-50. Review.
PMID: 16316944 [PubMed - indexed for MEDLINE]

41: Askanas V, Engel WK.
Sporadic inclusion-body myositis: a proposed key pathogenetic role of the
abnormalities of the ubiquitin-proteasome system, and protein misfolding and
aggregation.
Acta Myol. 2005 Jul;24(1):17-24.
PMID: 16315367 [PubMed - indexed for MEDLINE]

42: Maurage CA, Udd B, Ruchoux MM, Vermersch P, Kalimo H, Krahe R, Delacourte
A, Sergeant N.
Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease.
Neurology. 2005 Nov 22;65(10):1636-8.
PMID: 16301494 [PubMed - indexed for MEDLINE]

43: Schreiner B, Voss J, Wischhusen J, Dombrowski Y, Steinle A, Lochmuller H,
Dalakas M, Melms A, Wiendl H.
Expression of toll-like receptors by human muscle cells in vitro and in vivo:
TLR3 is highly expressed in inflammatory and HIV myopathies, mediates IL-8
release and up-regulation of NKG2D-ligands.
FASEB J. 2006 Jan;20(1):118-20. Epub 2005 Nov 17.
PMID: 16293707 [PubMed - indexed for MEDLINE]

44: Katirji B, Hachwi R, Al-Shekhlee A, Cohen ML, Bohlman HH.
Isolated dropped head due to adult-onset nemaline myopathy treated by posterior
fusion.
Neurology. 2005 Nov 8;65(9):1504-5. No abstract available.
PMID: 16275851 [PubMed - indexed for MEDLINE]

45: O'Hanlon TP, Carrick DM, Arnett FC, Reveille JD, Carrington M, Gao X, Oddis
CV, Morel PA, Malley JD, Malley K, Dreyfuss J, Shamim EA, Rider LG, Chanock SJ,
Foster CB, Bunch T, Plotz PH, Love LA, Miller FW.
Immunogenetic risk and protective factors for the idiopathic inflammatory
myopathies: distinct HLA-A, -B, -Cw, -DRB1 and -DQA1 allelic profiles and motifs
define clinicopathologic groups in caucasians.
Medicine (Baltimore). 2005 Nov;84(6):338-49.
PMID: 16267409 [PubMed - indexed for MEDLINE]

46: Haubenberger D, Bittner RE, Rauch-Shorny S, Zimprich F, Mannhalter C,
Wagner L, Mineva I, Vass K, Auff E, Zimprich A.
Inclusion body myopathy and Paget disease is linked to a novel mutation in the
VCP gene.
Neurology. 2005 Oct 25;65(8):1304-5.
PMID: 16247064 [PubMed - indexed for MEDLINE]

47: Rivas E, Gomez-Arnaiz M, Ricoy JR, Mateos F, Simon R, Garcia-Penas JJ,
Garcia-Silva MT, Martin E, Vazquez M, Ferreiro A, Cabello A.
Macrophagic myofasciitis in childhood: a controversial entity.
Pediatr Neurol. 2005 Nov;33(5):350-6.
PMID: 16243223 [PubMed - indexed for MEDLINE]

48: Wang Q, Mosser DD, Bag J.
Induction of HSP70 expression and recruitment of HSC70 and HSP70 in the nucleus
reduce aggregation of a polyalanine expansion mutant of PABPN1 in HeLa cells.
Hum Mol Genet. 2005 Dec 1;14(23):3673-84. Epub 2005 Oct 20.
PMID: 16239242 [PubMed - indexed for MEDLINE]

49: Sharma MC, Goebel HH.
Protein aggregate myopathies.
Neurol India. 2005 Sep;53(3):273-9. Review.
PMID: 16230791 [PubMed - indexed for MEDLINE]

50: Shi J, Shaw CL, Du Plessis D, Richardson AM, Bailey KL, Julien C, Stopford
C, Thompson J, Varma A, Craufurd D, Tian J, Pickering-Brown S, Neary D, Snowden
JS, Mann DM.
Histopathological changes underlying frontotemporal lobar degeneration with
clinicopathological correlation.
Acta Neuropathol (Berl). 2005 Nov;110(5):501-12. Epub 2005 Oct 13.
PMID: 16222525 [PubMed - in process]

51: Lucas GJ, Mehta SG, Hocking LJ, Stewart TL, Cundy T, Nicholson GC, Walsh
JP, Fraser WD, Watts GD, Ralston SH, Kimonis VE.
Evaluation of the role of Valosin-containing protein in the pathogenesis of
familial and sporadic Paget's disease of bone.
Bone. 2006 Feb;38(2):280-5. Epub 2005 Sep 30.
PMID: 16199218 [PubMed - in process]

52: Fidzianska A, Ryniewicz B, Shen XM, Engel AG.
IBM-type inclusions in a patient with slow-channel syndrome caused by a
mutation in the AChR epsilon subunit.
Neuromuscul Disord. 2005 Nov;15(11):753-9. Epub 2005 Sep 28.
PMID: 16198106 [PubMed - indexed for MEDLINE]

53: Tian L, Greenberg SA, Kong SW, Altschuler J, Kohane IS, Park PJ.
Discovering statistically significant pathways in expression profiling studies.
Proc Natl Acad Sci U S A. 2005 Sep 20;102(38):13544-9. Epub 2005 Sep 8.
PMID: 16174746 [PubMed - indexed for MEDLINE]

54: Mastaglia FL, Lamont PJ, Laing NG.
Distal myopathies.
Curr Opin Neurol. 2005 Oct;18(5):504-10. Review.
PMID: 16155432 [PubMed - indexed for MEDLINE]

55: Oldfors A, Lindberg C.
Diagnosis, pathogenesis and treatment of inclusion body myositis.
Curr Opin Neurol. 2005 Oct;18(5):497-503. Review.
PMID: 16155431 [PubMed - indexed for MEDLINE]

56: Chahin N, Selcen D, Engel AG.
Sporadic late onset nemaline myopathy.
Neurology. 2005 Oct 25;65(8):1158-64. Epub 2005 Sep 7.
PMID: 16148261 [PubMed - indexed for MEDLINE]

57: Engvall M, Ahlberg G, Hedberg B, Edstrom L, Ansved T.
Sarcoplasmic body myopathy--a rare hereditary myopathy with characteristic
inclusions.
Acta Neurol Scand. 2005 Oct;112(4):223-7.
PMID: 16146490 [PubMed - indexed for MEDLINE]

58: Rao PV, Lu X, Pattee P, Turner M, Nandgaonkar S, Paturi BT, Roberts CT Jr,
Nagalla SR.
Peripheral genotype-phenotype correlations in Asian Indians with type 2
diabetes mellitus.
J Assoc Physicians India. 2005 Jun;53:521-6.
PMID: 16121806 [PubMed - indexed for MEDLINE]

59: Shinchuk LM, Sharma D, Blondelle SE, Reixach N, Inouye H, Kirschner DA.
Poly-(L-alanine) expansions form core beta-sheets that nucleate amyloid
assembly.
Proteins. 2005 Nov 15;61(3):579-89.
PMID: 16114037 [PubMed - indexed for MEDLINE]

60: Gottlieb E, Ciccone C, Darvish D, Naiem-Cohen S, Dalakas MC, Savelkoul PJ,
Krasnewich DM, Gahl WA, Huizing M.
Single nucleotide polymorphisms in the dystroglycan gene do not correlate with
disease severity in hereditary inclusion body myopathy.
Mol Genet Metab. 2005 Sep-Oct;86(1-2):244-9.
PMID: 16112887 [PubMed - indexed for MEDLINE]

61: Schwarzmeier JD, Hamwi A, Preisel M, Resl C, Preusser M, Sluga E, Horcher
E, Shehata MM.
Positive troponin T without cardiac involvement in inclusion body myositis.
Hum Pathol. 2005 Aug;36(8):917-21.
PMID: 16112010 [PubMed - indexed for MEDLINE]

62: Daroszewska A, Ralston SH.
Genetics of Paget's disease of bone.
Clin Sci (Lond). 2005 Sep;109(3):257-63. Review.
PMID: 16104845 [PubMed - indexed for MEDLINE]

63: Askanas V, Engel WK.
Molecular pathology and pathogenesis of inclusion-body myositis.
Microsc Res Tech. 2005 Jul;67(3-4):114-20. Review.
PMID: 16104000 [PubMed - indexed for MEDLINE]

64: Abu-Baker A, Laganiere S, Fan X, Laganiere J, Brais B, Rouleau GA.
Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses
protein aggregation and toxicity in oculopharyngeal muscular dystrophy.
Traffic. 2005 Sep;6(9):766-79.
PMID: 16101680 [PubMed - indexed for MEDLINE]

65: Nakano S, Shinde A, Ito H, Ito H, Kusaka H.
Messenger RNA degradation may be inhibited in sporadic inclusion body myositis.
Neurology. 2005 Aug 9;65(3):420-5.
PMID: 16087907 [PubMed - indexed for MEDLINE]

66: Fratta P, Engel WK, McFerrin J, Davies KJ, Lin SW, Askanas V.
Proteasome inhibition and aggresome formation in sporadic inclusion-body
myositis and in amyloid-beta precursor protein-overexpressing cultured human
muscle fibers.
Am J Pathol. 2005 Aug;167(2):517-26.
PMID: 16049336 [PubMed - indexed for MEDLINE]

67: Choy EH, Hoogendijk JE, Lecky B, Winer JB.
Immunosuppressant and immunomodulatory treatment for dermatomyositis and
polymyositis.
Cochrane Database Syst Rev. 2005 Jul 20;(3):CD003643. Review.
PMID: 16034905 [PubMed - indexed for MEDLINE]

68: Rafay MF, Halliday W, Bril V.
Hyaline body myopathy: adulthood manifestations.
Can J Neurol Sci. 2005 May;32(2):253-6.
PMID: 16018165 [PubMed - indexed for MEDLINE]

69: Sparks SE, Ciccone C, Lalor M, Orvisky E, Klootwijk R, Savelkoul PJ,
Dalakas MC, Krasnewich DM, Gahl WA, Huizing M.
Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and
N-acetylmannosamine kinase activities in human hereditary inclusion body
myopathy.
Glycobiology. 2005 Nov;15(11):1102-10. Epub 2005 Jun 29.
PMID: 15987957 [PubMed - indexed for MEDLINE]

70: Sharma MC, Schultze C, von Moers A, Stoltenburg-Didinger G, Shin YS,
Podskarbi T, Isenhardt K, Tews DS, Goebel HH.
Delayed or late-onset type II glycogenosis with globular inclusions.
Acta Neuropathol (Berl). 2005 Aug;110(2):151-7. Epub 2005 Jun 29.
PMID: 15986226 [PubMed - indexed for MEDLINE]

71: Wojcik S, Engel WK, McFerrin J, Askanas V.
Myostatin is increased and complexes with amyloid-beta within sporadic
inclusion-body myositis muscle fibers.
Acta Neuropathol (Berl). 2005 Aug;110(2):173-7. Epub 2005 Jun 28.
PMID: 15983828 [PubMed - indexed for MEDLINE]

72: Tseng BP, Kitazawa M, LaFerla FM.
Amyloid beta-peptide: the inside story.
Curr Alzheimer Res. 2004 Nov;1(4):231-9. Review.
PMID: 15975052 [PubMed - indexed for MEDLINE]

73: Illa I.
IVIg in myasthenia gravis, Lambert Eaton myasthenic syndrome and inflammatory
myopathies: current status.
J Neurol. 2005 May;252 Suppl 1:I14-8. Review.
PMID: 15959667 [PubMed - indexed for MEDLINE]

74: Sugarman MC, Kitazawa M, Baker M, Caiozzo VJ, Querfurth HW, LaFerla FM.
Pathogenic accumulation of APP in fast twitch muscle of IBM patients and a
transgenic model.
Neurobiol Aging. 2006 Mar;27(3):423-32. Epub 2005 Jun 13.
PMID: 15950323 [PubMed - indexed for MEDLINE]

75: Miladi MI, Feki I, Choyakh F, Ben Hmida M, Zouari N, Mhiri C.
Polysaccharide storage myopathy--case report and literature review.
Clin Neuropathol. 2005 May-Jun;24(3):126-32. Review.
PMID: 15943164 [PubMed - indexed for MEDLINE]

76: De Paepe B, De Keyzer K, Martin JJ, De Bleecker JL.
Alpha-chemokine receptors CXCR1-3 and their ligands in idiopathic inflammatory
myopathies.
Acta Neuropathol (Berl). 2005 Jun;109(6):576-82. Epub 2005 Jun 4.
PMID: 15937690 [PubMed - indexed for MEDLINE]

77: Ferrer I, Carmona M, Blanco R, Moreno D, Torrejon-Escribano B, Olive M.
Involvement of clusterin and the aggresome in abnormal protein deposits in
myofibrillar myopathies and inclusion body myositis.
Brain Pathol. 2005 Apr;15(2):101-8.
PMID: 15912881 [PubMed - indexed for MEDLINE]

78: Authier FJ, Chariot P, Gherardi RK.
Skeletal muscle involvement in human immunodeficiency virus (HIV)-infected
patients in the era of highly active antiretroviral therapy (HAART).
Muscle Nerve. 2005 Sep;32(3):247-60. Review.
PMID: 15902690 [PubMed - indexed for MEDLINE]

79: Amoura Z, Duhaut P, Huong du LT, Wechsler B, Costedoat-Chalumeau N, Frances
C, Cacoub P, Papo T, Cormont S, Touitou Y, Grenier P, Valeyre D, Piette JC.
Tumor antigen markers for the detection of solid cancers in inflammatory
myopathies.
Cancer Epidemiol Biomarkers Prev. 2005 May;14(5):1279-82.
PMID: 15894686 [PubMed - indexed for MEDLINE]

80: Behnam K, Murray SS, Brochmann EJ.
Identification and characterization of valosin-containing protein (VCP/p97) in
untransformed osteoblast-like cells.
J Orthop Res. 2005 May;23(3):618-24. Epub 2005 Apr 19.
PMID: 15885483 [PubMed - indexed for MEDLINE]

81: Raju R, Dalakas MC.
Gene expression profile in the muscles of patients with inflammatory
myopathies: effect of therapy with IVIg and biological validation of clinically
relevant genes.
Brain. 2005 Aug;128(Pt 8):1887-96. Epub 2005 Apr 27.
PMID: 15857930 [PubMed - indexed for MEDLINE]

82: Greenberg SA, Pinkus JL, Pinkus GS, Burleson T, Sanoudou D, Tawil R, Barohn
RJ, Saperstein DS, Briemberg HR, Ericsson M, Park P, Amato AA.
Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis.
Ann Neurol. 2005 May;57(5):664-78.
PMID: 15852401 [PubMed - indexed for MEDLINE]

83: Amouri R, Driss A, Murayama K, Kefi M, Nishino I, Hentati F.
Allelic heterogeneity of GNE gene mutation in two Tunisian families with
autosomal recessive inclusion body myopathy.
Neuromuscul Disord. 2005 May;15(5):361-3.
PMID: 15833430 [PubMed - indexed for MEDLINE]

84: Krivickas LS, Amato AA, Krishnan G, Murray AV, Frontera WR.
Preservation of in vitro muscle fiber function in dermatomyositis and inclusion
body myositis: a single fiber study.
Neuromuscul Disord. 2005 May;15(5):349-54.
PMID: 15833427 [PubMed - indexed for MEDLINE]

85: Nardin R.
Personal history: resolution.
Neurology. 2005 Apr 12;64(7):1315-6. No abstract available.
PMID: 15824380 [PubMed - indexed for MEDLINE]

86: Alexandrescu DT, Bhagwati NS, Fomberstein B, Wolfe DE, Feliz A, Wiernik PH.

Steroid-responsive inclusion body myositis associated with endometrial cancer.
Clin Exp Rheumatol. 2005 Jan-Feb;23(1):93-6. Review.
PMID: 15789894 [PubMed - indexed for MEDLINE]

87: Fidzianska A, Kaminska A, Ryniewicz B.
Congenital myopathy with tubular aggregates and tubulofilamentous IBM-type
inclusions.
Neuropediatrics. 2005 Feb;36(1):35-9.
PMID: 15776320 [PubMed - indexed for MEDLINE]

88: De Paepe B, De Bleecker JL.
Beta-chemokine receptor expression in idiopathic inflammatory myopathies.
Muscle Nerve. 2005 May;31(5):621-7.
PMID: 15772970 [PubMed - indexed for MEDLINE]

89: Ranque-Francois B, Maisonobe T, Dion E, Piette JC, Chauveheid MP, Amoura Z,
Papo T.
Familial inflammatory inclusion body myositis.
Ann Rheum Dis. 2005 Apr;64(4):634-7. Review.
PMID: 15769920 [PubMed - indexed for MEDLINE]

90: Alexanderson H.
Exercise: an important component of treatment in the idiopathic inflammatory
myopathies.
Curr Rheumatol Rep. 2005 Apr;7(2):115-24. Review.
PMID: 15760590 [PubMed - indexed for MEDLINE]

91: Corbeil-Girard LP, Klein AF, Sasseville AM, Lavoie H, Dicaire MJ,
Saint-Denis A, Page M, Duranceau A, Codere F, Bouchard JP, Karpati G, Rouleau
GA, Massie B, Langelier Y, Brais B.
PABPN1 overexpression leads to upregulation of genes encoding nuclear proteins
that are sequestered in oculopharyngeal muscular dystrophy nuclear inclusions.
Neurobiol Dis. 2005 Apr;18(3):551-67.
PMID: 15755682 [PubMed - indexed for MEDLINE]

92: Gendek EG, Kedziora J, Gendek-Kubiak H.
Can tissue transglutaminase be a marker of idiopathic inflammatory myopathies?
Immunol Lett. 2005 Mar 15;97(2):245-9. Epub 2004 Dec 13.
PMID: 15752564 [PubMed - indexed for MEDLINE]

93: Krause S, Hinderlich S, Amsili S, Horstkorte R, Wiendl H, Argov Z,
Mitrani-Rosenbaum S, Lochmuller H.
Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex
and the nucleus of mammalian cells.
Exp Cell Res. 2005 Apr 1;304(2):365-79. Epub 2004 Dec 19.
PMID: 15748884 [PubMed - indexed for MEDLINE]

94: Lynn SJ, Sawyers SM, Moller PW, O'Donnell JL, Chapman PT.
Adult-onset inflammatory myopathy: North Canterbury experience 1989-2001.
Intern Med J. 2005 Mar;35(3):170-3.
PMID: 15737137 [PubMed - indexed for MEDLINE]

95: Schroder R, Watts GD, Mehta SG, Evert BO, Broich P, Fliessbach K, Pauls K,
Hans VH, Kimonis V, Thal DR.
Mutant valosin-containing protein causes a novel type of frontotemporal
dementia.
Ann Neurol. 2005 Mar;57(3):457-61.
PMID: 15732117 [PubMed - indexed for MEDLINE]

96: Alexanderson H, Lundberg IE.
The role of exercise in the rehabilitation of idiopathic inflammatory
myopathies.
Curr Opin Rheumatol. 2005 Mar;17(2):164-71. Review.
PMID: 15711230 [PubMed - indexed for MEDLINE]

97: Oldfors A, Tajsharghi H, Thornell LE.
Mutation of the slow myosin heavy chain rod domain underlies hyaline body
myopathy.
Neurology. 2005 Feb 8;64(3):580-1; author reply 580-1. Review. No abstract
available.
PMID: 15699411 [PubMed - indexed for MEDLINE]

98: Laing NG, Ceuterick-de Groote C, Dye DE, Liyanage K, Duff RM, Dubois B,
Robberecht W, Sciot R, Martin JJ, Goebel HH.
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated
cases.
Neurology. 2005 Feb 8;64(3):527-9.
PMID: 15699387 [PubMed - indexed for MEDLINE]

99: Cafforio G, Pistolesi S, D'Avino C, Galluzzi F, Patricelli A, Solito B,
Fontanini G, Siciliano G.
Inclusion body myopathy associated with motor neuron syndrome: three case
reports.
Clin Neuropathol. 2005 Jan-Feb;24(1):36-41.
PMID: 15696783 [PubMed - indexed for MEDLINE]

100: Broccolini A, Gliubizzi C, Pavoni E, Gidaro T, Morosetti R, Sciandra F,
Giardina B, Tonali P, Ricci E, Brancaccio A, Mirabella M.
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive
hereditary inclusion-body myopathy.
Neuromuscul Disord. 2005 Feb;15(2):177-84. Epub 2004 Dec 10.
PMID: 15694140 [PubMed - indexed for MEDLINE]

101: Nonaka I, Noguchi S, Nishino I.
Distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy.
Curr Neurol Neurosci Rep. 2005 Feb;5(1):61-5. Review.
PMID: 15676110 [PubMed - indexed for MEDLINE]

102: Salama I, Hinderlich S, Shlomai Z, Eisenberg I, Krause S, Yarema K, Argov
Z, Lochmuller H, Reutter W, Dabby R, Sadeh M, Ben-Bassat H, Mitrani-Rosenbaum S.

No overall hyposialylation in hereditary inclusion body myopathy myoblasts
carrying the homozygous M712T GNE mutation.
Biochem Biophys Res Commun. 2005 Mar 4;328(1):221-6.
PMID: 15670773 [PubMed - indexed for MEDLINE]

103: Takamure M, Murata KY, Kawahara M, Ueno S.
Finger flexor weakness in inclusion body myositis.
Neurology. 2005 Jan 25;64(2):389. No abstract available.
PMID: 15668452 [PubMed - indexed for MEDLINE]

104: Cantwell C, Ryan M, O'Connell M, Cunningham P, Brennan D, Costigan D,
Lynch T, Eustace S.
A comparison of inflammatory myopathies at whole-body turbo STIR MRI.
Clin Radiol. 2005 Feb;60(2):261-7. No abstract available.
PMID: 15664582 [PubMed - indexed for MEDLINE]

105: Cherin P.
Inflammatory myopathies.
Acta Clin Belg. 2004 Sep-Oct;59(5):290-9. Review. No abstract available.
PMID: 15641400 [PubMed - indexed for MEDLINE]

106: Teixeira A, Cherin P, Demoule A, Levy-Soussan M, Straus C, Verin E, Zelter
M, Derenne JP, Herson S, Similowski T.
Diaphragmatic dysfunction in patients with idiopathic inflammatory myopathies.
Neuromuscul Disord. 2005 Jan;15(1):32-9.
PMID: 15639118 [PubMed - indexed for MEDLINE]

107: Civatte M, Bartoli C, Schleinitz N, Chetaille B, Pellissier JF,
Figarella-Branger D.
Expression of the beta chemokines CCL3, CCL4, CCL5 and their receptors in
idiopathic inflammatory myopathies.
Neuropathol Appl Neurobiol. 2005 Feb;31(1):70-9.
PMID: 15634233 [PubMed - indexed for MEDLINE]

108: Badrising UA, Schreuder GM, Giphart MJ, Geleijns K, Verschuuren JJ,
Wintzen AR, Maat-Schieman ML, van Doorn P, van Engelen BG, Faber CG, Hoogendijk
JE, de Jager AE, Koehler PJ, de Visser M, van Duinen SG; Dutch IBM Study Group.
Associations with autoimmune disorders and HLA class I and II antigens in
inclusion body myositis.
Neurology. 2004 Dec 28;63(12):2396-8.
PMID: 15623710 [PubMed - indexed for MEDLINE]

109: Mastaglia FL.
Neuromuscular disorders: molecular and therapeutic insights.
Lancet Neurol. 2005 Jan;4(1):6-7. Review. No abstract available.
PMID: 15620848 [PubMed - indexed for MEDLINE]

110: Oldfors A, Tajsharghi H, Darin N, Lindberg C.
Myopathies associated with myosin heavy chain mutations.
Acta Myol. 2004 Sep;23(2):90-6. Review.
PMID: 15605950 [PubMed - indexed for MEDLINE]

111: Muntoni F.
Journey into muscular dystrophies caused by abnormal glycosylation.
Acta Myol. 2004 Sep;23(2):79-84. Review.
PMID: 15605948 [PubMed - indexed for MEDLINE]

112: Voermans NC, Vaneker M, Hengstman GJ, ter Laak HJ, Zimmerman C, Schelhaas
HJ, Zwarts MJ.
Primary respiratory failure in inclusion body myositis.
Neurology. 2004 Dec 14;63(11):2191-2. Review. No abstract available.
PMID: 15596785 [PubMed - indexed for MEDLINE]

113: Chinoy H, Ollier WE, Cooper RG.
Have recent immunogenetic investigations increased our understanding of disease
mechanisms in the idiopathic inflammatory myopathies?
Curr Opin Rheumatol. 2004 Nov;16(6):707-13. Review.
PMID: 15577608 [PubMed - indexed for MEDLINE]

114: Christopher-Stine L, Plotz PH.
Myositis: an update on pathogenesis.
Curr Opin Rheumatol. 2004 Nov;16(6):700-6. Review.
PMID: 15577607 [PubMed - indexed for MEDLINE]

115: Nirmalananthan N, Holton JL, Hanna MG.
Is it really myositis? A consideration of the differential diagnosis.
Curr Opin Rheumatol. 2004 Nov;16(6):684-91. Review.
PMID: 15577605 [PubMed - indexed for MEDLINE]

116: Lossos A, Baala L, Soffer D, Averbuch-Heller L, Dotan S, Munnich A,
Lyonnet S, Gomori JM, Genem A, Neufeld M, Abramsky O, Zlotogora J, Argov Z.
A novel autosomal recessive myopathy with external ophthalmoplegia linked to
chromosome 17p13.1-p12.
Brain. 2005 Jan;128(Pt 1):42-51. Epub 2004 Nov 17.
PMID: 15548556 [PubMed - indexed for MEDLINE]

117: Maurage CA, Bussiere T, Sergeant N, Ghesteem A, Figarella-Branger D,
Ruchoux MM, Pellissier JF, Delacourte A.
Tau aggregates are abnormally phosphorylated in inclusion body myositis and
have an immunoelectrophoretic profile distinct from other tauopathies.
Neuropathol Appl Neurobiol. 2004 Dec;30(6):624-34.
PMID: 15541003 [PubMed - indexed for MEDLINE]

118: Price P, Santoso L, Mastaglia F, Garlepp M, Kok CC, Allcock R, Laing N.
Two major histocompatibility complex haplotypes influence susceptibility to
sporadic inclusion body myositis: critical evaluation of an association with
HLA-DR3.
Tissue Antigens. 2004 Nov;64(5):575-80.
PMID: 15496200 [PubMed - indexed for MEDLINE]

119: Kovacs GG, Kalev O, Gelpi E, Haberler C, Wanschitz J, Strohschneider M,
Molnar MJ, Laszlo L, Budka H.
The prion protein in human neuromuscular diseases.
J Pathol. 2004 Nov;204(3):241-7.
PMID: 15476279 [PubMed - indexed for MEDLINE]

120: Fratta P, Engel WK, Van Leeuwen FW, Hol EM, Vattemi G, Askanas V.
Mutant ubiquitin UBB+1 is accumulated in sporadic inclusion-body myositis
muscle fibers.
Neurology. 2004 Sep 28;63(6):1114-7.
PMID: 15452314 [PubMed - indexed for MEDLINE]

121: Shahrizaila N, Lowe J, Wills A.
Familial myopathy with tubular aggregates associated with abnormal pupils.
Neurology. 2004 Sep 28;63(6):1111-3.
PMID: 15452313 [PubMed - indexed for MEDLINE]

122: Krishnan AV, Pamphlett R, Burke D, Wills EJ, Kiernan MC.
Cytoplasmic body myopathy masquerading as motor neuron disease.
Muscle Nerve. 2004 Nov;30(5):667-72.
PMID: 15389660 [PubMed - indexed for MEDLINE]

123: Kleopa KA, Kyriacou K, Zamba-Papanicolaou E, Kyriakides T.
Reversible inflammatory and vacuolar myopathy with vitamin E deficiency in
celiac disease.
Muscle Nerve. 2005 Feb;31(2):260-5.
PMID: 15389648 [PubMed - indexed for MEDLINE]

124: Dalakas MC.
Inflammatory disorders of muscle: progress in polymyositis, dermatomyositis and
inclusion body myositis.
Curr Opin Neurol. 2004 Oct;17(5):561-7. Review.
PMID: 15367860 [PubMed - indexed for MEDLINE]

125: Bonnemann CG, Laing NG.
Myopathies resulting from mutations in sarcomeric proteins.
Curr Opin Neurol. 2004 Oct;17(5):529-37. Review.
PMID: 15367857 [PubMed - indexed for MEDLINE]

126: Haliloglu G, Topaloglu H.
Glycosylation defects in muscular dystrophies.
Curr Opin Neurol. 2004 Oct;17(5):521-7. Review.
PMID: 15367856 [PubMed - indexed for MEDLINE]

127: Ozden S, Cochet M, Mikol J, Teixeira A, Gessain A, Pique C.
Direct evidence for a chronic CD8+-T-cell-mediated immune reaction to tax
within the muscle of a human T-cell leukemia/lymphoma virus type 1-infected
patient with sporadic inclusion body myositis.
J Virol. 2004 Oct;78(19):10320-7.
PMID: 15367598 [PubMed - indexed for MEDLINE]

128: Muscle Study Group.
Randomized pilot trial of high-dose betaINF-1a in patients with inclusion body
myositis.
Neurology. 2004 Aug 24;63(4):718-20.
PMID: 15326251 [PubMed - indexed for MEDLINE]

129: Yakushiji Y, Satoh J, Yukitake M, Yamaguchi K, Nakamura I, Nishino I,
Kuroda Y.
Interferon beta-responsive inclusion body myositis in a hepatitis C virus
carrier.
Neurology. 2004 Aug 10;63(3):587-8. No abstract available.
PMID: 15304605 [PubMed - indexed for MEDLINE]

130: Hengstman GJ, van Engelen BG.
Polymyositis: an overdiagnosed entity.
Neurology. 2004 Jul 27;63(2):402-3; author reply 403. No abstract available.
PMID: 15282847 [PubMed - indexed for MEDLINE]

131: Bradley WG.
Polymyositis: an overdiagnosed entity.
Neurology. 2004 Jul 27;63(2):402; author reply 403. No abstract available.
PMID: 15282846 [PubMed - indexed for MEDLINE]

132: Askanas V, Engel WK.
Unicorns, dragons, polymyositis, and other mythical beasts.
Neurology. 2004 Jul 27;63(2):403-4; author reply 404. No abstract available.
PMID: 15277658 [PubMed - indexed for MEDLINE]

133: Strazielle C, Dumont M, Fukuchi K, Lalonde R.
Transgenic mice expressing the human C99 terminal fragment of betaAPP: effects
on cytochrome oxidase activity in skeletal muscle and brain.
J Chem Neuroanat. 2004 Jul;27(4):237-46.
PMID: 15261330 [PubMed - indexed for MEDLINE]

134: Probst-Cousin S, Berghoff C, Neundorfer B, Heuss D.
Annexin expression in inflammatory myopathies.
Muscle Nerve. 2004 Jul;30(1):102-10.
PMID: 15221885 [PubMed - indexed for MEDLINE]

135: Neudecker S, Krasnianski M, Bahn E, Zierz S.
Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique
ultrastructural feature.
Acta Neuropathol (Berl). 2004 Sep;108(3):257-9. Epub 2004 Jun 24.
PMID: 15221332 [PubMed - indexed for MEDLINE]

136: Schroder JM, Durling H, Laing N.
Actin myopathy with nemaline bodies, intranuclear rods, and a heterozygous
mutation in ACTA1 (Asp154Asn).
Acta Neuropathol (Berl). 2004 Sep;108(3):250-6. Epub 2004 Jun 24.
PMID: 15221331 [PubMed - indexed for MEDLINE]

137: Broccolini A, Ricci E, Pescatori M, Papacci M, Gliubizzi C, D'Amico A,
Servidei S, Tonali P, Mirabella M.
Insulin-like growth factor I in inclusion-body myositis and human muscle
cultures.
J Neuropathol Exp Neurol. 2004 Jun;63(6):650-9.
PMID: 15217093 [PubMed - indexed for MEDLINE]

138: Ferrer I, Martin B, Castano JG, Lucas JJ, Moreno D, Olive M.
Proteasomal expression, induction of immunoproteasome subunits, and local MHC
class I presentation in myofibrillar myopathy and inclusion body myositis.
J Neuropathol Exp Neurol. 2004 May;63(5):484-98.
PMID: 15198127 [PubMed - indexed for MEDLINE]

139: Liu LW, Tarnopolsky M, Armstrong D.
Injection of botulinum toxin A to the upper esophageal sphincter for
oropharyngeal dysphagia in two patients with inclusion body myositis.
Can J Gastroenterol. 2004 Jun;18(6):397-9.
PMID: 15190396 [PubMed - indexed for MEDLINE]

140: Dalakas MC.
The molecular pathophysiology in inflammatory myopathies.
Rev Med Interne. 2004 Jun;25 Suppl 1:S14-6. Review. No abstract available.
PMID: 15165685 [PubMed - indexed for MEDLINE]

141: Gossrau G, Gestrich B, Koch R, Wunderlich C, Schroder JM, Schroeder S,
Reichmann H, Lampe JB.
Apolipoprotein E and alpha-1-antichymotrypsin polymorphisms in sporadic
inclusion body myositis.
Eur Neurol. 2004;51(4):215-20. Epub 2004 May 17.
PMID: 15159602 [PubMed - indexed for MEDLINE]

142: Wedderburn LR, Li CK.
Paediatric idiopathic inflammatory muscle disease.
Best Pract Res Clin Rheumatol. 2004 Jun;18(3):345-58. Review.
PMID: 15158745 [PubMed - indexed for MEDLINE]

143: Christopher-Stine L, Plotz PH.
Adult inflammatory myopathies.
Best Pract Res Clin Rheumatol. 2004 Jun;18(3):331-44. Review.
PMID: 15158744 [PubMed - indexed for MEDLINE]

144: Hinderlich S, Salama I, Eisenberg I, Potikha T, Mantey LR, Yarema KJ,
Horstkorte R, Argov Z, Sadeh M, Reutter W, Mitrani-Rosenbaum S.
The homozygous M712T mutation of UDP-N-acetylglucosamine
2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but
not in altered overall cellular sialylation in hereditary inclusion body
myopathy.
FEBS Lett. 2004 May 21;566(1-3):105-9.
PMID: 15147877 [PubMed - indexed for MEDLINE]

145: Broccolini A, Ricci E, Cassandrini D, Gliubizzi C, Bruno C, Tonoli E,
Silvestri G, Pescatori M, Rodolico C, Sinicropi S, Servidei S, Zara F, Minetti
C, Tonali PA, Mirabella M.
Novel GNE mutations in Italian families with autosomal recessive hereditary
inclusion-body myopathy.
Hum Mutat. 2004 Jun;23(6):632.
PMID: 15146476 [PubMed - indexed for MEDLINE]

146: Arnardottir S, Borg K, Ansved T.
Sporadic inclusion body myositis: morphology, regeneration, and cytoskeletal
structure of muscle fibres.
J Neurol Neurosurg Psychiatry. 2004 Jun;75(6):917-20.
PMID: 15146016 [PubMed - indexed for MEDLINE]

147: De Paepe B, Racz GZ, Schroder JM, De Bleecker JL.
Expression and distribution of the nitric oxide synthases in idiopathic
inflammatory myopathies.
Acta Neuropathol (Berl). 2004 Jul;108(1):37-42. Epub 2004 May 8.
PMID: 15138776 [PubMed - indexed for MEDLINE]

148: Tomimitsu H, Shimizu J, Ishikawa K, Ohkoshi N, Kanazawa I, Mizusawa H.
Distal myopathy with rimmed vacuoles (DMRV): new GNE mutations and splice
variant.
Neurology. 2004 May 11;62(9):1607-10.
PMID: 15136692 [PubMed - indexed for MEDLINE]

149: Bohlega S, Abu-Amero SN, Wakil SM, Carroll P, Al-Amr R, Lach B, Al-Sayed
Y, Cupler EJ, Meyer BF.
Mutation of the slow myosin heavy chain rod domain underlies hyaline body
myopathy.
Neurology. 2004 May 11;62(9):1518-21.
PMID: 15136674 [PubMed - indexed for MEDLINE]

150: Blume A, Ghaderi D, Liebich V, Hinderlich S, Donner P, Reutter W, Lucka L.

UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, functionally
expressed in and purified from Escherichia coli, yeast, and insect cells.
Protein Expr Purif. 2004 Jun;35(2):387-96.
PMID: 15135418 [PubMed - indexed for MEDLINE]

151: Minamiyama M, Katsuno M, Adachi H, Waza M, Sang C, Kobayashi Y, Tanaka F,
Doyu M, Inukai A, Sobue G.
Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model
of spinal and bulbar muscular atrophy.
Hum Mol Genet. 2004 Jun 1;13(11):1183-92. Epub 2004 Apr 21.
PMID: 15102712 [PubMed - indexed for MEDLINE]

152: Hoogendijk JE, Amato AA, Lecky BR, Choy EH, Lundberg IE, Rose MR,
Vencovsky J, de Visser M, Hughes RA.
119th ENMC international workshop: trial design in adult idiopathic
inflammatory myopathies, with the exception of inclusion body myositis, 10-12
October 2003, Naarden, The Netherlands.
Neuromuscul Disord. 2004 May;14(5):337-45. No abstract available.
PMID: 15099594 [PubMed - indexed for MEDLINE]

153: De Bleecker J, Vervaet V, Van den Bergh P.
Necrotizing myopathy with microvascular deposition of the complement membrane
attack complex.
Clin Neuropathol. 2004 Mar-Apr;23(2):76-9.
PMID: 15074581 [PubMed - indexed for MEDLINE]

154: Tarnopolsky MA, Simon DK, Roy BD, Chorneyko K, Lowther SA, Johns DR,
Sandhu JK, Li Y, Sikorska M.
Attenuation of free radical production and paracrystalline inclusions by
creatine supplementation in a patient with a novel cytochrome b mutation.
Muscle Nerve. 2004 Apr;29(4):537-47.
PMID: 15052619 [PubMed - indexed for MEDLINE]

155: Schmidt J, Rakocevic G, Raju R, Dalakas MC.
Upregulated inducible co-stimulator (ICOS) and ICOS-ligand in inclusion body
myositis muscle: significance for CD8+ T cell cytotoxicity.
Brain. 2004 May;127(Pt 5):1182-90. Epub 2004 Mar 26.
PMID: 15047591 [PubMed - indexed for MEDLINE]

156: Watts GD, Wymer J, Kovach MJ, Mehta SG, Mumm S, Darvish D, Pestronk A,
Whyte MP, Kimonis VE.
Inclusion body myopathy associated with Paget disease of bone and
frontotemporal dementia is caused by mutant valosin-containing protein.
Nat Genet. 2004 Apr;36(4):377-81. Epub 2004 Mar 21.
PMID: 15034582 [PubMed - indexed for MEDLINE]

157: Pezzoli G, Canesi M, Galli C.
An overview of parkinsonian syndromes: data from the literature and from an
Italian data-base.
Sleep Med. 2004 Mar;5(2):181-7. Review.
PMID: 15033141 [PubMed - indexed for MEDLINE]

158: De Paepe B, Schroder JM, Martin JJ, Racz GZ, De Bleecker JL.
Localization of the alpha-chemokine SDF-1 and its receptor CXCR4 in idiopathic
inflammatory myopathies.
Neuromuscul Disord. 2004 Apr;14(4):265-73.
PMID: 15019705 [PubMed - indexed for MEDLINE]

159: Nevo Y, Kutai M, Jossiphov J, Livne A, Neeman Z, Arad T, Popovitz-Biro R,
Atsmon J, Shapira Y, Soffer D.
Childhood macrophagic myofasciitis-consanguinity and clinicopathological
features.
Neuromuscul Disord. 2004 Apr;14(4):246-52.
PMID: 15019702 [PubMed - indexed for MEDLINE]

160: Nakamura A, Yoshida K, Ikeda S.
Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed
vacuoles.
Clin Neurol Neurosurg. 2004 Mar;106(2):122-8.
PMID: 15003303 [PubMed - indexed for MEDLINE]

161: Bornemann A, Bohl J, Schneider HM, Goebel HH, Schmidt PF, Gherardi RK.
July 2003: 62-year-old female with progressive muscular weakness.
Brain Pathol. 2004 Jan;14(1):109-10, 115.
PMID: 14997943 [PubMed - indexed for MEDLINE]

162: Gambelli S, Malandrini A, Ginanneschi F, Berti G, Cardaioli E, De Stefano
R, Franci M, Salvadori C, Mari F, Bruttini M, Rossi A, Federico A, Renieri A.
Mitochondrial abnormalities in genetically assessed oculopharyngeal muscular
dystrophy.
Eur Neurol. 2004;51(3):144-7. Epub 2004 Feb 27.
PMID: 14988608 [PubMed - indexed for MEDLINE]

163: Ikezoe K, Nakagawa M, Osoegawa M, Kira J, Nonaka I.
Ultrastructural detection of DNA fragmentation in myonuclei of fatal reducing
body myopathy.
Acta Neuropathol (Berl). 2004 May;107(5):439-42. Epub 2004 Feb 18.
PMID: 14986028 [PubMed - indexed for MEDLINE]

164: Berciano MT, Villagra NT, Ojeda JL, Navascues J, Gomes A, Lafarga M,
Carmo-Fonseca M.
Oculopharyngeal muscular dystrophy-like nuclear inclusions are present in
normal magnocellular neurosecretory neurons of the hypothalamus.
Hum Mol Genet. 2004 Apr 15;13(8):829-38. Epub 2004 Feb 19.
PMID: 14976164 [PubMed - indexed for MEDLINE]

165: Huizing M, Rakocevic G, Sparks SE, Mamali I, Shatunov A, Goldfarb L,
Krasnewich D, Gahl WA, Dalakas MC.
Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to
GNE mutations.
Mol Genet Metab. 2004 Mar;81(3):196-202.
PMID: 14972325 [PubMed - indexed for MEDLINE]

166: Fathi M, Dastmalchi M, Rasmussen E, Lundberg IE, Tornling G.
Interstitial lung disease, a common manifestation of newly diagnosed
polymyositis and dermatomyositis.
Ann Rheum Dis. 2004 Mar;63(3):297-301.
PMID: 14962966 [PubMed - indexed for MEDLINE]

167: Olive M, Unzeta M, Moreno D, Ferrer I.
Overexpression of semicarbazide-sensitive amine oxidase in human myopathies.
Muscle Nerve. 2004 Feb;29(2):261-6.
PMID: 14755492 [PubMed - indexed for MEDLINE]

168: Gherardi RK, Authier FJ.
Aluminum inclusion macrophagic myofasciitis: a recently identified condition.
Immunol Allergy Clin North Am. 2003 Nov;23(4):699-712. Review.
PMID: 14753387 [PubMed - indexed for MEDLINE]

169: Shinde A, Nakano S, Kusaka H, Nakaya Y, Sawada H, Kohara N, Shibasaki H.
Nucleolar characteristics of reducing bodies in reducing body myopathy.
Acta Neuropathol (Berl). 2004 Mar;107(3):265-71. Epub 2004 Jan 20.
PMID: 14735304 [PubMed - indexed for MEDLINE]

170: Di Muzio A, Capasso M, Verrotti A, Trotta D, Lupo S, Pappalepore N,
Manzoli C, Chiarelli F, Uncini A.
Macrophagic myofasciitis: an infantile Italian case.
Neuromuscul Disord. 2004 Feb;14(2):175-7.
PMID: 14733966 [PubMed - indexed for MEDLINE]

171: Saito F, Tomimitsu H, Arai K, Nakai S, Kanda T, Shimizu T, Mizusawa H,
Matsumura K.
A Japanese patient with distal myopathy with rimmed vacuoles: missense
mutations in the epimerase domain of the UDP-N-acetylglucosamine
2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation
of skeletal muscle glycoproteins.
Neuromuscul Disord. 2004 Feb;14(2):158-61.
PMID: 14733963 [PubMed - indexed for MEDLINE]

172: Bronner IM, Linssen WH, van der Meulen MF, Hoogendijk JE, de Visser M.
Polymyositis: an ongoing discussion about a disease entity.
Arch Neurol. 2004 Jan;61(1):132-5.
PMID: 14732633 [PubMed - indexed for MEDLINE]

173: Bao YP, Sarkar S, Uyama E, Rubinsztein DC.
Congo red, doxycycline, and HSP70 overexpression reduce aggregate formation and
cell death in cell models of oculopharyngeal muscular dystrophy.
J Med Genet. 2004 Jan;41(1):47-51. No abstract available.
PMID: 14729833 [PubMed - indexed for MEDLINE]

174: Fidzianska A, Rowinska-Marcinska K, Hausmanowa-Petrusewicz I.
Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with
inclusion body myositis-like morphology.
Acta Neuropathol (Berl). 2004 Mar;107(3):197-203. Epub 2004 Jan 8.
PMID: 14712398 [PubMed - indexed for MEDLINE]

175: van der Pas J, Hengstman GJ, ter Laak HJ, Borm GF, van Engelen BG.
Diagnostic value of MHC class I staining in idiopathic inflammatory myopathies.
J Neurol Neurosurg Psychiatry. 2004 Jan;75(1):136-9.
PMID: 14707323 [PubMed - indexed for MEDLINE]

176: Kovacs GG, Lindeck-Pozza E, Chimelli L, Araujo AQ, Gabbai AA, Strobel T,
Glatzel M, Aguzzi A, Budka H.
Creutzfeldt-Jakob disease and inclusion body myositis: abundant
disease-associated prion protein in muscle.
Ann Neurol. 2004 Jan;55(1):121-5.
PMID: 14705121 [PubMed - indexed for MEDLINE]

177: Vattemi G, Engel WK, McFerrin J, Askanas V.
Endoplasmic reticulum stress and unfolded protein response in inclusion body
myositis muscle.
Am J Pathol. 2004 Jan;164(1):1-7.
PMID: 14695312 [PubMed - indexed for MEDLINE]

178: Mankodi A, Teng-Umnuay P, Krym M, Henderson D, Swanson M, Thornton CA.
Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2.
Ann Neurol. 2003 Dec;54(6):760-8.
PMID: 14681885 [PubMed - indexed for MEDLINE]

179: Krause S, Schlotter-Weigel B, Walter MC, Najmabadi H, Wiendl H,
Muller-Hocker J, Muller-Felber W, Pongratz D, Lochmuller H.
A novel homozygous missense mutation in the GNE gene of a patient with
quadriceps-sparing hereditary inclusion body myopathy associated with muscle
inflammation.
Neuromuscul Disord. 2003 Dec;13(10):830-4.
PMID: 14678807 [PubMed - indexed for MEDLINE]

180: Sugaya K, Matsubara S, Miyamoto K, Kawata A, Hayashi H.
An aggregate-prone conformational epitope in trinucleotide repeat diseases.
Neuroreport. 2003 Dec 19;14(18):2331-5.
PMID: 14663186 [PubMed - indexed for MEDLINE]

181: Onengut S, Ugur SA, Karasoy H, Yuceyar N, Tolun A.
Identification of a locus for an autosomal recessive hyaline body myopathy at
chromosome 3p22.2-p21.32.
Neuromuscul Disord. 2004 Jan;14(1):4-9.
PMID: 14659406 [PubMed - indexed for MEDLINE]

182: Lampe JB, Gossrau G, Kempe A, Fussel M, Schwurack K, Schroder R, Krause S,
Kohnen R, Walter MC, Reichmann H, Lochmuller H.
Analysis of HLA class I and II alleles in sporadic inclusion-body myositis.
J Neurol. 2003 Nov;250(11):1313-7.
PMID: 14648147 [PubMed - indexed for MEDLINE]

183: Miller FW, Rider LG, Plotz PH, Isenberg DA, Oddis CV.
Diagnostic criteria for polymyositis and dermatomyositis.
Lancet. 2003 Nov 22;362(9397):1762-3; author reply 1763. No abstract available.
PMID: 14643132 [PubMed - indexed for MEDLINE]

184: Figarella-Branger D, Civatte M, Bartoli C, Pellissier JF.
Cytokines, chemokines, and cell adhesion molecules in inflammatory myopathies.
Muscle Nerve. 2003 Dec;28(6):659-82. Review.
PMID: 14639580 [PubMed - indexed for MEDLINE]

185: Choi YC, Kim TS, Kim SY.
Increase in transglutaminase 2 in idiopathic inflammatory myopathies.
Eur Neurol. 2004;51(1):10-4. Epub 2003 Nov 18.
PMID: 14631123 [PubMed - indexed for MEDLINE]

186: Tateyama M, Saito N, Fujihara K, Shiga Y, Takeda A, Narikawa K, Hasegawa
T, Taguchi Y, Sakuma R, Onodera Y, Ohnuma A, Tobita M, Itoyama Y.
Familial inclusion body myositis: a report on two Japanese sisters.
Intern Med. 2003 Oct;42(10):1035-8.
PMID: 14606722 [PubMed - indexed for MEDLINE]

187: Mizusawa H.
The familial occurrence may give a clue to the pathogenesis of inclusion body
myositis.
Intern Med. 2003 Oct;42(10):928-9. No abstract available.
PMID: 14606702 [PubMed - indexed for MEDLINE]

188: Dalakas MC.
High-dose intravenous immunoglobulin in inflammatory myopathies: experience
based on controlled clinical trials.
Neurol Sci. 2003 Oct;24 Suppl 4:S256-9. Review.
PMID: 14598055 [PubMed - indexed for MEDLINE]

189: Derk CT, Vivino FB, Kenyon L, Mandel S.
Inclusion body myositis in connective tissue disorders: case report and review
of the literature.
Clin Rheumatol. 2003 Oct;22(4-5):324-8. Review.
PMID: 14576992 [PubMed - indexed for MEDLINE]

190: Askanas V, Engel WK.
Proposed pathogenetic cascade of inclusion-body myositis: importance of
amyloid-beta, misfolded proteins, predisposing genes, and aging.
Curr Opin Rheumatol. 2003 Nov;15(6):737-44. Review.
PMID: 14569203 [PubMed - indexed for MEDLINE]

191: Harris-Love MO.
Physical activity and disablement in the idiopathic inflammatory myopathies.
Curr Opin Rheumatol. 2003 Nov;15(6):679-90. Review.
PMID: 14569196 [PubMed - indexed for MEDLINE]

192: Hong Y, Stanley P.
Lec3 Chinese hamster ovary mutants lack UDP-N-acetylglucosamine 2-epimerase
activity because of mutations in the epimerase domain of the Gne gene.
J Biol Chem. 2003 Dec 26;278(52):53045-54. Epub 2003 Oct 15.
PMID: 14561743 [PubMed - indexed for MEDLINE]

193: Kumamoto T, Ueyama H, Tsumura H, Toyoshima I, Tsuda T.
Expression of lysosome-related proteins and genes in the skeletal muscles of
inclusion body myositis.
Acta Neuropathol (Berl). 2004 Jan;107(1):59-65. Epub 2003 Sep 26.
PMID: 14513262 [PubMed - indexed for MEDLINE]

194: Dalakas MC, Hohlfeld R.
Polymyositis and dermatomyositis.
Lancet. 2003 Sep 20;362(9388):971-82. Review.
PMID: 14511932 [PubMed - indexed for MEDLINE]

195: Amato AA, Griggs RC.
Treatment of idiopathic inflammatory myopathies.
Curr Opin Neurol. 2003 Oct;16(5):569-75. Review.
PMID: 14501840 [PubMed - indexed for MEDLINE]

196: Raju R, Vasconcelos O, Granger R, Dalakas MC.
Expression of IFN-gamma-inducible chemokines in inclusion body myositis.
J Neuroimmunol. 2003 Aug;141(1-2):125-31.
PMID: 12965263 [PubMed - indexed for MEDLINE]

197: Fan X, Messaed C, Dion P, Laganiere J, Brais B, Karpati G, Rouleau GA.
HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.
Can J Neurol Sci. 2003 Aug;30(3):244-51.
PMID: 12945950 [PubMed - indexed for MEDLINE]

198: Williams SF, Mincey BA, Calamia KT.
Inclusion body myositis associated with celiac sprue and idiopathic
thrombocytopenic purpura.
South Med J. 2003 Jul;96(7):721-3.
PMID: 12940332 [PubMed - indexed for MEDLINE]

199: Seeliger S, Vogl T, Engels IH, Schroder JM, Sorg C, Sunderkotter C, Roth
J.
Expression of calcium-binding proteins MRP8 and MRP14 in inflammatory muscle
diseases.
Am J Pathol. 2003 Sep;163(3):947-56. Erratum in: Am J Pathol. 2003
Dec;163(6):2645.
PMID: 12937135 [PubMed - indexed for MEDLINE]

200: Wiendl H, Mitsdoerffer M, Schneider D, Chen L, Lochmuller H, Melms A,
Weller M.
Human muscle cells express a B7-related molecule, B7-H1, with strong negative
immune regulatory potential: a novel mechanism of counterbalancing the immune
attack in idiopathic inflammatory myopathies.
FASEB J. 2003 Oct;17(13):1892-4. Epub 2003 Aug 15.
PMID: 12923066 [PubMed - indexed for MEDLINE]

201: Watts GD, Thorne M, Kovach MJ, Pestronk A, Kimonis VE.
Clinical and genetic heterogeneity in chromosome 9p associated hereditary
inclusion body myopathy: exclusion of GNE and three other candidate genes.
Neuromuscul Disord. 2003 Sep;13(7-8):559-67.
PMID: 12921793 [PubMed - indexed for MEDLINE]

202: Hengstman GJ.
Magnetic resonance imaging criteria to differentiate inclusion body myositis
from polymyositis.
J Rheumatol. 2003 Aug;30(8):1892. No abstract available.
PMID: 12913890 [PubMed - indexed for MEDLINE]

203: Nakano S, Shinde A, Ito H, Ito H, Kusaka H.
MAP kinase phosphatase-1 is induced in abnormal fibers in inclusion body
myositis.
Neurology. 2003 Aug 12;61(3):322-6.
PMID: 12913191 [PubMed - indexed for MEDLINE]

204: van der Meulen MF, Bronner IM, Hoogendijk JE, Burger H, van Venrooij WJ,
Voskuyl AE, Dinant HJ, Linssen WH, Wokke JH, de Visser M.
Polymyositis: an overdiagnosed entity.
Neurology. 2003 Aug 12;61(3):316-21.
PMID: 12913190 [PubMed - indexed for MEDLINE]

205: Amato AA, Griggs RC.
Unicorns, dragons, polymyositis, and other mythological beasts.
Neurology. 2003 Aug 12;61(3):288-9. No abstract available.
PMID: 12913184 [PubMed - indexed for MEDLINE]

206: Dalakas MC.
Therapeutic approaches in patients with inflammatory myopathies.
Semin Neurol. 2003 Jun;23(2):199-206. Review.
PMID: 12894385 [PubMed - indexed for MEDLINE]

207: Lindberg C, Trysberg E, Tarkowski A, Oldfors A.
Anti-T-lymphocyte globulin treatment in inclusion body myositis: a randomized
pilot study.
Neurology. 2003 Jul 22;61(2):260-2.
PMID: 12874415 [PubMed - indexed for MEDLINE]

208: Askanas V, Engel WK, McFerrin J, Vattemi G.
Transthyretin Val122Ile, accumulated Abeta, and inclusion-body myositis aspects
in cultured muscle.
Neurology. 2003 Jul 22;61(2):257-60.
PMID: 12874414 [PubMed - indexed for MEDLINE]

209: Selva-O'Callaghan A, Mijares-Boeckh-Behrens T, Labrador-Horrillos M,
Solans-Laque R, Ma Grau-Junyent J, Vilardell-Tarres M.
Anti-PM-Scl antibodies in a patient with inclusion body myositis.
Rheumatology (Oxford). 2003 Aug;42(8):1016-8. Review. No abstract available.
PMID: 12869677 [PubMed - indexed for MEDLINE]

210: Massawi G, Hickling P, Hilton D, Patterson C.
Inclusion body myositis evolving in systemic lupus erythrematosus? A case
report.
Rheumatology (Oxford). 2003 Aug;42(8):1012-4. Review. No abstract available.
PMID: 12869675 [PubMed - indexed for MEDLINE]

211: Muntzing K, Lindberg C, Moslemi AR, Oldfors A.
Inclusion body myositis: clonal expansions of muscle-infiltrating T cells
persist over time.
Scand J Immunol. 2003 Aug;58(2):195-200.
PMID: 12869141 [PubMed - indexed for MEDLINE]

212: Isenberg DA, Allen E, Farewell V, Ehrenstein MR, Hanna MG, Lundberg IE,
Oddis C, Pilkington C, Plotz P, Scott D, Vencovsky J, Cooper R, Rider L, Miller
F; International Myositis and Clinical Studies Group (IMACS).
International consensus outcome measures for patients with idiopathic
inflammatory myopathies. Development and initial validation of myositis activity
and damage indices in patients with adult onset disease.
Rheumatology (Oxford). 2004 Jan;43(1):49-54. Epub 2003 Jul 16. Review.
PMID: 12867580 [PubMed - indexed for MEDLINE]

213: Ito H, Kamei K, Iwamoto I, Inaguma Y, Tsuzuki M, Kishikawa M, Shimada A,
Hosokawa M, Kato K.
Hsp27 suppresses the formation of inclusion bodies induced by expression of
R120G alpha B-crystallin, a cause of desmin-related myopathy.
Cell Mol Life Sci. 2003 Jun;60(6):1217-23.
PMID: 12861387 [PubMed - indexed for MEDLINE]

214: Hinderlich S, Salama I, Eisenberg I, Mitrani-Rosenbaum S.
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body
myopathy.
Neurology. 2003 Jul 8;61(1):145; author reply 145. No abstract available.
PMID: 12847185 [PubMed - indexed for MEDLINE]

215: Loutfy MR, Sheehan NL, Goodhew JE, Walmsley SL.
Inclusion body myositis: another possible manifestation of
antiretroviral-associated mitochondrial toxicity.
AIDS. 2003 May 23;17(8):1266-7. No abstract available.
PMID: 12819534 [PubMed - indexed for MEDLINE]

216: Parissis D, Karkavelas G, Taskos N, Milonas I.
Inclusion body myositis in a patient with a presumed diagnosis of post-polio
syndrome.
J Neurol. 2003 May;250(5):619-21. No abstract available.
PMID: 12814114 [PubMed - indexed for MEDLINE]

217: Del Bo R, Baron P, Prelle A, Serafini M, Moggio M, Fonzo AD, Castagni M,
Bresolin N, Comi GP.
Novel missense mutation and large deletion of GNE gene in autosomal-recessive
inclusion-body myopathy.
Muscle Nerve. 2003 Jul;28(1):113-7.
PMID: 12811782 [PubMed - indexed for MEDLINE]

218: Arnardottir S, Svanborg E, Borg K.
Inclusion body myositis--sensory dysfunction revealed with quantitative
determination of somatosensory thresholds.
Acta Neurol Scand. 2003 Jul;108(1):22-7.
PMID: 12807389 [PubMed - indexed for MEDLINE]

219: Vattemi G, Engel WK, McFerrin J, Askanas V.
Cystatin C colocalizes with amyloid-beta and coimmunoprecipitates with
amyloid-beta precursor protein in sporadic inclusion-body myositis muscles.
J Neurochem. 2003 Jun;85(6):1539-46.
PMID: 12787072 [PubMed - indexed for MEDLINE]

220: Weeks DA, Nixon RR, Kaimaktchiev V, Mierau GW.
Intranuclear rod myopathy, a rare and morphologically striking variant of
nemaline rod myopathy.
Ultrastruct Pathol. 2003 May-Jun;27(3):151-4.
PMID: 12775505 [PubMed - indexed for MEDLINE]

221: Argov Z, Eisenberg I, Grabov-Nardini G, Sadeh M, Wirguin I, Soffer D,
Mitrani-Rosenbaum S.
Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.
Neurology. 2003 May 13;60(9):1519-23.
PMID: 12743242 [PubMed - indexed for MEDLINE]

222: Martin PT, Freeze HH.
Glycobiology of neuromuscular disorders.
Glycobiology. 2003 Aug;13(8):67R-75R. Epub 2003 May 7. Review.
PMID: 12736200 [PubMed - indexed for MEDLINE]

223: Askanas V, Engel WK.
Unfolding story of inclusion-body myositis and myopathies: role of misfolded
proteins, amyloid-beta, cholesterol, and aging.
J Child Neurol. 2003 Mar;18(3):185-90.
PMID: 12731644 [PubMed - indexed for MEDLINE]

224: Fidzianska A, Kaminska A.
Congenital myopathy with abundant ring fibres, rimmed vacuoles and inclusion
body myositis-type inclusions.
Neuropediatrics. 2003 Feb;34(1):40-4.
PMID: 12690567 [PubMed - indexed for MEDLINE]

225: Wiendl H, Mitsdoerffer M, Schneider D, Melms A, Lochmuller H, Hohlfeld R,
Weller M.
Muscle fibres and cultured muscle cells express the B7.1/2-related inducible
co-stimulatory molecule, ICOSL: implications for the pathogenesis of
inflammatory myopathies.
Brain. 2003 May;126(Pt 5):1026-35.
PMID: 12690043 [PubMed - indexed for MEDLINE]

226: Hewitt JE, Grewal PK.
Glycosylation defects in inherited muscle disease.
Cell Mol Life Sci. 2003 Feb;60(2):251-8. Review.
PMID: 12678490 [PubMed - indexed for MEDLINE]

227: Olive M, Goldfarb L, Dagvadorj A, Sambuughin N, Paulin D, Li Z, Goudeau B,
Vicart P, Ferrer I.
Expression of the intermediate filament protein synemin in myofibrillar
myopathies and other muscle diseases.
Acta Neuropathol (Berl). 2003 Jul;106(1):1-7. Epub 2003 Apr 1.
PMID: 12669240 [PubMed - indexed for MEDLINE]

228: Mastaglia FL, Garlepp MJ, Phillips BA, Zilko PJ.
Inflammatory myopathies: clinical, diagnostic and therapeutic aspects.
Muscle Nerve. 2003 Apr;27(4):407-25. Review.
PMID: 12661042 [PubMed - indexed for MEDLINE]

229: Monici MC, Aguennouz M, Mazzeo A, Messina C, Vita G.
Activation of nuclear factor-kappaB in inflammatory myopathies and Duchenne
muscular dystrophy.
Neurology. 2003 Mar 25;60(6):993-7.
PMID: 12654966 [PubMed - indexed for MEDLINE]

230: Fan X, Rouleau GA.
Progress in understanding the pathogenesis of oculopharyngeal muscular
dystrophy.
Can J Neurol Sci. 2003 Feb;30(1):8-14. Review.
PMID: 12619777 [PubMed - indexed for MEDLINE]

231: Vattemi G, Engel WK, McFerrin J, Pastorino L, Buxbaum JD, Askanas V.
BACE1 and BACE2 in pathologic and normal human muscle.
Exp Neurol. 2003 Feb;179(2):150-8.
PMID: 12618121 [PubMed - indexed for MEDLINE]

232: Arnardottir S, Alexanderson H, Lundberg IE, Borg K.
Sporadic inclusion body myositis: pilot study on the effects of a home exercise
program on muscle function, histopathology and inflammatory reaction.
J Rehabil Med. 2003 Jan;35(1):31-5.
PMID: 12610846 [PubMed - indexed for MEDLINE]

233: Suwa K, Mizuguchi M, Momoi MY, Nakamura M, Arima K, Komaki H, Nonaka I.
Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with
nemaline myopathy.
Neuropathology. 2002 Dec;22(4):294-8.
PMID: 12564770 [PubMed - indexed for MEDLINE]

234: Mastaglia FL, Phillips BA.
Idiopathic inflammatory myopathies: epidemiology, classification, and
diagnostic criteria.
Rheum Dis Clin North Am. 2002 Nov;28(4):723-41. Review.
PMID: 12510664 [PubMed - indexed for MEDLINE]

235: Yazici Y, Kagen LJ.
Clinical presentation of the idiopathic inflammatory myopathies.
Rheum Dis Clin North Am. 2002 Nov;28(4):823-32. Review.
PMID: 12506774 [PubMed - indexed for MEDLINE]

236: Dalakas MC.
Muscle biopsy findings in inflammatory myopathies.
Rheum Dis Clin North Am. 2002 Nov;28(4):779-98, vi. Review.
PMID: 12506772 [PubMed - indexed for MEDLINE]

237: Eisenberg I, Grabov-Nardini G, Hochner H, Korner M, Sadeh M, Bertorini T,
Bushby K, Castellan C, Felice K, Mendell J, Merlini L, Shilling C, Wirguin I,
Argov Z, Mitrani-Rosenbaum S.
Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the
quadriceps.
Hum Mutat. 2003 Jan;21(1):99.
PMID: 12497639 [PubMed - indexed for MEDLINE]

238: Broccolini A, Pescatori M, D'Amico A, Sabino A, Silvestri G, Ricci E,
Servidei S, Tonali PA, Mirabella M.
An Italian family with autosomal recessive inclusion-body myopathy and
mutations in the GNE gene.
Neurology. 2002 Dec 10;59(11):1808-9. No abstract available.
PMID: 12473780 [PubMed - indexed for MEDLINE]

239: Vasconcelos OM, Raju R, Dalakas MC.
GNE mutations in an American family with quadriceps-sparing IBM and lack of
mutations in s-IBM.
Neurology. 2002 Dec 10;59(11):1776-9.
PMID: 12473769 [PubMed - indexed for MEDLINE]

240: Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida
K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M,
Aoki M, Nonaka I.
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body
myopathy.
Neurology. 2002 Dec 10;59(11):1689-93.
PMID: 12473753 [PubMed - indexed for MEDLINE]

241: Dorph C, Lundberg IE.
Idiopathic inflammatory myopathies - myositis.
Best Pract Res Clin Rheumatol. 2002 Dec;16(5):817-32. Review.
PMID: 12473276 [PubMed - indexed for MEDLINE]

242: Mastaglia FL, Zilko PJ.
Inflammatory myopathies: how to treat the difficult cases.
J Clin Neurosci. 2003 Jan;10(1):99-101. Review.
PMID: 12464534 [PubMed - indexed for MEDLINE]

243: Darvish D.
Magnesium may help patients with recessive hereditary inclusion body myopathy,
a pathological review.
Med Hypotheses. 2003 Jan;60(1):94-101. Review.
PMID: 12450772 [PubMed - indexed for MEDLINE]

244: van der Meulen MF, van Wichen DF, van Blokland WT, van den Berg LH, Wokke
JH, Hoogendijk JE, de Weger RA.
Evidence for heterogeneity of T cell expansion in polymyositis and inclusion
body myositis.
J Neuroimmunol. 2002 Dec;133(1-2):198-204.
PMID: 12446023 [PubMed - indexed for MEDLINE]

245: Kumada S, Uchihara T, Hayashi M, Nakamura A, Kikuchi E, Mizutani T, Oda M.

Promyelocytic leukemia protein is redistributed during the formation of
intranuclear inclusions independent of polyglutamine expansion: an
immunohistochemical study on Marinesco bodies.
J Neuropathol Exp Neurol. 2002 Nov;61(11):984-91.
PMID: 12430715 [PubMed - indexed for MEDLINE]

246: Raymond JT, Reichard T, Shellabarger W, Nordhausen R, Garner MM.
Inclusion body myositis in spring peepers (Pseudacris crucifer).
J Vet Diagn Invest. 2002 Nov;14(6):501-3.
PMID: 12423034 [PubMed - indexed for MEDLINE]

247: Tawil R, Griggs RC.
Inclusion body myositis.
Curr Opin Rheumatol. 2002 Nov;14(6):653-7. Review.
PMID: 12410086 [PubMed - indexed for MEDLINE]

248: Darvish D, Vahedifar P, Huo Y.
Four novel mutations associated with autosomal recessive inclusion body
myopathy (MIM: 600737).
Mol Genet Metab. 2002 Nov;77(3):252-6.
PMID: 12409274 [PubMed - indexed for MEDLINE]

249: Dalakas MC.
Understanding the immunopathogenesis of inclusion-body myositis: present and
future prospects.
Rev Neurol (Paris). 2002 Oct;158(10 Pt 1):948-58. Review.
PMID: 12407303 [PubMed - indexed for MEDLINE]

250: Dahlbom K, Lindberg C, Oldfors A.
Inclusion body myositis: morphological clues to correct diagnosis.
Neuromuscul Disord. 2002 Nov;12(9):853-7.
PMID: 12398837 [PubMed - indexed for MEDLINE]

251: Chan HY, Warrick JM, Andriola I, Merry D, Bonini NM.
Genetic modulation of polyglutamine toxicity by protein conjugation pathways in
Drosophila.
Hum Mol Genet. 2002 Nov 1;11(23):2895-904.
PMID: 12393801 [PubMed - indexed for MEDLINE]

252: Greenberg SA, Sanoudou D, Haslett JN, Kohane IS, Kunkel LM, Beggs AH,
Amato AA.
Molecular profiles of inflammatory myopathies.
Neurology. 2002 Oct 22;59(8):1170-82.
PMID: 12391344 [PubMed - indexed for MEDLINE]

253: Wanschit J, Nakano S, Goudeau B, Strobel T, Rinner W, Wimmer G, Resch H,
Jaksch M, Akiguchi I, Vicart P, Budka H.
Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3
cases and review of the literature.
Clin Neuropathol. 2002 Sep-Oct;21(5):220-31. Review.
PMID: 12365725 [PubMed - indexed for MEDLINE]

254: Taratuto AL.
Congenital myopathies and related disorders.
Curr Opin Neurol. 2002 Oct;15(5):553-61. Review.
PMID: 12351999 [PubMed - indexed for MEDLINE]

255: Askanas V, Engel WK.
Inclusion-body myositis and myopathies: different etiologies, possibly similar
pathogenic mechanisms.
Curr Opin Neurol. 2002 Oct;15(5):525-31. Review.
PMID: 12351995 [PubMed - indexed for MEDLINE]

256: Arai A, Tanaka K, Ikeuchi T, Igarashi S, Kobayashi H, Asaka T, Date H,
Saito M, Tanaka H, Kawasaki S, Uyama E, Mizusawa H, Fukuhara N, Tsuji S.
A novel mutation in the GNE gene and a linkage disequilibrium in Japanese
pedigrees.
Ann Neurol. 2002 Oct;52(4):516-9.
PMID: 12325084 [PubMed - indexed for MEDLINE]

257: Dion E, Cherin P, Payan C, Fournet JC, Papo T, Maisonobe T, Auberton E,
Chosidow O, Godeau P, Piette JC, Herson S, Grenier P.
Magnetic resonance imaging criteria for distinguishing between inclusion body
myositis and polymyositis.
J Rheumatol. 2002 Sep;29(9):1897-906.
PMID: 12233884 [PubMed - indexed for MEDLINE]

258: Askanas V, Engel WK.
Newest pathogenetic considerations in inclusion-body myositis: possible role of
amyloid-beta, cholesterol, relation to aging and to Alzheimer's disease.
Curr Rheumatol Rep. 2002 Oct;4(5):427-33. Review.
PMID: 12217248 [PubMed - indexed for MEDLINE]

259: Buchbinder R, Hill CL.
Malignancy in patients with inflammatory myopathy.
Curr Rheumatol Rep. 2002 Oct;4(5):415-26. Review.
PMID: 12217247 [PubMed - indexed for MEDLINE]

260: Tomimitsu H, Ishikawa K, Shimizu J, Ohkoshi N, Kanazawa I, Mizusawa H.
Distal myopathy with rimmed vacuoles: novel mutations in the GNE gene.
Neurology. 2002 Aug 13;59(3):451-4.
PMID: 12177386 [PubMed - indexed for MEDLINE]

261: Fischer D, Matten J, Reimann J, Bonnemann C, Schroder R.
Expression, localization and functional divergence of alphaB-crystallin and
heat shock protein 27 in core myopathies and neurogenic atrophy.
Acta Neuropathol (Berl). 2002 Sep;104(3):297-304. Epub 2002 Jun 8.
PMID: 12172916 [PubMed - indexed for MEDLINE]

262: Tsuchiya K, Ikeda K, Mimura M, Takahashi M, Miyazaki H, Anno M, Shiotsu H,
Akabane H, Niizato K, Uchihara T, Tominaga I, Nakano I.
Constant involvement of the Betz cells and pyramidal tract in amyotrophic
lateral sclerosis with dementia: a clinicopathological study of eight autopsy
cases.
Acta Neuropathol (Berl). 2002 Sep;104(3):249-59. Epub 2002 Jul 4.
PMID: 12172910 [PubMed - indexed for MEDLINE]

263: Kissel JT.
Misunderstandings, misperceptions, and mistakes in the management of the
inflammatory myopathies.
Semin Neurol. 2002 Mar;22(1):41-51. Review.
PMID: 12170392 [PubMed - indexed for MEDLINE]

264: Rosso SM, van Swieten JC.
New developments in frontotemporal dementia and parkinsonism linked to
chromosome 17.
Curr Opin Neurol. 2002 Aug;15(4):423-8. Review.
PMID: 12151838 [PubMed - indexed for MEDLINE]

265: Goebel HH, Borchert A.
Protein surplus myopathies and other rare congenital myopathies.
Semin Pediatr Neurol. 2002 Jun;9(2):160-70. Review.
PMID: 12139000 [PubMed - indexed for MEDLINE]

266: Eisenberg I, Barash M, Kahan T, Mitrani-Rosenbaum S.
Cloning and characterization of a human novel gene C9orf19 encoding a conserved
putative protein with an SCP-like extracellular protein domain.
Gene. 2002 Jun 26;293(1-2):141-8.
PMID: 12137952 [PubMed - indexed for MEDLINE]

267: De Bleecker JL, De Paepe B, Vanwalleghem IE, Schroder JM.
Differential expression of chemokines in inflammatory myopathies.
Neurology. 2002 Jun 25;58(12):1779-85.
PMID: 12084877 [PubMed - indexed for MEDLINE]

268: Vital C, Bouillot S, Canron MH, Vital A.
Schwannian crystalline-like inclusions bodies (Fardeau-Engel bodies) revisited
in peripheral neuropathies.
Ultrastruct Pathol. 2002 Jan-Feb;26(1):9-13.
PMID: 12028653 [PubMed - indexed for MEDLINE]

269: Fyhr IM, Lindberg C, Oldfors A.
Expression of Bcl-2 in inclusion body myositis.
Acta Neurol Scand. 2002 May;105(5):403-7.
PMID: 11982494 [PubMed - indexed for MEDLINE]

270: Sugarman MC, Yamasaki TR, Oddo S, Echegoyen JC, Murphy MP, Golde TE,
Jannatipour M, Leissring MA, LaFerla FM.
Inclusion body myositis-like phenotype induced by transgenic overexpression of
beta APP in skeletal muscle.
Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6334-9. Epub 2002 Apr 23.
PMID: 11972038 [PubMed - indexed for MEDLINE]

271: Littleton ET, Man WD, Holton JL, Landon DN, Hanna MG, Polkey MI, Taylor
GP.
Human T cell leukaemia virus type I associated neuromuscular disease causing
respiratory failure.
J Neurol Neurosurg Psychiatry. 2002 May;72(5):650-2.
PMID: 11971056 [PubMed - indexed for MEDLINE]

272: Kanellopoulos P, Baltoyiannis C, Tzioufas AG.
Primary Sjogren's syndrome associated with inclusion body myositis.
Rheumatology (Oxford). 2002 Apr;41(4):440-4.
PMID: 11961175 [PubMed - indexed for MEDLINE]

273: Hilton DA, McLean B.
December 2001: rapidly progressive motor weakness, starting in pregnancy.
Brain Pathol. 2002 Apr;12(2):267-8, 269.
PMID: 11958383 [PubMed - indexed for MEDLINE]

274: Hengstman GJ, Brouwer R, Egberts WT, Seelig HP, Jongen PJ, van Venrooij
WJ, van Engelen BG.
Clinical and serological characteristics of 125 Dutch myositis patients.
Myositis specific autoantibodies aid in the differential diagnosis of the
idiopathic inflammatory myopathies.
J Neurol. 2002 Jan;249(1):69-75.
PMID: 11954871 [PubMed - indexed for MEDLINE]

275: Lindvall B, Bengtsson A, Ernerudh J, Eriksson P.
Subclinical myositis is common in primary Sjogren's syndrome and is not related
to muscle pain.
J Rheumatol. 2002 Apr;29(4):717-25.
PMID: 11950012 [PubMed - indexed for MEDLINE]

276: Rutkove SB, Parker RA, Nardin RA, Connolly CE, Felice KJ, Raynor EM.
A pilot randomized trial of oxandrolone in inclusion body myositis.
Neurology. 2002 Apr 9;58(7):1081-7.
PMID: 11940697 [PubMed - indexed for MEDLINE]

277: Schoser BG, Blottner D, Stuerenburg HJ.
Matrix metalloproteinases in inflammatory myopathies: enhanced immunoreactivity
near atrophic myofibers.
Acta Neurol Scand. 2002 Apr;105(4):309-13.
PMID: 11939944 [PubMed - indexed for MEDLINE]

278: Lewandowska E, Schmidt-Sidor B, Mierzewska H, Pasennik E, Kohutnicka M.
Ultrastructural study of mother and daughter muscle changes with mitochondrial
encephalomyopathy.
Folia Neuropathol. 2001;39(4):271-6.
PMID: 11928899 [PubMed - indexed for MEDLINE]

279: Kayashima T, Matsuo H, Satoh A, Ohta T, Yoshiura K, Matsumoto N, Nakane Y,
Niikawa N, Kishino T.
Nonaka myopathy is caused by mutations in the
UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE).
J Hum Genet. 2002;47(2):77-9.
PMID: 11916006 [PubMed - indexed for MEDLINE]

280: Lacson AG, D'Cruz CA, Gilbert-Barness E, Sharer L, Jacinto S, Cuenca R.
Aluminum phagocytosis in quadriceps muscle following vaccination in children:
relationship to macrophagic myofasciitis.
Pediatr Dev Pathol. 2002 Mar-Apr;5(2):151-8.
PMID: 11910509 [PubMed - indexed for MEDLINE]

281: Badrising UA, Maat-Schieman ML, Ferrari MD, Zwinderman AH, Wessels JA,
Breedveld FC, van Doorn PA, van Engelen BG, Hoogendijk JE, Howeler CJ, de Jager
AE, Jennekens FG, Koehler PJ, de Visser M, Viddeleer A, Verschuuren JJ, Wintzen
AR.
Comparison of weakness progression in inclusion body myositis during treatment
with methotrexate or placebo.
Ann Neurol. 2002 Mar;51(3):369-72.
PMID: 11891832 [PubMed - indexed for MEDLINE]

282: Waggoner B, Kovach MJ, Winkelman M, Cai D, Khardori R, Gelber D, Kimonis
VE.
Heterogeneity in familial dominant Paget disease of bone and muscular
dystrophy.
Am J Med Genet. 2002 Mar 15;108(3):187-91.
PMID: 11891683 [PubMed - indexed for MEDLINE]

283: Tajsharghi H, Thornell LE, Darin N, Martinsson T, Kyllerman M, Wahlstrom
J, Oldfors A.
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression
increases with age.
Neurology. 2002 Mar 12;58(5):780-6.
PMID: 11889243 [PubMed - indexed for MEDLINE]

284: Rutkove SB, Aaron R, Shiffman CA.
Localized bioimpedance analysis in the evaluation of neuromuscular disease.
Muscle Nerve. 2002 Mar;25(3):390-7.
PMID: 11870716 [PubMed - indexed for MEDLINE]

285: Jaworska-Wilczynska M, Wilczynski GM, Engel WK, Strickland DK, Weisgraber
KH, Askanas V.
Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle.
Neurology. 2002 Feb 12;58(3):438-45.
PMID: 11839845 [PubMed - indexed for MEDLINE]

286: Tsuruta Y, Furuta A, Taniguchi N, Yamada T, Kira J, Iwaki T.
Increased expression of manganese superoxide dismutase is associated with that
of nitrotyrosine in myopathies with rimmed vacuoles.
Acta Neuropathol (Berl). 2002 Jan;103(1):59-65.
PMID: 11837748 [PubMed - indexed for MEDLINE]

287: Chen YD, Chen CH, Mak SC, Chi CS.
Stiff-Baby--an unusual manifestation of cytoplasmic body myopathy: report of
one case.
Acta Paediatr Taiwan. 2001 Nov-Dec;42(6):367-9.
PMID: 11811228 [PubMed - indexed for MEDLINE]

288: Cherin P, Pelletier S, Teixeira A, Laforet P, Simon A, Herson S, Eymard B.

Intravenous immunoglobulin for dysphagia of inclusion body myositis.
Neurology. 2002 Jan 22;58(2):326. No abstract available.
PMID: 11805271 [PubMed - indexed for MEDLINE]

289: Ciliberti EF, Prayson RA.
Pathologic quiz case: male with chronic progressive painless muscle weakness.
Arch Pathol Lab Med. 2002 Jan;126(1):105-6. No abstract available.
PMID: 11800662 [PubMed - indexed for MEDLINE]

290: Reddy H, Bendahan D, Lee MA, Johansen-Berg H, Donaghy M, Hilton-Jones D,
Matthews PM.
An expanded cortical representation for hand movement after peripheral motor
denervation.
J Neurol Neurosurg Psychiatry. 2002 Feb;72(2):203-10.
PMID: 11796770 [PubMed - indexed for MEDLINE]

291: Sultan SM, Ioannou Y, Moss K, Isenberg DA.
Outcome in patients with idiopathic inflammatory myositis: morbidity and
mortality.
Rheumatology (Oxford). 2002 Jan;41(1):22-6.
PMID: 11792875 [PubMed - indexed for MEDLINE]

292: Tsuruta Y, Yamada T, Yoshimura T, Satake M, Ogata K, Yamamoto T, Furuya H,
Kira J.
Inclusion body myositis associated with hepatitis C virus infection.
Fukuoka Igaku Zasshi. 2001 Nov;92(11):370-6.
PMID: 11774706 [PubMed - indexed for MEDLINE]

293: Fam AG.
Recent advances in the management of adult myositis.
Expert Opin Investig Drugs. 2001 Jul;10(7):1265-77. Review.
PMID: 11772250 [PubMed - indexed for MEDLINE]

294: Kovach MJ, Waggoner B, Leal SM, Gelber D, Khardori R, Levenstien MA,
Shanks CA, Gregg G, Al-Lozi MT, Miller T, Rakowicz W, Lopate G, Florence J,
Glosser G, Simmons Z, Morris JC, Whyte MP, Pestronk A, Kimonis VE.
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique
dominant disorder in four families: hereditary inclusion body myopathy, Paget
disease of bone, and frontotemporal dementia.
Mol Genet Metab. 2001 Dec;74(4):458-75.
PMID: 11749051 [PubMed - indexed for MEDLINE]

295: Stangel M, Mix E, Zettl UK, Gold R.
Oxides and apoptosis in inflammatory myopathies.
Microsc Res Tech. 2001 Nov 15;55(4):249-58. Review.
PMID: 11748863 [PubMed - indexed for MEDLINE]

296: Vattemi G, Engel WK, McFerrin J, Buxbaum JD, Pastorino L, Askanas V.
Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic
inclusion-body myositis.
Lancet. 2001 Dec 8;358(9297):1962-4.
PMID: 11747923 [PubMed - indexed for MEDLINE]

297: Phillips BA, Cala LA, Thickbroom GW, Melsom A, Zilko PJ, Mastaglia FL.
Patterns of muscle involvement in inclusion body myositis: clinical and
magnetic resonance imaging study.
Muscle Nerve. 2001 Nov;24(11):1526-34.
PMID: 11745956 [PubMed - indexed for MEDLINE]

298: Kim SY, Jeitner TM, Steinert PM.
Transglutaminases in disease.
Neurochem Int. 2002 Jan;40(1):85-103. Review.
PMID: 11738475 [PubMed - indexed for MEDLINE]

299: Wenzel J, Uerlich M, Gerdsen R, Bieber T, Boehm I.
Association of inclusion body myositis with subacute cutaneous lupus
erythematosus.
Rheumatol Int. 2001 Oct;21(2):75-7. Review.
PMID: 11732863 [PubMed - indexed for MEDLINE]

300: Bachmann G, Streppel M, Krug B, Neuen-Jacob E.
Cricopharyngeal muscle hypertrophy associated with florid myositis.
Dysphagia. 2001 Fall;16(4):244-8. Review.
PMID: 11720399 [PubMed - indexed for MEDLINE]

301: Dalakas MC.
The molecular and cellular pathology of inflammatory muscle diseases.
Curr Opin Pharmacol. 2001 Jun;1(3):300-6. Review.
PMID: 11712755 [PubMed - indexed for MEDLINE]

302: Muscle Study Group.
Randomized pilot trial of betaINF1a (Avonex) in patients with inclusion body
myositis.
Neurology. 2001 Nov 13;57(9):1566-70. Erratum in: Neurology 2002 Jan
22;58(2):334.
PMID: 11706093 [PubMed - indexed for MEDLINE]

303: Baron P, Galimberti D, Meda L, Scarpini E, Conti G, Cogiamanian F,
Scarlato G.
Production of IL-6 by human myoblasts stimulated with Abeta: relevance in the
pathogenesis of IBM.
Neurology. 2001 Nov 13;57(9):1561-5.
PMID: 11706091 [PubMed - indexed for MEDLINE]

304: Oldfors A, Fyhr IM.
Inclusion body myositis: genetic factors, aberrant protein expression, and
autoimmunity.
Curr Opin Rheumatol. 2001 Nov;13(6):469-75. Review.
PMID: 11698722 [PubMed - indexed for MEDLINE]

305: Bartoli C, Civatte M, Pellissier JF, Figarella-Branger D.
CCR2A and CCR2B, the two isoforms of the monocyte chemoattractant protein-1
receptor are up-regulated and expressed by different cell subsets in idiopathic
inflammatory myopathies.
Acta Neuropathol (Berl). 2001 Oct;102(4):385-92.
PMID: 11603815 [PubMed - indexed for MEDLINE]

306: Kase S, Shiota G, Fujii Y, Okamoto K, Oyama K, Nakano T, Nomura T, Suou T,
Nakashima K, Ito H, Kawasaki H.
Inclusion body myositis associated with hepatitis C virus infection.
Liver. 2001 Oct;21(5):357-60.
PMID: 11589773 [PubMed - indexed for MEDLINE]

307: Mori S, Hamada H, Yokoyama A, Kohno N, Kondo K, Hara Y, Kawata H, Hiwada
K.
Severe inclusion body myositis with interstitial pneumonia.
Intern Med. 2001 Sep;40(9):940-4.
PMID: 11579961 [PubMed - indexed for MEDLINE]

308: Goebel HH, Halbig LE, Goldfarb L, Schober R, Albani M, Neuen-Jacob E, Voit
T.
Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: a
mixed congenital myopathy.
Neuropediatrics. 2001 Aug;32(4):196-205. Review.
PMID: 11571700 [PubMed - indexed for MEDLINE]

309: Prayson RA, Yu AC.
Bcl-2, Bcl-x, and Bax expression by immunohistochemistry in inclusion body
myositis: a study of 27 cases.
Arch Pathol Lab Med. 2001 Oct;125(10):1326-30.
PMID: 11570908 [PubMed - indexed for MEDLINE]

310: Hilton-Jones D.
Inflammatory muscle diseases.
Curr Opin Neurol. 2001 Oct;14(5):591-6. Review.
PMID: 11562570 [PubMed - indexed for MEDLINE]

311: Felice KJ, North WA.
Inclusion body myositis in Connecticut: observations in 35 patients during an
8-year period.
Medicine (Baltimore). 2001 Sep;80(5):320-7. No abstract available.
PMID: 11552086 [PubMed - indexed for MEDLINE]

312: Eisenberg I, Avidan N, Potikha T, Hochner H, Chen M, Olender T, Barash M,
Shemesh M, Sadeh M, Grabov-Nardini G, Shmilevich I, Friedmann A, Karpati G,
Bradley WG, Baumbach L, Lancet D, Asher EB, Beckmann JS, Argov Z,
Mitrani-Rosenbaum S.
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is
mutated in recessive hereditary inclusion body myopathy.
Nat Genet. 2001 Sep;29(1):83-7.
PMID: 11528398 [PubMed - indexed for MEDLINE]

313: Dabby R, Lange DJ, Trojaborg W, Hays AP, Lovelace RE, Brannagan TH,
Rowland LP.
Inclusion body myositis mimicking motor neuron disease.
Arch Neurol. 2001 Aug;58(8):1253-6.
PMID: 11493165 [PubMed - indexed for MEDLINE]

314: Stojkovic T, Maurage CA, Moerman A, Hurtevent JF, Krivosic-Horber R,
Pellissier JF, Vermersch P.
Congenital myopathy with central cores and fingerprint bodies in association
with malignant hyperthermia susceptibility.
Neuromuscul Disord. 2001 Sep;11(6-7):538-41.
PMID: 11525882 [PubMed - indexed for MEDLINE]

315: Gherardi RK, Coquet M, Cherin P, Belec L, Moretto P, Dreyfus PA,
Pellissier JF, Chariot P, Authier FJ.
Macrophagic myofasciitis lesions assess long-term persistence of
vaccine-derived aluminium hydroxide in muscle.
Brain. 2001 Sep;124(Pt 9):1821-31.
PMID: 11522584 [PubMed - indexed for MEDLINE]

316: Tsuruta Y, Furuta A, Furuta K, Yamada T, Kira J, Iwaki T.
Expression of the lysosome-associated membrane proteins in myopathies with
rimmed vacuoles.
Acta Neuropathol (Berl). 2001 Jun;101(6):579-84.
PMID: 11515786 [PubMed - indexed for MEDLINE]

317: De Bleecker JL, Meire VI, Van Walleghem IE, Groessens IM, Schroder JM.
Immunolocalization of FAS and FAS ligand in inflammatory myopathies.
Acta Neuropathol (Berl). 2001 Jun;101(6):572-8.
PMID: 11515785 [PubMed - indexed for MEDLINE]

318: Rose MR, McDermott MP, Thornton CA, Palenski C, Martens WB, Griggs RC.
A prospective natural history study of inclusion body myositis: implications
for clinical trials.
Neurology. 2001 Aug 14;57(3):548-50.
PMID: 11502935 [PubMed - indexed for MEDLINE]

319: Park JH, Olsen NJ.
Utility of magnetic resonance imaging in the evaluation of patients with
inflammatory myopathies.
Curr Rheumatol Rep. 2001 Aug;3(4):334-45. Review.
PMID: 11470053 [PubMed - indexed for MEDLINE]

320: Lawson Mahowald M.
The benefits and limitations of a physical training program in patients with
inflammatory myositis.
Curr Rheumatol Rep. 2001 Aug;3(4):317-24. Review.
PMID: 11470051 [PubMed - indexed for MEDLINE]

321: Lampe J, Gossrau G, Reichmann H, Walter MC, Mendel B, Lochmuller H.
Prion codon 129 homozygosity and sporadic inclusion body myositis.
Neurology. 2001 Jul 24;57(2):368. No abstract available.
PMID: 11468340 [PubMed - indexed for MEDLINE]

322: Eisenberg I, Hochner H, Shemesh M, Levi T, Potikha T, Sadeh M, Argov Z,
Jackson CL, Mitrani-Rosenbaum S.
Physical and transcriptional map of the hereditary inclusion body myopathy
locus on chromosome 9p12-p13.
Eur J Hum Genet. 2001 Jul;9(7):501-9.
PMID: 11464241 [PubMed - indexed for MEDLINE]

323: Vu TH, Hays AP, Tanji K, Younger D, Gundersen GG, Eastwood A, Braun CW,
DiMauro S, Bonilla E.
Myopathy with tubulin-reactive crystalline inclusions.
Neurology. 2001 Jul 10;57(1):149-52.
PMID: 11445649 [PubMed - indexed for MEDLINE]

324: Wilczynski GM, Engel WK, Askanas V.
Novel cytoplasmic immunolocalization of RNA polymerase II in inclusion-body
myositis muscle.
Neuroreport. 2001 Jul 3;12(9):1809-14.
PMID: 11435903 [PubMed - indexed for MEDLINE]

325: Mukunda BN, Dileep Kumar P, Smith HR.
Long-lasting effectiveness of intravenous immunoglobulin in a patient with
inclusion-body myositis.
Ann Intern Med. 2001 Jun 19;134(12):1156. No abstract available.
PMID: 11412071 [PubMed - indexed for MEDLINE]

326: Buchbinder R, Forbes A, Hall S, Dennett X, Giles G.
Incidence of malignant disease in biopsy-proven inflammatory myopathy. A
population-based cohort study.
Ann Intern Med. 2001 Jun 19;134(12):1087-95.
PMID: 11412048 [PubMed - indexed for MEDLINE]

327: Yamada T, Minohara M, Imaiso Y, Sakae N, Hara H, Tanaka K, Yamamoto T,
Taniwaki T, Furuya H, Kira J.
High-dose vitamin C therapy for inclusion body myositis.
Fukuoka Igaku Zasshi. 2001 Apr;92(4):99-104.
PMID: 11411094 [PubMed - indexed for MEDLINE]

328: Cherin P, Menard D, Mouton P, Viallard JF, Le Hello C, Authier FJ,
Gherardi RK, Coquet M, Herson S, Leroi JP.
Macrophagic myofasciitis associated with inclusion body myositis: a report of
three cases.
Neuromuscul Disord. 2001 Jul;11(5):452-7.
PMID: 11404116 [PubMed - indexed for MEDLINE]

329: van der Meulen MF, Hoogendijk JE, Moons KG, Veldman H, Badrising UA, Wokke
JH.
Rimmed vacuoles and the added value of SMI-31 staining in diagnosing sporadic
inclusion body myositis.
Neuromuscul Disord. 2001 Jul;11(5):447-51.
PMID: 11404115 [PubMed - indexed for MEDLINE]

330: Lampe JB, Walter MC, Reichmann H.
Neurodegeneration-associated proteins and inflammation in sporadic
inclusion-body myositis.
Adv Exp Med Biol. 2001;487:219-28. No abstract available.
PMID: 11403162 [PubMed - indexed for MEDLINE]

331: Querfurth HW, Suhara T, Rosen KM, McPhie DL, Fujio Y, Tejada G, Neve RL,
Adelman LS, Walsh K.
Beta-amyloid peptide expression is sufficient for myotube death: implications
for human inclusion body myopathy.
Mol Cell Neurosci. 2001 May;17(5):793-810.
PMID: 11358479 [PubMed - indexed for MEDLINE]

332: Hengstman GJ, Ter Laak HJ, van Engelen BG, van Venrooij BG.
Anti-Jo-1 positive inclusion body myositis with a marked and sustained clinical
improvement after oral prednisone.
J Neurol Neurosurg Psychiatry. 2001 May;70(5):706. No abstract available.
PMID: 11336039 [PubMed - indexed for MEDLINE]

333: Adachi H, Kume A, Li M, Nakagomi Y, Niwa H, Do J, Sang C, Kobayashi Y,
Doyu M, Sobue G.
Transgenic mice with an expanded CAG repeat controlled by the human AR promoter
show polyglutamine nuclear inclusions and neuronal dysfunction without neuronal
cell death.
Hum Mol Genet. 2001 May 1;10(10):1039-48.
PMID: 11331614 [PubMed - indexed for MEDLINE]

334: Mowzoon N, Sussman A, Bradley WG.
Mycophenolate (CellCept) treatment of myasthenia gravis, chronic inflammatory
polyneuropathy and inclusion body myositis.
J Neurol Sci. 2001 Apr 1;185(2):119-22.
PMID: 11311292 [PubMed - indexed for MEDLINE]

335: Zanusso G, Vattemi G, Ferrari S, Tabaton M, Pecini E, Cavallaro T,
Tomelleri G, Filosto M, Tonin P, Nardelli E, Rizzuto N, Monaco S.
Increased expression of the normal cellular isoform of prion protein in
inclusion-body myositis, inflammatory myopathies and denervation atrophy.
Brain Pathol. 2001 Apr;11(2):182-9.
PMID: 11303793 [PubMed - indexed for MEDLINE]

336: Gurgel-Giannetti J, Reed U, Bang ML, Pelin K, Donner K, Marie SK, Carvalho
M, Fireman MA, Zanoteli E, Oliveira AS, Zatz M, Wallgren-Pettersson C, Labeit S,
Vainzof M.
Nebulin expression in patients with nemaline myopathy.
Neuromuscul Disord. 2001 Mar;11(2):154-62.
PMID: 11257471 [PubMed - indexed for MEDLINE]

337: Knowles CH, Nickols CD, Scott SM, Bennett NI, de Oliveira RB, Chimelli L,
Feakins R, Williams NS, Martin JE.
Smooth muscle inclusion bodies in slow transit constipation.
J Pathol. 2001 Mar;193(3):390-7.
PMID: 11241421 [PubMed - indexed for MEDLINE]

338: Arnardottir S, Ansved T, Nennesmo I, Borg K.
Report of a patient with inclusion body myositis and CD8+ chronic lymphocytic
leukaemia--post-mortem analysis of muscle and brain.
Acta Neurol Scand. 2001 Feb;103(2):131-5.
PMID: 11227133 [PubMed - indexed for MEDLINE]

339: Askanas V, Engel WK.
Inclusion-body myositis: newest concepts of pathogenesis and relation to aging
and Alzheimer disease.
J Neuropathol Exp Neurol. 2001 Jan;60(1):1-14. Review.
PMID: 11202170 [PubMed - indexed for MEDLINE]

340: Hardiman O.
Pitfalls in the diagnosis of motor neurone disease.
Hosp Med. 2000 Nov;61(11):767-71. Review.
PMID: 11198744 [PubMed - indexed for MEDLINE]

341: Yan C, Ikezoe K, Nonaka I.
Apoptotic muscle fiber degeneration in distal myopathy with rimmed vacuoles.
Acta Neuropathol (Berl). 2001 Jan;101(1):9-16.
PMID: 11194945 [PubMed - indexed for MEDLINE]

342: Dalakas MC, Koffman B, Fujii M, Spector S, Sivakumar K, Cupler E.
A controlled study of intravenous immunoglobulin combined with prednisone in
the treatment of IBM.
Neurology. 2001 Feb 13;56(3):323-7.
PMID: 11171896 [PubMed - indexed for MEDLINE]

343: Ozden S, Gessain A, Gout O, Mikol J.
Sporadic inclusion body myositis in a patient with human T cell leukemia virus
type 1-associated myelopathy.
Clin Infect Dis. 2001 Feb 1;32(3):510-4. Epub 2001 Jan 24.
PMID: 11170963 [PubMed - indexed for MEDLINE]

344: Muller-Felber W, Pongratz D, Reimers C.
64th ENMC International Workshop: therapeutic approaches to dermatomyositis,
polymyositis, and inclusion body myositis29-31 January 1999, Naarden, The
Netherlands.
Neuromuscul Disord. 2001 Jan;11(1):88-92. No abstract available.
PMID: 11166170 [PubMed - indexed for MEDLINE]

345: Voit T, Kutz P, Leube B, Neuen-Jacob E, Schroder JM, Cavallotti D,
Vaccario ML, Schaper J, Broich P, Cohn R, Baethmann M, Gohlich-Ratmann G,
Scoppetta C, Herrmann R.
Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus.
Neuromuscul Disord. 2001 Jan;11(1):11-9.
PMID: 11166161 [PubMed - indexed for MEDLINE]

346: Goebel HH, Warlo IA.
Surplus protein myopathies.
Neuromuscul Disord. 2001 Jan;11(1):3-6. Review.
PMID: 11166159 [PubMed - indexed for MEDLINE]

347: Corbett MA, Robinson CS, Dunglison GF, Yang N, Joya JE, Stewart AW,
Schnell C, Gunning PW, North KN, Hardeman EC.
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and
hypertrophy in a mouse model for nemaline myopathy.
Hum Mol Genet. 2001 Feb 15;10(4):317-28.
PMID: 11157795 [PubMed - indexed for MEDLINE]

348: Kieseier BC, Schneider C, Clements JM, Gearing AJ, Gold R, Toyka KV,
Hartung HP.
Expression of specific matrix metalloproteinases in inflammatory myopathies.
Brain. 2001 Feb;124(Pt 2):341-51.
PMID: 11157561 [PubMed - indexed for MEDLINE]

349: Brouwer R, Hengstman GJ, Vree Egberts W, Ehrfeld H, Bozic B, Ghirardello
A, Grondal G, Hietarinta M, Isenberg D, Kalden JR, Lundberg I, Moutsopoulos H,
Roux-Lombard P, Vencovsky J, Wikman A, Seelig HP, van Engelen BG, van Venrooij
WJ.
Autoantibody profiles in the sera of European patients with myositis.
Ann Rheum Dis. 2001 Feb;60(2):116-23.
PMID: 11156543 [PubMed - indexed for MEDLINE]

350: Abel A, Walcott J, Woods J, Duda J, Merry DE.
Expression of expanded repeat androgen receptor produces neurologic disease in
transgenic mice.
Hum Mol Genet. 2001 Jan 15;10(2):107-16.
PMID: 11152658 [PubMed - indexed for MEDLINE]

351: Hengstman GJ, van Engelen BG, ter Laak HJ, Gabreels-Festen AA.
Familial inclusion body myositis with histologically confirmed sensorimotor
axonal neuropathy.
J Neurol. 2000 Nov;247(11):882-4. No abstract available.
PMID: 11151424 [PubMed - indexed for MEDLINE]

352: Nakano S, Shinde A, Kawashima S, Nakamura S, Akiguchi I, Kimura J.
Inclusion body myositis: expression of extracellular signal-regulated kinase
and its substrate.
Neurology. 2001 Jan 9;56(1):87-93.
PMID: 11148241 [PubMed - indexed for MEDLINE]

353: Lundberg IE.
The role of cytokines, chemokines, and adhesion molecules in the pathogenesis
of idiopathic inflammatory myopathies.
Curr Rheumatol Rep. 2000 Jun;2(3):216-24. Review.
PMID: 11123062 [PubMed - indexed for MEDLINE]

354: Mastaglia FL, Phillips BA, Zilko PJ.
Inflammatory Myopathy.
Curr Treat Options Neurol. 1999 Jul;1(3):263-272.
PMID: 11096714 [PubMed - as supplied by publisher]

355: Shamim EA, Rider LG, Miller FW.
Update on the genetics of the idiopathic inflammatory myopathies.
Curr Opin Rheumatol. 2000 Nov;12(6):482-91. Review.
PMID: 11092196 [PubMed - indexed for MEDLINE]

356: Badrising UA, Maat-Schieman M, van Duinen SG, Breedveld F, van Doorn P,
van Engelen B, van den Hoogen F, Hoogendijk J, Howeler C, de Jager A, Jennekens
F, Koehler P, van der Leeuw H, de Visser M, Verschuuren JJ, Wintzen AR.
Epidemiology of inclusion body myositis in the Netherlands: a nationwide study.
Neurology. 2000 Nov 14;55(9):1385-7.
PMID: 11087787 [PubMed - indexed for MEDLINE]

357: Becher MW, Kotzuk JA, Davis LE, Bear DG.
Intranuclear inclusions in oculopharyngeal muscular dystrophy contain poly(A)
binding protein 2.
Ann Neurol. 2000 Nov;48(5):812-5.
PMID: 11079550 [PubMed - indexed for MEDLINE]

358: Bedlack RS, Strittmatter WJ, Morgenlander JC.
Apolipoprotein E and neuromuscular disease: a critical review of the
literature.
Arch Neurol. 2000 Nov;57(11):1561-5. Review.
PMID: 11074787 [PubMed - indexed for MEDLINE]

359: Orth M, Tabrizi SJ, Schapira AH.
Sporadic inclusion body myositis not linked to prion protein codon 129
methionine homozygosity.
Neurology. 2000 Oct 24;55(8):1235. No abstract available.
PMID: 11071511 [PubMed - indexed for MEDLINE]

360: Wilczynski GM, Engel WK, Askanas V.
Cyclin-dependent kinase 5 colocalizes with phosphorylated tau in human
inclusion-body myositis paired-helical filaments and may play a role in tau
phosphorylation.
Neurosci Lett. 2000 Oct 20;293(1):33-6.
PMID: 11065131 [PubMed - indexed for MEDLINE]

361: Vattemi G, Tonin P, Filosto M, Spagnolo M, Rizzuto N, Tomelleri G.
T-cell anti-apoptotic mechanisms in inflammatory myopathies.
J Neuroimmunol. 2000 Nov 1;111(1-2):146-51.
PMID: 11063832 [PubMed - indexed for MEDLINE]

362: Hermanns B, Molnar M, Schroder JM.
Peripheral neuropathy associated with hereditary and sporadic inclusion body
myositis: confirmation by electron microscopy and morphometry.
J Neurol Sci. 2000 Oct 1;179(S 1-2):92-102.
PMID: 11054491 [PubMed - indexed for MEDLINE]

363: Kok CC, Boyt A, Gaudieri S, Martins R, Askanas V, Dalakas M, Kiers L,
Mastaglia F, Garlepp M.
Mitochondrial DNA variants in inclusion body myositis.
Neuromuscul Disord. 2000 Dec;10(8):604-11.
PMID: 11053689 [PubMed - indexed for MEDLINE]

364: Amemiya K, Granger RP, Dalakas MC.
Clonal restriction of T-cell receptor expression by infiltrating lymphocytes in
inclusion body myositis persists over time. Studies in repeated muscle biopsies.
Brain. 2000 Oct;123 ( Pt 10):2030-9.
PMID: 11004120 [PubMed - indexed for MEDLINE]

365: Calado A, Tome FM, Brais B, Rouleau GA, Kuhn U, Wahle E, Carmo-Fonseca M.
Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A)
binding protein 2 aggregates which sequester poly(A) RNA.
Hum Mol Genet. 2000 Sep 22;9(15):2321-8.
PMID: 11001936 [PubMed - indexed for MEDLINE]

366: Goebel HH, Warlo I.
Gene-related protein surplus myopathies.
Mol Genet Metab. 2000 Sep-Oct;71(1-2):267-75. Review.
PMID: 11001821 [PubMed - indexed for MEDLINE]

367: Gause A, Inderrieden DC, Laas R, Arlt AC, Gross WL.
Common variable immunodeficiency (CVID) and inclusion body myositis (IBM).
Immunobiology. 2000 Aug;202(2):199-203.
PMID: 10993295 [PubMed - indexed for MEDLINE]

368: Grau JM, Perea M.
Dermatomyositis with the features of inclusion body myositis associated with
carcinoma of the bladder: a true association?
Br J Dermatol. 2000 Sep;143(3):671. No abstract available.
PMID: 10971365 [PubMed - indexed for MEDLINE]

369: Boon AJ, Stolp-Smith KA.
Inclusion body myositis masquerading as polymyositis: a case study.
Arch Phys Med Rehabil. 2000 Aug;81(8):1123-6.
PMID: 10943766 [PubMed - indexed for MEDLINE]

370: Mirabella M, Christodoulou K, Di Giovanni S, Ricci E, Tonali P, Servidei
S.
An Italian family with autosomal recessive quadriceps-sparing inclusion-body
myopathy (ARQS-IBM) linked to chromosome 9p1.
Neurol Sci. 2000 Apr;21(2):99-102.
PMID: 10938188 [PubMed - indexed for MEDLINE]

371: Evert BO, Wullner U, Klockgether T.
Cell death in polyglutamine diseases.
Cell Tissue Res. 2000 Jul;301(1):189-204. Review.
PMID: 10928291 [PubMed - indexed for MEDLINE]

372: de Palma L, Chillemi C, Albanelli S, Rapali S, Bertoni-Freddari C.
Muscle involvement in rheumatoid arthritis: an ultrastructural study.
Ultrastruct Pathol. 2000 May-Jun;24(3):151-6.
PMID: 10914426 [PubMed - indexed for MEDLINE]

373: Kawashima T, Furuta A, Doh-ura K, Kikuchi H, Iwaki T.
Ubiquitin-immunoreactive skein-like inclusions in the neostriatum are not
restricted to amyotrophic lateral sclerosis, but are rather aging-related
structures.
Acta Neuropathol (Berl). 2000 Jul;100(1):43-9.
PMID: 10912919 [PubMed - indexed for MEDLINE]

374: Jansson M, Darin N, Kyllerman M, Martinsson T, Wahlstrom J, Oldfors A.
Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.
Acta Neuropathol (Berl). 2000 Jul;100(1):23-8.
PMID: 10912916 [PubMed - indexed for MEDLINE]

375: Peng A, Koffman BM, Malley JD, Dalakas MC.
Disease progression in sporadic inclusion body myositis: observations in 78
patients.
Neurology. 2000 Jul 25;55(2):296-8.
PMID: 10908910 [PubMed - indexed for MEDLINE]

376: Askanas V, Engel WK, Alvarez RB, McFerrin J, Broccolini A.
Novel immunolocalization of alpha-synuclein in human muscle of inclusion-body
myositis, regenerating and necrotic muscle fibers, and at neuromuscular
junctions.
J Neuropathol Exp Neurol. 2000 Jul;59(7):592-8.
PMID: 10901230 [PubMed - indexed for MEDLINE]

377: Catoggio LJ, Soriano ER.
Inflammatory muscle disease: therapeutic aspects.
Baillieres Best Pract Res Clin Rheumatol. 2000 Mar;14(1):55-71.
PMID: 10882214 [PubMed - indexed for MEDLINE]

378: Wilczynski GM, Engel WK, Askanas V.
Association of active extracellular signal-regulated protein kinase with paired
helical filaments of inclusion-body myositis muscle suggests its role in
inclusion-body myositis tau phosphorylation.
Am J Pathol. 2000 Jun;156(6):1835-40.
PMID: 10854206 [PubMed - indexed for MEDLINE]

379: Di Blasi C, Mora M, Pareyson D, Farina L, Sghirlanzoni A, Vignier N,
Blasevich F, Cornelio F, Guicheney P, Morandi L.
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling
inclusion body myositis.
Ann Neurol. 2000 Jun;47(6):811-6.
PMID: 10852549 [PubMed - indexed for MEDLINE]

380: Phillips BA, Zilko PJ, Mastaglia FL.
Prevalence of sporadic inclusion body myositis in Western Australia.
Muscle Nerve. 2000 Jun;23(6):970-2.
PMID: 10842277 [PubMed - indexed for MEDLINE]

381: Broccolini A, Engel WK, Alvarez RB, Askanas V.
Redox factor-1 in muscle biopsies of patients with inclusion-body myositis.
Neurosci Lett. 2000 Jun 16;287(1):1-4.
PMID: 10841976 [PubMed - indexed for MEDLINE]

382: Limaye V, Scott G, Kwiatek R, Pile K.
Inclusion body myositis associated with systemic lupus erythematosus (SLE)
Aust N Z J Med. 2000 Apr;30(2):275-6. No abstract available.
PMID: 10833124 [PubMed - indexed for MEDLINE]

383: Li M, Dalakas MC.
Expression of human IAP-like protein in skeletal muscle: a possible explanation
for the rare incidence of muscle fiber apoptosis in T-cell mediated inflammatory
myopathies.
J Neuroimmunol. 2000 Jul 1;106(1-2):1-5.
PMID: 10814776 [PubMed - indexed for MEDLINE]

384: Guyer C.
Recent developments in animal models of human neurodegenerative diseases.
Toxicol Pathol. 2000 Mar-Apr;28(2):363-6. No abstract available.
PMID: 10805156 [PubMed - indexed for MEDLINE]

385: Probst A, Gotz J, Wiederhold KH, Tolnay M, Mistl C, Jaton AL, Hong M,
Ishihara T, Lee VM, Trojanowski JQ, Jakes R, Crowther RA, Spillantini MG, Burki
K, Goedert M.
Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein.
Acta Neuropathol (Berl). 2000 May;99(5):469-81.
PMID: 10805089 [PubMed - indexed for MEDLINE]

386: Nagaraju K, Casciola-Rosen L, Rosen A, Thompson C, Loeffler L, Parker T,
Danning C, Rochon PJ, Gillespie J, Plotz P.
The inhibition of apoptosis in myositis and in normal muscle cells.
J Immunol. 2000 May 15;164(10):5459-65.
PMID: 10799913 [PubMed - indexed for MEDLINE]

387: Illa I.
Distal myopathies.
J Neurol. 2000 Mar;247(3):169-74. Review.
PMID: 10787109 [PubMed - indexed for MEDLINE]

388: Gayathri N, Anisya-Vasanth, Veerendra Kumar M, Das S, Santosh V, Yasha TC,
Ramamohan Y, Taly AB, Gourie-Devi M, Shankar SK.
Inclusion body myositis (IBM).
Clin Neuropathol. 2000 Jan-Feb;19(1):13-20.
PMID: 10774946 [PubMed - indexed for MEDLINE]

389: Garlepp MJ, Mastaglia FL.
Autoantibodies in inflammatory myopathies.
Am J Med Sci. 2000 Apr;319(4):227-33. Review. No abstract available.
PMID: 10768607 [PubMed - indexed for MEDLINE]

390: Li M, Dalakas MC.
The muscle mitogen-activated protein kinase is altered in sporadic inclusion
body myositis.
Neurology. 2000 Apr 25;54(8):1665-70.
PMID: 10762511 [PubMed - indexed for MEDLINE]

391: Askanas V, Engel WK, Alvarez RB, Frangione B, Ghiso J, Vidal R.
Inclusion body myositis, muscle blood vessel and cardiac amyloidosis, and
transthyretin Val122Ile allele.
Ann Neurol. 2000 Apr;47(4):544-9.
PMID: 10762172 [PubMed - indexed for MEDLINE]

392: Broccolini A, Engel WK, Alvarez RB, Askanas V.
Paired helical filaments of inclusion-body myositis muscle contain RNA and
survival motor neuron protein.
Am J Pathol. 2000 Apr;156(4):1151-5.
PMID: 10751338 [PubMed - indexed for MEDLINE]

393: Confalonieri P, Bernasconi P, Megna P, Galbiati S, Cornelio F, Mantegazza
R.
Increased expression of beta-chemokines in muscle of patients with inflammatory
myopathies.
J Neuropathol Exp Neurol. 2000 Feb;59(2):164-9.
PMID: 10749105 [PubMed - indexed for MEDLINE]

394: Choi YC, Park GT, Kim TS, Sunwoo IN, Steinert PM, Kim SY.
Sporadic inclusion body myositis correlates with increased expression and
cross-linking by transglutaminases 1 and 2.
J Biol Chem. 2000 Mar 24;275(12):8703-10.
PMID: 10722712 [PubMed - indexed for MEDLINE]

395: Banwell BL, Engel AG.
AlphaB-crystallin immunolocalization yields new insights into inclusion body
myositis.
Neurology. 2000 Mar 14;54(5):1033-41.
PMID: 10720271 [PubMed - indexed for MEDLINE]

396: Karpati G, Hohlfeld R.
Biologically stressed muscle fibers in sporadic IBM: a clue for the enigmatic
etiology?
Neurology. 2000 Mar 14;54(5):1020-1. No abstract available.
PMID: 10720268 [PubMed - indexed for MEDLINE]

397: Walter MC, Lochmuller H, Toepfer M, Schlotter B, Reilich P, Schroder M,
Muller-Felber W, Pongratz D.
High-dose immunoglobulin therapy in sporadic inclusion body myositis: a
double-blind, placebo-controlled study.
J Neurol. 2000 Jan;247(1):22-8.
PMID: 10701893 [PubMed - indexed for MEDLINE]

398: Capsoni S, Ruberti F, Di Daniel E, Cattaneo A.
Muscular dystrophy in adult and aged anti-NGF transgenic mice resembles an
inclusion body myopathy.
J Neurosci Res. 2000 Feb 15;59(4):553-60.
PMID: 10679795 [PubMed - indexed for MEDLINE]

399: Baron P, Galimberti D, Meda L, Prat E, Scarpini E, Conti G, Moggio M,
Prelle A, Scarlato G.
Synergistic effect of beta-amyloid protein and interferon gamma on nitric oxide
production by C2C12 muscle cells.
Brain. 2000 Feb;123 ( Pt 2):374-9.
PMID: 10648444 [PubMed - indexed for MEDLINE]

400: Nakayama T, Horiuchi E, Watanabe T, Murayama S, Nakase H.
A case of inclusion body myositis with benign monoclonal gammopathy
successfully responding to repeated immunoabsorption.
J Neurol Neurosurg Psychiatry. 2000 Feb;68(2):230-3.
PMID: 10644796 [PubMed - indexed for MEDLINE]

401: Amemiya K, Semino-Mora C, Granger RP, Dalakas MC.
Downregulation of TGF-beta1 mRNA and protein in the muscles of patients with
inflammatory myopathies after treatment with high-dose intravenous
immunoglobulin.
Clin Immunol. 2000 Feb;94(2):99-104.
PMID: 10637094 [PubMed - indexed for MEDLINE]

402: Choi YC, Dalakas MC.
Expression of matrix metalloproteinases in the muscle of patients with
inflammatory myopathies.
Neurology. 2000 Jan 11;54(1):65-71.
PMID: 10636127 [PubMed - indexed for MEDLINE]

403: Martinsson T, Oldfors A, Darin N, Berg K, Tajsharghi H, Kyllerman M,
Wahlstrom J.
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin
heavy chain IIa gene.
Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14614-9.
PMID: 11114175 [PubMed - indexed for MEDLINE]

404: Mirabella M, Di Giovanni S, Silvestri G, Tonali P, Servidei S.
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA
mutations: a potential pathogenic mechanism.
Brain. 2000 Jan;123 ( Pt 1):93-104.
PMID: 10611124 [PubMed - indexed for MEDLINE]

405: McFerrin J, Engel WK, Askanas V.
Cultured inclusion-body myositis muscle fibers do not accumulate beta-amyloid
precursor protein and can be innervated.
Neurology. 1999 Dec 10;53(9):2184-7.
PMID: 10599804 [PubMed - indexed for MEDLINE]

406: Dourmishev AL, Dourmishev LA.
Dermatomyositis and drugs.
Adv Exp Med Biol. 1999;455:187-91. Review.
PMID: 10599342 [PubMed - indexed for MEDLINE]

407: Krajnc I.
Dermatomyositis. Diagnosis and evaluation of dermatomyositis, polymyositis, and
inclusion-body myositis.
Adv Exp Med Biol. 1999;455:181-6. Review.
PMID: 10599341 [PubMed - indexed for MEDLINE]

408: Ishihara T, Hong M, Zhang B, Nakagawa Y, Lee MK, Trojanowski JQ, Lee VM.
Age-dependent emergence and progression of a tauopathy in transgenic mice
overexpressing the shortest human tau isoform.
Neuron. 1999 Nov;24(3):751-62.
PMID: 10595524 [PubMed - indexed for MEDLINE]

409: Oldfors A, Lindberg C.
Inclusion body myositis.
Curr Opin Neurol. 1999 Oct;12(5):527-33. Review.
PMID: 10590889 [PubMed - indexed for MEDLINE]

410: Nonaka I.
Distal myopathies.
Curr Opin Neurol. 1999 Oct;12(5):493-9. Review.
PMID: 10590885 [PubMed - indexed for MEDLINE]

411: Megens-de Letter MA, Visser LH, van Doorn PA, Savelkoul HF.
Cytokines in the muscle tissue of idiopathic inflammatory myopathies:
implications for immunopathogenesis and therapy.
Eur Cytokine Netw. 1999 Dec;10(4):471-8. Review.
PMID: 10586113 [PubMed - indexed for MEDLINE]

412: Talanin NY, Bushore D, Rasberry R, Rudolph T, Tuli M, Friedman-Musicante
R.
Dermatomyositis with the features of inclusion body myositis associated with
carcinoma of the bladder.
Br J Dermatol. 1999 Nov;141(5):926-30.
PMID: 10583182 [PubMed - indexed for MEDLINE]

413: Webster G, Beynon H.
Weak at the knees.
Lancet. 1999 Nov 13;354(9191):1696. No abstract available.
PMID: 10568573 [PubMed - indexed for MEDLINE]

414: Nakano S, Akiguchi I, Nakamura S, Satoi H, Kawashima S, Kimura J.
Aberrant expression of cyclin-dependent kinase 5 in inclusion body myositis.
Neurology. 1999 Nov 10;53(8):1671-6.
PMID: 10563611 [PubMed - indexed for MEDLINE]

415: Cherin P.
Treatment of inclusion body myositis.
Curr Opin Rheumatol. 1999 Nov;11(6):456-61. Review.
PMID: 10551668 [PubMed - indexed for MEDLINE]

416: Buchholz DW, Neumann S.
Dysphagia in patients with inclusion body myositis.
Dysphagia. 1999 Summer;14(3):187. No abstract available.
PMID: 10507903 [PubMed - indexed for MEDLINE]

417: Servidei S, Capon F, Spinazzola A, Mirabella M, Semprini S, de Rosa G,
Gennarelli M, Sangiuolo F, Ricci E, Mohrenweiser HW, Dallapiccola B, Tonali P,
Novelli G.
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.
Neurology. 1999 Sep 11;53(4):830-7.
PMID: 10489050 [PubMed - indexed for MEDLINE]

418: Naumann M, Toyka KV.
Inclusion body myositis in twins.
Neurology. 1999 Aug 11;53(3):659. No abstract available.
PMID: 10449152 [PubMed - indexed for MEDLINE]

419: Murata K, Dalakas MC.
Expression of the costimulatory molecule BB-1, the ligands CTLA-4 and CD28, and
their mRNA in inflammatory myopathies.
Am J Pathol. 1999 Aug;155(2):453-60.
PMID: 10433938 [PubMed - indexed for MEDLINE]

420: De Bleecker JL, Meire VI, Declercq W, Van Aken EH.
Immunolocalization of tumor necrosis factor-alpha and its receptors in
inflammatory myopathies.
Neuromuscul Disord. 1999 Jun;9(4):239-46.
PMID: 10399751 [PubMed - indexed for MEDLINE]

421: Olive M, Ferrer I.
Bcl-2 and Bax protein expression in human myopathies.
J Neurol Sci. 1999 Mar 15;164(1):76-81.
PMID: 10385052 [PubMed - indexed for MEDLINE]

422: Kok CC, Croager EJ, Witt CS, Kiers L, Mastaglia FL, Abraham LJ, Garlepp
MJ.
Mapping of a candidate region for susceptibility to inclusion body myositis in
the human major histocompatibility complex.
Immunogenetics. 1999 Jun;49(6):508-16.
PMID: 10380695 [PubMed - indexed for MEDLINE]

423: Liprandi A, Bartoli C, Figarella-Branger D, Pellissier JF, Lepidi H.
Local expression of monocyte chemoattractant protein-1 (MCP-1) in idiopathic
inflammatory myopathies.
Acta Neuropathol (Berl). 1999 Jun;97(6):642-8.
PMID: 10378384 [PubMed - indexed for MEDLINE]

424: Morris HR, Landon D, Morgan-Hughes J, Brown P.
Late-onset cytoplasmic body myopathy resembling myotonic dystrophy.
Muscle Nerve. 1999 Jun;22(6):781-2. No abstract available.
PMID: 10366237 [PubMed - indexed for MEDLINE]

425: McCoy AL, Bubb MR, Plotz PH, Davis JC.
Inclusion body myositis long after dermatomyositis: a report of two cases.
Clin Exp Rheumatol. 1999 Mar-Apr;17(2):235-9.
PMID: 10342053 [PubMed - indexed for MEDLINE]

426: Fidzianska A, Drac H, Kaminska AM.
Familial inclusion body myopathy with desmin storage.
Acta Neuropathol (Berl). 1999 May;97(5):509-14.
PMID: 10334489 [PubMed - indexed for MEDLINE]

427: Martinsson T, Darin N, Kyllerman M, Oldfors A, Hallberg B, Wahlstrom J.
Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome
region 17p13.1.
Am J Hum Genet. 1999 May;64(5):1420-6.
PMID: 10205275 [PubMed - indexed for MEDLINE]

428: Barkhaus PE, Periquet MI, Nandedkar SD.
Quantitative electrophysiologic studies in sporadic inclusion body myositis.
Muscle Nerve. 1999 Apr;22(4):480-7.
PMID: 10204783 [PubMed - indexed for MEDLINE]

429: Mizukami K, Sasaki M, Baba A, Suzuki T, Shiraishi H.
An autopsy case of myotonic dystrophy with mental disorders and various
neuropathologic features.
Psychiatry Clin Neurosci. 1999 Feb;53(1):51-5.
PMID: 10201284 [PubMed - indexed for MEDLINE]

430: Render JA, Common RS, Kennedy FA, Jones MZ, Fyfe JC.
Amylopectinosis in fetal and neonatal Quarter Horses.
Vet Pathol. 1999 Mar;36(2):157-60.
PMID: 10098645 [PubMed - indexed for MEDLINE]

431: Caron A, Gohel C, Mollaret K, Morello R, Chapon F.
Study of some components of the cytoskeleton in muscular disorders with
nonspecific cytoplasmic bodies.
Acta Neuropathol (Berl). 1999 Mar;97(3):267-74.
PMID: 10090674 [PubMed - indexed for MEDLINE]

432: Huang CC, Chu CC, Pang CY, Wei YH.
Tissue mosaicism in the skeletal muscle and sural nerve biopsies in the MELAS
syndrome.
Acta Neurol Scand. 1999 Feb;99(2):125-9.
PMID: 10071173 [PubMed - indexed for MEDLINE]

433: Mezei MM, Mankodi A, Brais B, Marineau C, Thornton CA, Rouleau GA, Karpati
G.
Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to
sporadic inclusion body myositis.
Neurology. 1999 Feb;52(3):669-70. No abstract available.
PMID: 10025815 [PubMed - indexed for MEDLINE]

434: Lampe J, Kitzler H, Walter MC, Lochmuller H, Reichmann H.
Methionine homozygosity at prion gene codon 129 may predispose to sporadic
inclusion-body myositis.
Lancet. 1999 Feb 6;353(9151):465-6. No abstract available.
PMID: 9989722 [PubMed - indexed for MEDLINE]

435: Furuoka H, Murakami A, Doi T, Kobayashi Y, Matsui T, Nakamura N.
Immunohistochemical and electron microscopical studies of myocardial inclusions
in hereditary myopathy of the diaphragmatic muscles in Holstein-Friesian cattle.
Acta Neuropathol (Berl). 1999 Feb;97(2):185-91.
PMID: 9928830 [PubMed - indexed for MEDLINE]

436: Eisenberg I, Thiel C, Levi T, Tiram E, Argov Z, Sadeh M, Jackson CL,
Thierfelder L, Mitrani-Rosenbaum S.
Fine-structure mapping of the hereditary inclusion body myopathy locus.
Genomics. 1999 Jan 1;55(1):43-8.
PMID: 9888997 [PubMed - indexed for MEDLINE]

437: Vogel H.
Inclusion body myositis--a review.
Adv Anat Pathol. 1998 May;5(3):164-9. Review.
PMID: 9868522 [PubMed - indexed for MEDLINE]

438: Dalakas MC.
Molecular immunology and genetics of inflammatory muscle diseases.
Arch Neurol. 1998 Dec;55(12):1509-12. Review.
PMID: 9865793 [PubMed - indexed for MEDLINE]

439: Hutchinson DO.
Inclusion body myositis: abnormal protein accumulation does not trigger
apoptosis.
Neurology. 1998 Dec;51(6):1742-5.
PMID: 9855538 [PubMed - indexed for MEDLINE]

440: Askanas V, Engel WK.
Sporadic inclusion-body myositis and its similarities to Alzheimer disease
brain. Recent approaches to diagnosis and pathogenesis, and relation to aging.
Scand J Rheumatol. 1998;27(6):389-405. Review.
PMID: 9855208 [PubMed - indexed for MEDLINE]

441: Dalakas MC.
Controlled studies with high-dose intravenous immunoglobulin in the treatment
of dermatomyositis, inclusion body myositis, and polymyositis.
Neurology. 1998 Dec;51(6 Suppl 5):S37-45. Review.
PMID: 9851729 [PubMed - indexed for MEDLINE]

442: Rowland LP.
Diagnosis of amyotrophic lateral sclerosis.
J Neurol Sci. 1998 Oct;160 Suppl 1:S6-24. Review.
PMID: 9851643 [PubMed - indexed for MEDLINE]

443: Tome FM, Fardeau M.
Hereditary inclusion body myopathies.
Curr Opin Neurol. 1998 Oct;11(5):453-9. Review.
PMID: 9847994 [PubMed - indexed for MEDLINE]

444: Fyhr IM, Moslemi AR, Lindberg C, Oldfors A.
T cell receptor beta-chain repertoire in inclusion body myositis.
J Neuroimmunol. 1998 Nov 2;91(1-2):129-34.
PMID: 9846829 [PubMed - indexed for MEDLINE]

445: Fukuchi K, Pham D, Hart M, Li L, Lindsey JR.
Amyloid-beta deposition in skeletal muscle of transgenic mice: possible model
of inclusion body myopathy.
Am J Pathol. 1998 Dec;153(6):1687-93.
PMID: 9846958 [PubMed - indexed for MEDLINE]

446: Jin LW, Hearn MG, Ogburn CE, Dang N, Nochlin D, Ladiges WC, Martin GM.
Transgenic mice over-expressing the C-99 fragment of betaPP with an
alpha-secretase site mutation develop a myopathy similar to human inclusion body
myositis.
Am J Pathol. 1998 Dec;153(6):1679-86.
PMID: 9846957 [PubMed - indexed for MEDLINE]

447: Askanas V, Engel WK.
Does overexpression of betaAPP in aging muscle have a pathogenic role and a
relevance to Alzheimer's disease? Clues from inclusion body myositis, cultured
human muscle, and transgenic mice.
Am J Pathol. 1998 Dec;153(6):1673-7. No abstract available.
PMID: 9846956 [PubMed - indexed for MEDLINE]

448: Levine TD, Pestronk A.
Inflammatory myopathy with cytochrome oxidase negative muscle fibers:
methotrexate treatment.
Muscle Nerve. 1998 Dec;21(12):1724-8.
PMID: 9843075 [PubMed - indexed for MEDLINE]

449: Johannes S, Schubert M, Heidenreich F, Walter GF, Dengler R.
Inclusion body myositis: immune globulins improve muscle strength, but not
abnormal postures.
J Neurol. 1998 Dec;245(12):816-8. No abstract available.
PMID: 9840358 [PubMed - indexed for MEDLINE]

450: Behrens L, Kerschensteiner M, Misgeld T, Goebels N, Wekerle H, Hohlfeld R.

Human muscle cells express a functional costimulatory molecule distinct from
B7.1 (CD80) and B7.2 (CD86) in vitro and in inflammatory lesions.
J Immunol. 1998 Dec 1;161(11):5943-51. Erratum in: J Immunol 2000 May
15;164(10):5330.
PMID: 9834075 [PubMed - indexed for MEDLINE]

451: McFerrin J, Engel WK, Askanas V.
Impaired innervation of cultured human muscle overexpressing betaAPP
experimentally and genetically: relevance to inclusion-body myopathies.
Neuroreport. 1998 Oct 5;9(14):3201-5.
PMID: 9831451 [PubMed - indexed for MEDLINE]

452: Penisson-Besnier I, Dumez C, Chateau D, Dubas F, Fardeau M.
Autosomal dominant late adult onset distal leg myopathy.
Neuromuscul Disord. 1998 Oct;8(7):459-66.
PMID: 9829275 [PubMed - indexed for MEDLINE]

453: Lodi R, Taylor DJ, Tabrizi SJ, Hilton-Jones D, Squier MV, Seller A, Styles
P, Schapira AH.
Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body
myositis assessed by 31P-magnetic resonance spectroscopy.
Brain. 1998 Nov;121 ( Pt 11):2119-26.
PMID: 9827771 [PubMed - indexed for MEDLINE]

454: Argov Z, Eisenberg I, Mitrani-Rosenbaum S.
Genetics of inclusion body myopathies.
Curr Opin Rheumatol. 1998 Nov;10(6):543-7. Review.
PMID: 9812214 [PubMed - indexed for MEDLINE]

455: Askanas V, Engel WK.
Sporadic inclusion-body myositis and hereditary inclusion-body myopathies:
current concepts of diagnosis and pathogenesis.
Curr Opin Rheumatol. 1998 Nov;10(6):530-42. Review.
PMID: 9812213 [PubMed - indexed for MEDLINE]

456: Lundberg IE, Nyberg P.
New developments in the role of cytokines and chemokines in inflammatory
myopathies.
Curr Opin Rheumatol. 1998 Nov;10(6):521-9. Review.
PMID: 9812212 [PubMed - indexed for MEDLINE]

457: Bertorini TE.
Inflammatory myopathies [polymyositis, dermatomyositis, inclusion body
myositis]
Compr Ther. 1998 Oct;24(10):494-502. Review.
PMID: 9801848 [PubMed - indexed for MEDLINE]

458: Semino-Mora C, Dalakas MC.
Rimmed vacuoles with beta-amyloid and ubiquitinated filamentous deposits in the
muscles of patients with long-standing denervation (postpoliomyelitis muscular
atrophy): similarities with inclusion body myositis.
Hum Pathol. 1998 Oct;29(10):1128-33.
PMID: 9781653 [PubMed - indexed for MEDLINE]

459: Yang CC, Askanas V, Engel WK, Alvarez RB.
Immunolocalization of transcription factor NF-kappaB in inclusion-body myositis
muscle and at normal human neuromuscular junctions.
Neurosci Lett. 1998 Sep 25;254(2):77-80.
PMID: 9779924 [PubMed - indexed for MEDLINE]

460: Illa I, Dalakas MC.
Dermatomyositis, polymyositis and inclusion body myositis: current concepts.
Rev Neurol (Paris). 1998 Jan;154(1):13-6. Review. No abstract available.
PMID: 9773019 [PubMed - indexed for MEDLINE]

461: Argov Z, Taivassalo T, De Stefano N, Genge A, Karpati G, Arnold DL.
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance
spectroscopy study.
Muscle Nerve. 1998 Nov;21(11):1523-5.
PMID: 9771678 [PubMed - indexed for MEDLINE]

462: Hengstman GJ, van Engelen BG, Badrising UA, van den Hoogen FH, van
Venrooij WJ.
Presence of the anti-Jo-1 autoantibody excludes inclusion body myositis.
Ann Neurol. 1998 Sep;44(3):423. No abstract available.
PMID: 9749616 [PubMed - indexed for MEDLINE]

463: Vajsar J, Balslev T, Ray PN, Siegel-Bartelt J, Jay V.
Congenital cytoplasmic body myopathy with survival motor neuron gene deletion
or Werdnig-Hoffmann disease.
Neurology. 1998 Sep;51(3):873-5.
PMID: 9748045 [PubMed - indexed for MEDLINE]

464: Amato AA, Shebert RT.
Inclusion body myositis in twins.
Neurology. 1998 Aug;51(2):598-600.
PMID: 9710045 [PubMed - indexed for MEDLINE]

465: Darin N, Kyllerman M, Wahlstrom J, Martinsson T, Oldfors A.
Autosomal dominant myopathy with congenital joint contractures,
ophthalmoplegia, and rimmed vacuoles.
Ann Neurol. 1998 Aug;44(2):242-8.
PMID: 9708547 [PubMed - indexed for MEDLINE]

466: Oyama F, Murakami N, Ihara Y.
Chloroquine myopathy suggests that tau is degraded in lysosomes: implication
for the formation of paired helical filaments in Alzheimer's disease.
Neurosci Res. 1998 May;31(1):1-8. Review.
PMID: 9704973 [PubMed - indexed for MEDLINE]

467: Molnar M, Schroder JM.
Pleomorphic mitochondrial and different filamentous inclusions in inflammatory
myopathies associated with mtDNA deletions.
Acta Neuropathol (Berl). 1998 Jul;96(1):41-51.
PMID: 9678512 [PubMed - indexed for MEDLINE]

468: Askanas V, Engel WK.
Sporadic inclusion-body myositis and hereditary inclusion-body myopathies:
diseases of oxidative stress and aging?
Arch Neurol. 1998 Jul;55(7):915-20. Review. No abstract available.
PMID: 9678308 [PubMed - indexed for MEDLINE]

469: Nonaka I, Murakami N, Suzuki Y, Kawai M.
Distal myopathy with rimmed vacuoles.
Neuromuscul Disord. 1998 Jun;8(5):333-7.
PMID: 9673988 [PubMed - indexed for MEDLINE]

470: Barohn RJ, Amato AA, Griggs RC.
Overview of distal myopathies: from the clinical to the molecular.
Neuromuscul Disord. 1998 Jun;8(5):309-16. Review.
PMID: 9673984 [PubMed - indexed for MEDLINE]

471: Askanas V, Engel WK, Alvarez RB.
Fourteen newly recognized proteins at the human neuromuscular junctions--and
their nonjunctional accumulation in inclusion-body myositis.
Ann N Y Acad Sci. 1998 May 13;841:28-56. Review. No abstract available.
PMID: 9668220 [PubMed - indexed for MEDLINE]

472: Mastaglia FL, Phillips BA, Zilko PJ.
Immunoglobulin therapy in inflammatory myopathies.
J Neurol Neurosurg Psychiatry. 1998 Jul;65(1):107-10.
PMID: 9667570 [PubMed - indexed for MEDLINE]

473: Houser SM, Calabrese LH, Strome M.
Dysphagia in patients with inclusion body myositis.
Laryngoscope. 1998 Jul;108(7):1001-5.
PMID: 9665246 [PubMed - indexed for MEDLINE]

474: Yang CC, Alvarez RB, Engel WK, Heller SL, Askanas V.
Nitric oxide-induced oxidative stress in autosomal recessive and dominant
inclusion-body myopathies.
Brain. 1998 Jun;121 ( Pt 6):1089-97.
PMID: 9648544 [PubMed - indexed for MEDLINE]

475: Tews DS, Goebel HH.
Cell death and oxidative damage in inflammatory myopathies.
Clin Immunol Immunopathol. 1998 Jun;87(3):240-7.
PMID: 9646833 [PubMed - indexed for MEDLINE]

476: Argov Z, Sadeh M, Eisenberg I, Karpati G, Mitrani-Rosenbaum S.
Facial weakness in hereditary inclusion body myopathies.
Neurology. 1998 Jun;50(6):1925-6. No abstract available.
PMID: 9633772 [PubMed - indexed for MEDLINE]

477: Veinot JP, Mai KT, Zarychanski R.
Chloroquine related cardiac toxicity.
J Rheumatol. 1998 Jun;25(6):1221-5.
PMID: 9632091 [PubMed - indexed for MEDLINE]

478: Goebel HH.
Congenital myopathies with inclusion bodies: a brief review.
Neuromuscul Disord. 1998 May;8(3-4):162-8. Review.
PMID: 9631396 [PubMed - indexed for MEDLINE]

479: Koffman BM, Sivakumar K, Simonis T, Stroncek D, Dalakas MC.
HLA allele distribution distinguishes sporadic inclusion body myositis from
hereditary inclusion body myopathies.

J Neuroimmunol. 1998 Apr 15;84(2):139-42.
PMID: 9628455 [PubMed - indexed for MEDLINE]

480: Bernasconi P, Confalonieri P, Andreetta F, Baggi F, Cornelio F, Mantegazza
R.
The expression of co-stimulatory and accessory molecules on cultured human
muscle cells is not dependent on stimulus by pro-inflammatory cytokines:
relevance for the pathogenesis of inflammatory myopathy.
J Neuroimmunol. 1998 May 1;85(1):52-8.
PMID: 9626997 [PubMed - indexed for MEDLINE]

481: Uyama E, Uchino M, Chateau D, Tome FM.
Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy
with rimmed vacuoles and oculopharyngeal muscular dystrophy.
Neuromuscul Disord. 1998 Apr;8(2):119-25.
PMID: 9608566 [PubMed - indexed for MEDLINE]

482: Borg K, Ahlberg G, Anvret M, Edstrom L.
Welander distal myopathy--an overview.
Neuromuscul Disord. 1998 Apr;8(2):115-8. Review.
PMID: 9608565 [PubMed - indexed for MEDLINE]

483: Ahlberg G, Borg K, Edstrom L, Anvret M.
Welander hereditary distal myopathy, a molecular genetic comparison to
hereditary myopathies with inclusion bodies.
Neuromuscul Disord. 1998 Apr;8(2):111-4.
PMID: 9608564 [PubMed - indexed for MEDLINE]

484: Bender A, Behrens L, Engel AG, Hohlfeld R.
T-cell heterogeneity in muscle lesions of inclusion body myositis.
J Neuroimmunol. 1998 Apr 1;84(1):86-91.
PMID: 9600712 [PubMed - indexed for MEDLINE]

485: Horvath R, Fu K, Johns T, Genge A, Karpati G, Shoubridge EA.
Characterization of the mitochondrial DNA abnormalities in the skeletal muscle
of patients with inclusion body myositis.
J Neuropathol Exp Neurol. 1998 May;57(5):396-403.
PMID: 9596410 [PubMed - indexed for MEDLINE]

486: Felice KJ, Relva GM, Conway SR.
Further observations on forearm flexor weakness in inclusion body myositis.
Muscle Nerve. 1998 May;21(5):659-61.
PMID: 9572250 [PubMed - indexed for MEDLINE]

487: Rider LG, Gurley RC, Pandey JP, Garcia de la Torre I, Kalovidouris AE,
O'Hanlon TP, Love LA, Hennekam RC, Baumbach LL, Neville HE, Garcia CA, Klingman
J, Gibbs M, Weisman MH, Targoff IN, Miller FW.
Clinical, serologic, and immunogenetic features of familial idiopathic
inflammatory myopathy.
Arthritis Rheum. 1998 Apr;41(4):710-9.
PMID: 9550481 [PubMed - indexed for MEDLINE]

488: Lepidi H, Frances V, Figarella-Branger D, Bartoli C, Machado-Baeta A,
Pellissier JF.
Local expression of cytokines in idiopathic inflammatory myopathies.
Neuropathol Appl Neurobiol. 1998 Feb;24(1):73-9.
PMID: 9549732 [PubMed - indexed for MEDLINE]

489: Askanas V, Engel WK, Yang CC, Alvarez RB, Lee VM, Wisniewski T.
Light and electron microscopic immunolocalization of presenilin 1 in abnormal
muscle fibers of patients with sporadic inclusion-body myositis and
autosomal-recessive inclusion-body myopathy.
Am J Pathol. 1998 Apr;152(4):889-95.
PMID: 9546349 [PubMed - indexed for MEDLINE]

490: van der Meulen MF, Hoogendijk JE, Jansen GH, Veldman H, Wokke JH.
Absence of characteristic features in two patients with inclusion body
myositis.
J Neurol Neurosurg Psychiatry. 1998 Mar;64(3):396-8.
PMID: 9527159 [PubMed - indexed for MEDLINE]

491: Hohlfeld R, Engel AG, Goebels N, Behrens L.
Cellular immune mechanisms in inflammatory myopathies.
Curr Opin Rheumatol. 1997 Nov;9(6):520-6. Review.
PMID: 9375281 [PubMed - indexed for MEDLINE]

492: Fyhr IM, Oldfors A.
Upregulation of Fas/Fas ligand in inclusion body myositis.
Ann Neurol. 1998 Jan;43(1):127-30.
PMID: 9450780 [PubMed - indexed for MEDLINE]

493: Koffman BM, Rugiero M, Dalakas MC.
Immune-mediated conditions and antibodies associated with sporadic inclusion
body myositis.
Muscle Nerve. 1998 Jan;21(1):115-7.
PMID: 9427231 [PubMed - indexed for MEDLINE]

494: Brannagan TH, Hays AP, Lange DJ, Trojaborg W.
The role of quantitative electromyography in inclusion body myositis.
J Neurol Neurosurg Psychiatry. 1997 Dec;63(6):776-9.
PMID: 9416815 [PubMed - indexed for MEDLINE]

495: Fyhr IM, Moslemi AR, Mosavi AA, Lindberg C, Tarkowski A, Oldfors A.
Oligoclonal expansion of muscle infiltrating T cells in inclusion body
myositis.
J Neuroimmunol. 1997 Nov;79(2):185-9.
PMID: 9394791 [PubMed - indexed for MEDLINE]

496: Spuler S, Engel AG.
SMI-31 immunoreactivity in inclusion body myositis.
Ann Neurol. 1997 Nov;42(5):815. No abstract available.
PMID: 9392584 [PubMed - indexed for MEDLINE]

497: Tome FM, Chateau D, Helbling-Leclerc A, Fardeau M.
Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy.
Neuromuscul Disord. 1997 Oct;7 Suppl 1:S63-9.
PMID: 9392019 [PubMed - indexed for MEDLINE]

498: Meola G, Sansone V, Rotondo G, Tome FM, Bouchard JP.
Oculopharyngeal muscular dystrophy in Italy.
Neuromuscul Disord. 1997 Oct;7 Suppl 1:S53-6.
PMID: 9392017 [PubMed - indexed for MEDLINE]

499: Medici M, Pizzarossa C, Skuk D, Yorio D, Emmanuelli G, Mesa R.
Oculopharyngeal muscular dystrophy in Uruguay.
Neuromuscul Disord. 1997 Oct;7 Suppl 1:S50-2.
PMID: 9392016 [PubMed - indexed for MEDLINE]

500: Spector SA, Lemmer JT, Koffman BM, Fleisher TA, Feuerstein IM, Hurley BF,
Dalakas MC.
Safety and efficacy of strength training in patients with sporadic inclusion
body myositis.
Muscle Nerve. 1997 Oct;20(10):1242-8.
PMID: 9324080 [PubMed - indexed for MEDLINE]

501: Goebel HH.
Desmin-related myopathies.
Curr Opin Neurol. 1997 Oct;10(5):426-9. Review.
PMID: 9330890 [PubMed - indexed for MEDLINE]

502: Sivakumar K, Dalakas MC.
Inclusion body myositis and myopathies.
Curr Opin Neurol. 1997 Oct;10(5):413-20. Review.
PMID: 9330888 [PubMed - indexed for MEDLINE]

503: O'Gorman E, Piendl T, Muller M, Brdiczka D, Wallimann T.
Mitochondrial intermembrane inclusion bodies: the common denominator between
human mitochondrial myopathies and creatine depletion, due to impairment of
cellular energetics.
Mol Cell Biochem. 1997 Sep;174(1-2):283-9.
PMID: 9309701 [PubMed - indexed for MEDLINE]

504: Schroder JM, Molnar M.
Mitochondrial abnormalities and peripheral neuropathy in inflammatory myopathy,
especially inclusion body myositis.
Mol Cell Biochem. 1997 Sep;174(1-2):277-81.
PMID: 9309700 [PubMed - indexed for MEDLINE]

505: Yatabe K, Kawai M.
Specific binding of Ulex europaeus agglutinin I lectin to sarcolemma of distal
myopathy with rimmed vacuole formation.
J Neurol. 1997 Aug;244(8):489-92.
PMID: 9309554 [PubMed - indexed for MEDLINE]

506: Prayson RA, Cohen ML.
Ubiquitin immunostaining and inclusion body myositis: study of 30 patients with
inclusion body myositis.
Hum Pathol. 1997 Aug;28(8):887-92.
PMID: 9269823 [PubMed - indexed for MEDLINE]

507: Amato AA, Barohn RJ.
Idiopathic inflammatory myopathies.
Neurol Clin. 1997 Aug;15(3):615-48. Review.
PMID: 9227956 [PubMed - indexed for MEDLINE]

508: Askanas V, McFerrin J, Alvarez RB, Baque S, Engel WK.
Beta APP gene transfer into cultured human muscle induces inclusion-body
myositis aspects.
Neuroreport. 1997 Jul 7;8(9-10):2155-8.
PMID: 9243602 [PubMed - indexed for MEDLINE]

509: Marchetti C, Bernasconi G, Reguzzoni M, Farina A.
The articular disc surface in different functional conditions of the human
temporo-mandibular joint.
J Oral Pathol Med. 1997 Jul;26(6):278-82.
PMID: 9234188 [PubMed - indexed for MEDLINE]

510: Behrens L, Bender A, Johnson MA, Hohlfeld R.
Cytotoxic mechanisms in inflammatory myopathies. Co-expression of Fas and
protective Bcl-2 in muscle fibres and inflammatory cells.
Brain. 1997 Jun;120 ( Pt 6):929-38.
PMID: 9217678 [PubMed - indexed for MEDLINE]

511: Mastaglia FL, Phillips BA, Zilko P.
Treatment of inflammatory myopathies.
Muscle Nerve. 1997 Jun;20(6):651-64. Review.
PMID: 9149071 [PubMed - indexed for MEDLINE]

512: Ono S, Takahashi K, Fukuoka Y, Jinnai K, Kanda F, Kurisaki H, Mitake S,
Inagaki T, Nagao K.
Intracytoplasmic inclusion bodies of the substantia nigra in myotonic
dystrophy. Immunohistochemical observations.
J Neurol Sci. 1997 May 29;148(2):193-8.
PMID: 9129116 [PubMed - indexed for MEDLINE]

513: Goebel HH, Anderson JR, Hubner C, Oexle K, Warlo I.
Congenital myopathy with excess of thin myofilaments.
Neuromuscul Disord. 1997 May;7(3):160-8.
PMID: 9185179 [PubMed - indexed for MEDLINE]

514: Mantegazza R, Bernasconi P, Confalonieri P, Cornelio F.
Inflammatory myopathies and systemic disorders: a review of immunopathogenetic
mechanisms and clinical features.
J Neurol. 1997 May;244(5):277-87. Review.
PMID: 9178151 [PubMed - indexed for MEDLINE]

515: Lundberg I, Ulfgren AK, Nyberg P, Andersson U, Klareskog L.
Cytokine production in muscle tissue of patients with idiopathic inflammatory
myopathies.
Arthritis Rheum. 1997 May;40(5):865-74.
PMID: 9153548 [PubMed - indexed for MEDLINE]

516: Authier FJ, Mhiri C, Chazaud B, Christov C, Cherin P, Barlovatz-Meimon G,
Gherardi RK.
Interleukin-1 expression in inflammatory myopathies: evidence of marked
immunoreactivity in sarcoid granulomas and muscle fibres showing ischaemic and
regenerative changes.
Neuropathol Appl Neurobiol. 1997 Apr;23(2):132-40.
PMID: 9160898 [PubMed - indexed for MEDLINE]

517: Sivakumar K, Semino-Mora C, Dalakas MC.
An inflammatory, familial, inclusion body myositis with autoimmune features and
a phenotype identical to sporadic inclusion body myositis. Studies in three
families.
Brain. 1997 Apr;120 ( Pt 4):653-61.
PMID: 9153127 [PubMed - indexed for MEDLINE]

518: Argov Z, Tiram E, Eisenberg I, Sadeh M, Seidman CE, Seidman JG, Karpati G,
Mitrani-Rosenbaum S.
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
Ann Neurol. 1997 Apr;41(4):548-51.
PMID: 9124813 [PubMed - indexed for MEDLINE]

519: Ikeuchi T, Asaka T, Saito M, Tanaka H, Higuchi S, Tanaka K, Saida K, Uyama
E, Mizusawa H, Fukuhara N, Nonaka I, Takamori M, Tsuji S.
Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to
chromosome 9.
Ann Neurol. 1997 Apr;41(4):432-7.
PMID: 9124799 [PubMed - indexed for MEDLINE]

520: Askanas V.
New developments in hereditary inclusion body myopathies.
Ann Neurol. 1997 Apr;41(4):421-2. No abstract available.
PMID: 9124797 [PubMed - indexed for MEDLINE]

521: Reichmann H, Goebel HH, Schneider C, Toyka KV.
Familial mixed congenital myopathy with rigid spine phenotype.
Muscle Nerve. 1997 Apr;20(4):411-7.
PMID: 9121497 [PubMed - indexed for MEDLINE]

522: Sekul EA, Chow C, Dalakas MC.
Magnetic resonance imaging of the forearm as a diagnostic aid in patients with
sporadic inclusion body myositis.
Neurology. 1997 Apr;48(4):863-6.
PMID: 9109868 [PubMed - indexed for MEDLINE]

523: Silva Oropeza E, Peralta Rosado HR, Valero Elizondo C, Sadowinski E,
Magana Serrano JA.
A case of amiodarone and neuromyopathy.
Rev Invest Clin. 1997 Mar-Apr;49(2):135-9.
PMID: 9294958 [PubMed - indexed for MEDLINE]

524: Jensen ML, Wieting JM, Andary MT, Fankhauser MJ, Jones MJ.
Inclusion body myositis and transitional cell carcinoma of the bladder:
significant resolution of symptoms after tumor excision.
Arch Phys Med Rehabil. 1997 Mar;78(3):327-9. Review.
PMID: 9084359 [PubMed - indexed for MEDLINE]

525: Dalakas MC, Sonies B, Dambrosia J, Sekul E, Cupler E, Sivakumar K.
Treatment of inclusion-body myositis with IVIg: a double-blind,
placebo-controlled study.
Neurology. 1997 Mar;48(3):712-6.
PMID: 9065553 [PubMed - indexed for MEDLINE]

526: Barohn RJ.
The therapeutic dilemma of inclusion body myositis.
Neurology. 1997 Mar;48(3):567-8. No abstract available.
PMID: 9065526 [PubMed - indexed for MEDLINE]

527: Sieb JP, VonOertzen J, Tolksdorf K, Dorfler P, Kappes-Horn K, Jerusalem F.

Sporadic adult-onset distal myopathy with rimmed vacuoles, 15-18 nm
tubulofilaments and extensive rod formation.
J Neurol Sci. 1997 Feb 27;146(1):81-4.
PMID: 9077500 [PubMed - indexed for MEDLINE]

528: Reed L, Young J, Goebel HH, Schochet SS Jr.
Congenital cytoplasmic body myopathy: case report.
J Child Neurol. 1997 Feb;12(2):149-52. No abstract available.
PMID: 9075028 [PubMed - indexed for MEDLINE]

529: Moslemi AR, Lindberg C, Oldfors A.
Analysis of multiple mitochondrial DNA deletions in inclusion body myositis.
Hum Mutat. 1997;10(5):381-6.
PMID: 9375854 [PubMed - indexed for MEDLINE]

530: Weitoft T.
Occurrence of polymyositis in the county of Gavleborg, Sweden.
Scand J Rheumatol. 1997;26(2):104-6.
PMID: 9137324 [PubMed - indexed for MEDLINE]

531: Blume G, Pestronk A, Frank B, Johns DR.
Polymyositis with cytochrome oxidase negative muscle fibres. Early quadriceps
weakness and poor response to immunosuppressive therapy.
Brain. 1997 Jan;120 ( Pt 1):39-45.
PMID: 9055796 [PubMed - indexed for MEDLINE]

532: Luciano CA, Dalakas MC.
Inclusion body myositis: no evidence for a neurogenic component.
Neurology. 1997 Jan;48(1):29-33.
PMID: 9008489 [PubMed - indexed for MEDLINE]

533: Dalakas MC, Illa I, Gallardo E, Juarez C.
Inclusion body myositis and paraproteinemia: incidence and immunopathologic
correlations.
Ann Neurol. 1997 Jan;41(1):100-4.
PMID: 9005871 [PubMed - indexed for MEDLINE]

534: Yang CC, Alvarez RB, Engel WK, Askanas V.
Increase of nitric oxide synthases and nitrotyrosine in inclusion-body
myositis.
Neuroreport. 1996 Dec 20;8(1):153-8.
PMID: 9051771 [PubMed - indexed for MEDLINE]

535: Serratrice G.
The three groups of polymyositis.
Rev Rhum Engl Ed. 1996 Dec;63(11):797-800. No abstract available.
PMID: 9010966 [PubMed - indexed for MEDLINE]

536: Cupler EJ, Leon-Monzon M, Miller J, Semino-Mora C, Anderson TL, Dalakas
MC.
Inclusion body myositis in HIV-1 and HTLV-1 infected patients.
Brain. 1996 Dec;119 ( Pt 6):1887-93.
PMID: 9009995 [PubMed - indexed for MEDLINE]

537: Mirabella M, Alvarez RB, Engel WK, Weisgraber KH, Askanas V.
Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body
myositis and myopathies.
Ann Neurol. 1996 Dec;40(6):864-72.
PMID: 9007091 [PubMed - indexed for MEDLINE]

538: Garlepp MJ, Mastaglia FL.
Apolipoprotein E and inclusion body myositis.
Ann Neurol. 1996 Dec;40(6):826-8. No abstract available.
PMID: 9007086 [PubMed - indexed for MEDLINE]

539: Basta M, Illa I, Dalakas MC.
Increased in vitro uptake of the complement C3b in the serum of patients with
Guillain-Barre syndrome, myasthenia gravis and dermatomyositis.
J Neuroimmunol. 1996 Dec;71(1-2):227-9.
PMID: 8982124 [PubMed - indexed for MEDLINE]

540: Schneider C, Gold R, Dalakas MC, Schmied M, Lassmann H, Toyka KV, Hartung
HP.
MHC class I-mediated cytotoxicity does not induce apoptosis in muscle fibers
nor in inflammatory T cells: studies in patients with polymyositis,
dermatomyositis, and inclusion body myositis.
J Neuropathol Exp Neurol. 1996 Dec;55(12):1205-9.
PMID: 8957443 [PubMed - indexed for MEDLINE]

541: Love S, Nicoll JA, Lowe J, Sherriff F.
Apolipoprotein E allele frequencies in sporadic inclusion body myositis.
Muscle Nerve. 1996 Dec;19(12):1605-7. No abstract available.
PMID: 8941276 [PubMed - indexed for MEDLINE]

542: Garlepp MJ.
Genetics of the idiopathic inflammatory myopathies.
Curr Opin Rheumatol. 1996 Nov;8(6):514-20. Review.
PMID: 9018454 [PubMed - indexed for MEDLINE]

543: Reimers CD, Schlotter B, Eicke BM, Witt TN.
Calf enlargement in neuromuscular diseases: a quantitative ultrasound study in
350 patients and review of the literature.
J Neurol Sci. 1996 Nov;143(1-2):46-56. Review.
PMID: 8981297 [PubMed - indexed for MEDLINE]

544: Rosenblum WI.
Two distinct forms of hyperphosphorylated tau in sporatic versus hereditary
inclusion myopathy.
J Neuropathol Exp Neurol. 1996 Nov;55(11):1179-80. No abstract available.
PMID: 8939201 [PubMed - indexed for MEDLINE]

545: Carpenter S.
Inclusion body myositis, a review.
J Neuropathol Exp Neurol. 1996 Nov;55(11):1105-14. Review. No abstract
available.
PMID: 8939193 [PubMed - indexed for MEDLINE]

546: Yamanishi Y, Maeda H, Katayama S, Ishioka S, Yamakido M.
Scleroderma-polymyositis overlap syndrome associated with anti-Ku antibody and
rimmed vacuole formation.
J Rheumatol. 1996 Nov;23(11):1991-4.
PMID: 8923381 [PubMed - indexed for MEDLINE]

547: Gentile S, Sacerdote I, Roccatello D, Giordana MT.
Progressive multifocal leukoencephalopathy during cyclosporine treatment. A
case report.
Ital J Neurol Sci. 1996 Oct;17(5):363-6. Review.
PMID: 8933230 [PubMed - indexed for MEDLINE]

548: Kagen LJ.
New developments in the myositis syndromes.
Bull Rheum Dis. 1996 Oct;45(6):1-4. Review. No abstract available.
PMID: 8885477 [PubMed - indexed for MEDLINE]

549: Amato AA, Gronseth GS, Jackson CE, Wolfe GI, Katz JS, Bryan WW, Barohn RJ.

Inclusion body myositis: clinical and pathological boundaries.
Ann Neurol. 1996 Oct;40(4):581-6.
PMID: 8871577 [PubMed - indexed for MEDLINE]

550: Sivakumar K, Dalakas MC.
The spectrum of familial inclusion body myopathies in 13 families and a
description of a quadriceps-sparing phenotype in non-Iranian Jews.
Neurology. 1996 Oct;47(4):977-84.
PMID: 8857730 [PubMed - indexed for MEDLINE]

551: Ono S, Takahashi K, Kanda F, Fukuoka Y, Jinnai K, Kurisaki H, Mitake S,
Inagaki T, Nagao K.
Immunohistochemical study of intracytoplasmic inclusion bodies of the thalamus
in myotonic dystrophy.
J Neurol Sci. 1996 Sep 1;140(1-2):96-100.
PMID: 8866433 [PubMed - indexed for MEDLINE]

552: Alexander JA, Huebner CJ.
Hepatitis C and inclusion body myositis.
Am J Gastroenterol. 1996 Sep;91(9):1845-7.
PMID: 8792712 [PubMed - indexed for MEDLINE]

553: Kumamoto T, Ueyama H, Fujimoto S, Nagao S, Tsuda T.
Clinicopathologic characteristics of polymyositis patients with numerous tissue
eosinophils.
Acta Neurol Scand. 1996 Aug;94(2):110-4.
PMID: 8891055 [PubMed - indexed for MEDLINE]

554: De Bleecker JL, Engel AG, Butcher EC.
Peripheral lymphoid tissue-like adhesion molecule expression in nodular
infiltrates in inflammatory myopathies.
Neuromuscul Disord. 1996 Aug;6(4):255-60.
PMID: 8887954 [PubMed - indexed for MEDLINE]

555: Park SH, Park HR.
Inclusion body myositis--a case report.
J Korean Med Sci. 1996 Aug;11(4):358-63.
PMID: 8878808 [PubMed - indexed for MEDLINE]

556: Askanas V, Engel WK, Mirabella M, Weisgraber KH, Saunders AM, Roses AD,
McFerrin J.
Apolipoprotein E alleles in sporadic inclusion-body myositis and hereditary
inclusion-body myopathy.
Ann Neurol. 1996 Aug;40(2):264-5. No abstract available.
PMID: 8773613 [PubMed - indexed for MEDLINE]

557: Mirabella M, Alvarez RB, Bilak M, Engel WK, Askanas V.
Difference in expression of phosphorylated tau epitopes between sporadic
inclusion-body myositis and hereditary inclusion-body myopathies.
J Neuropathol Exp Neurol. 1996 Jul;55(7):774-86.
PMID: 8965093 [PubMed - indexed for MEDLINE]

558: Cervernakova L, Sivakumar K, Nagle J, Dalakas MC, Goldfarb LG.
Is hereditary inclusion body myopathy a "familial prion disease" ?
Ann Neurol. 1996 Jul;40(1):128. No abstract available.
PMID: 8687183 [PubMed - indexed for MEDLINE]

559: Cid MC, Grau JM, Casademont J, Tobias E, Picazo A, Coll-Vinent B, Esparza
J, Pedrol E, Urbano-Marquez A.
Leucocyte/endothelial cell adhesion receptors in muscle biopsies from patients
with idiopathic inflammatory myopathies (IIM).
Clin Exp Immunol. 1996 Jun;104(3):467-73.
PMID: 9099932 [PubMed - indexed for MEDLINE]

560: [No authors listed]
Inflammatory disease.
Curr Opin Neurol. 1996 Jun;9(3):B65-76. No abstract available.
PMID: 8839622 [PubMed - indexed for MEDLINE]

561: Dalakas MC, Sivakumar K.
The immunopathologic and inflammatory differences between dermatomyositis,
polymyositis and sporadic inclusion body myositis.
Curr Opin Neurol. 1996 Jun;9(3):235-9. Review.
PMID: 8839618 [PubMed - indexed for MEDLINE]

562: Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC,
Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S.
Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a
study of 56 patients.
Ann Neurol. 1996 Jun;39(6):789-95.
PMID: 8651651 [PubMed - indexed for MEDLINE]

563: Felice KJ, Grunnet ML.
Inclusion body myositis associated with a severe unilateral levodopa-responsive
upper extremity tremor.
Muscle Nerve. 1996 Jun;19(6):787-9. No abstract available.
PMID: 8609934 [PubMed - indexed for MEDLINE]

564: Shapiro J, Martin S, DeGirolami U, Goyal R.
Inflammatory myopathy causing pharyngeal dysphagia: a new entity.
Ann Otol Rhinol Laryngol. 1996 May;105(5):331-5.
PMID: 8651624 [PubMed - indexed for MEDLINE]

565: Blumen SC, Sadeh M, Korczyn AD, Rouche A, Nisipeanu P, Asherov A, Tome FM.

Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara
Jews.
Neurology. 1996 May;46(5):1324-8.
PMID: 8628475 [PubMed - indexed for MEDLINE]

566: De Bleecker JL, Engel AG, Ertl BB.
Myofibrillar myopathy with abnormal foci of desmin positivity. II.
Immunocytochemical analysis reveals accumulation of multiple other proteins.
J Neuropathol Exp Neurol. 1996 May;55(5):563-77.
PMID: 8627347 [PubMed - indexed for MEDLINE]

567: Nakano S, Engel AG, Waclawik AJ, Emslie-Smith AM, Busis NA.
Myofibrillar myopathy with abnormal foci of desmin positivity. I. Light and
electron microscopy analysis of 10 cases.
J Neuropathol Exp Neurol. 1996 May;55(5):549-62.
PMID: 8627346 [PubMed - indexed for MEDLINE]

568: Dalakas MC.
Clinical benefits and immunopathological correlates of intravenous immune
globulin in the treatment of inflammatory myopathies.
Clin Exp Immunol. 1996 May;104 Suppl 1:55-60. Review.
PMID: 8625545 [PubMed - indexed for MEDLINE]

569: Garlepp MJ, Mastaglia FL.
Inclusion body myositis.
J Neurol Neurosurg Psychiatry. 1996 Mar;60(3):251-5. Review. No abstract
available.
PMID: 8609499 [PubMed - indexed for MEDLINE]

570: Askanas V, Alvarez RB, Mirabella M, Engel WK.
Use of anti-neurofilament antibody to identify paired-helical filaments in
inclusion-body myositis.
Ann Neurol. 1996 Mar;39(3):389-91.
PMID: 8602760 [PubMed - indexed for MEDLINE]

571: Naumann M, Reichmann H, Goebel HH, Moll C, Toyka KV.
Glucocorticoid-sensitive hereditary inclusion body myositis.
J Neurol. 1996 Feb;243(2):126-30.
PMID: 8750548 [PubMed - indexed for MEDLINE]

572: Mares M, Sartori MT, Casonato A, Melacini P, Angelini C, Girolami A.
Myopathy with tubular aggregates and hypertrophic cardiomyopathy in a patient
with type IIA von Willebrand disease.
Haematologia (Budap). 1996;27(4):201-8. No abstract available.
PMID: 14651221 [PubMed - indexed for MEDLINE]

573: Jongen PJ, Vingerhoets HM, Roeleveld K, Stegeman DF.
Automatic decomposition electromyography in idiopathic inflammatory myopathies.
J Neurol. 1996 Jan;243(1):79-85.
PMID: 8869392 [PubMed - indexed for MEDLINE]

574: Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, Seidman CE, Seidman JG.
Hereditary inclusion body myopathy maps to chromosome 9p1-q1.
Hum Mol Genet. 1996 Jan;5(1):159-163.
PMID: 8789455 [PubMed - indexed for MEDLINE]

575: Lloreta J, Roquer J, Corominas JM, Serrano S.
Hyperthyroid myopathy with mitochondrial paracrystalline rectangular
inclusions.
Ultrastruct Pathol. 1996 Jan-Feb;20(1):61-65.
PMID: 8789211 [PubMed - indexed for MEDLINE]

576: Chariot P, Ruet E, Authier FJ, Labes D, Poron F, Gherardi R.
Cytochrome c oxidase deficiencies in the muscle of patients with inflammatory
myopathies.
Acta Neuropathol (Berl). 1996;91(5):530-6.
PMID: 8740235 [PubMed - indexed for MEDLINE]

577: Schlesinger I, Soffer D, Lossos A, Meiner Z, Argov Z.
Inclusion body myositis: atypical clinical presentations.
Eur Neurol. 1996;36(2):89-93.
PMID: 8654492 [PubMed - indexed for MEDLINE]

578: Pruitt JN 2nd, Showalter CJ, Engel AG.
Sporadic inclusion body myositis: counts of different types of abnormal fibers.
Ann Neurol. 1996 Jan;39(1):139-43.
PMID: 8572661 [PubMed - indexed for MEDLINE]

579: Fyhr IM, Moslemi AR, Tarkowski A, Lindberg C, Oldfors A.
Limited T-cell receptor V gene usage in inclusion body myositis.
Scand J Immunol. 1996 Jan;43(1):109-14.
PMID: 8560189 [PubMed - indexed for MEDLINE]

580: Fox SA, Ward BK, Robbins PD, Mastaglia FL, Swanson NR.
Inclusion body myositis: investigation of the mumps virus hypothesis by
polymerase chain reaction.
Muscle Nerve. 1996 Jan;19(1):23-8.
PMID: 8538666 [PubMed - indexed for MEDLINE]

581: Lee CC, Huang CC, Chen SS.
Vacuolar changes in neuromuscular disorders: a morphometric study.
Zhonghua Yi Xue Za Zhi (Taipei). 1995 Dec;56(6):386-92.
PMID: 8851479 [PubMed - indexed for MEDLINE]

582: Lundberg I, Brengman JM, Engel AG.
Analysis of cytokine expression in muscle in inflammatory myopathies, Duchenne
dystrophy, and non-weak controls.
J Neuroimmunol. 1995 Dec;63(1):9-16.
PMID: 8557829 [PubMed - indexed for MEDLINE]

583: Garlepp MJ, Tabarias H, van Bockxmeer FM, Zilko PJ, Laing B, Mastaglia FL.

Apolipoprotein E epsilon 4 in inclusion body myositis.
Ann Neurol. 1995 Dec;38(6):957-9.
PMID: 8526471 [PubMed - indexed for MEDLINE]

584: Dalakas MC.
Update on the use of intravenous immune globulin in the treatment of patients
with inflammatory muscle disease.
J Clin Immunol. 1995 Nov;15(6 Suppl):70S-75S.
PMID: 8613495 [PubMed - indexed for MEDLINE]

585: Sussman GL, Pruzanski W.
Treatment of inflammatory myopathy with intravenous gamma globulin.
Curr Opin Rheumatol. 1995 Nov;7(6):510-5. Review.
PMID: 8579971 [PubMed - indexed for MEDLINE]

586: Askanas V, Engel WK.
New advances in the understanding of sporadic inclusion-body myositis and
hereditary inclusion-body myopathies.
Curr Opin Rheumatol. 1995 Nov;7(6):486-96. Review.
PMID: 8579968 [PubMed - indexed for MEDLINE]

587: Goebel HH.
Desmin-related neuromuscular disorders.
Muscle Nerve. 1995 Nov;18(11):1306-20. Review.
PMID: 7565929 [PubMed - indexed for MEDLINE]

588: Griggs RC, Askanas V, DiMauro S, Engel A, Karpati G, Mendell JR, Rowland
LP.
Inclusion body myositis and myopathies.
Ann Neurol. 1995 Nov;38(5):705-13. Review. No abstract available.
PMID: 7486861 [PubMed - indexed for MEDLINE]

589: Dasque F, Laroche M, Marque P, Le Vourc'h P, Moulinier L, Mazieres B,
Roques CF.
Isokinetic strength testing for evaluating the efficacy of intravenous immune
globulin therapy for inclusion body myositis.
Rev Rhum Engl Ed. 1995 Oct;62(9):598-601.
PMID: 8574634 [PubMed - indexed for MEDLINE]

590: Bergmann M, Kamarampaka M, Kuchelmeister K, Klein H, Koch H.
Nemaline myopathy: two autopsy reports.
Childs Nerv Syst. 1995 Oct;11(10):610-5.
PMID: 8556730 [PubMed - indexed for MEDLINE]

591: Di Rocco M, Callea F, Pollice B, Faraci M, Campiani F, Borrone C.
Arthrogryposis, renal dysfunction and cholestasis syndrome: report of five
patients from three Italian families.
Eur J Pediatr. 1995 Oct;154(10):835-9. Review.
PMID: 8529684 [PubMed - indexed for MEDLINE]

592: Nadkarni N, Freimer M, Mendell JR.
Amyloidosis causing a progressive myopathy.
Muscle Nerve. 1995 Sep;18(9):1016-8.
PMID: 7643863 [PubMed - indexed for MEDLINE]

593: Sivakumar K, Cervenakova L, Dalakas MC, Leon-Monzon M, Isaacson SH, Nagle
JW, Vasconcelos O, Goldfarb LG.
Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion
body myopathy.
Ann Neurol. 1995 Aug;38(2):267-9.
PMID: 7654077 [PubMed - indexed for MEDLINE]

594: Oddis CV, Medsger TA Jr.
Inflammatory myopathies.
Baillieres Clin Rheumatol. 1995 Aug;9(3):497-514. Review.
PMID: 7497535 [PubMed - indexed for MEDLINE]

595: Sherriff FE, Joachim CL, Squier MV, Esiri MM.
Ubiquitinated inclusions in inclusion-body myositis patients are immunoreactive
for cathepsin D but not beta-amyloid.
Neurosci Lett. 1995 Jul 14;194(1-2):37-40.
PMID: 7478207 [PubMed - indexed for MEDLINE]

596: Barohn RJ, Amato AA, Sahenk Z, Kissel JT, Mendell JR.
Inclusion body myositis: explanation for poor response to immunosuppressive
therapy.
Neurology. 1995 Jul;45(7):1302-4. Erratum in: Neurology 1995 Dec;45(12):2304.
PMID: 7617187 [PubMed - indexed for MEDLINE]

597: Oldfors A, Moslemi AR, Fyhr IM, Holme E, Larsson NG, Lindberg C.
Mitochondrial DNA deletions in muscle fibers in inclusion body myositis.
J Neuropathol Exp Neurol. 1995 Jul;54(4):581-7.
PMID: 7602331 [PubMed - indexed for MEDLINE]

598: Dalakas MC, Illa I.
Common variable immunodeficiency and inclusion body myositis: a distinct
myopathy mediated by natural killer cells.
Ann Neurol. 1995 Jun;37(6):806-10.
PMID: 7778855 [PubMed - indexed for MEDLINE]

599: O'Hanlon TP, Messersmith WA, Dalakas MC, Plotz PH, Miller FW.
Gamma delta T cell receptor gene expression by muscle-infiltrating lymphocytes
in the idiopathic inflammatory myopathies.
Clin Exp Immunol. 1995 Jun;100(3):519-28.
PMID: 7774065 [PubMed - indexed for MEDLINE]

600: De Bleecker JL, Engel AG.
Immunocytochemical study of CD45 T cell isoforms in inflammatory myopathies.
Am J Pathol. 1995 May;146(5):1178-87.
PMID: 7747812 [PubMed - indexed for MEDLINE]

601: Hund E, Heckl R, Goebel HH, Meinck HM.
Inclusion body myositis presenting with isolated erector spinae paresis.
Neurology. 1995 May;45(5):993-4.
PMID: 7746422 [PubMed - indexed for MEDLINE]

602: Neufeld MY, Sadeh M, Assa B, Kushnir M, Korczyn AD.
Phenotypic heterogeneity in familial inclusion body myopathy.
Muscle Nerve. 1995 May;18(5):546-8. No abstract available.
PMID: 7739644 [PubMed - indexed for MEDLINE]

603: Lindberg C, Oldfors A, Tarkowski A.
Local T-cell proliferation and differentiation in inflammatory myopathies.
Scand J Immunol. 1995 May;41(5):421-6.
PMID: 7725060 [PubMed - indexed for MEDLINE]

604: Brais B, Xie YG, Sanson M, Morgan K, Weissenbach J, Korczyn AD, Blumen SC,
Fardeau M, Tome FM, Bouchard JP, et al.
The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac
alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13.
Hum Mol Genet. 1995 Mar;4(3):429-34.
PMID: 7795598 [PubMed - indexed for MEDLINE]

605: Jongen PJ, ter Laak HJ, Van de Putte LB.
Inclusion body myositis responding to longterm chlorambucil treatment.
J Rheumatol. 1995 Mar;22(3):576-8. No abstract available.
PMID: 7783093 [PubMed - indexed for MEDLINE]

606: Wallgren-Pettersson C, Jasani B, Newman GR, Morris GE, Jones S, Singhrao
S, Clarke A, Virtanen I, Holmberg C, Rapola J.
Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological
confirmation by light and electron microscopy.
Neuromuscul Disord. 1995 Mar;5(2):93-104.
PMID: 7767098 [PubMed - indexed for MEDLINE]

607: Schroder JM, Krabbe B, Weis J.
Oculopharyngeal muscular dystrophy: clinical and morphological follow-up study
reveals mitochondrial alterations and unique nuclear inclusions in a severe
autosomal recessive type.
Neuropathol Appl Neurobiol. 1995 Feb;21(1):68-73.
PMID: 7770123 [PubMed - indexed for MEDLINE]

608: Adams EM, Plotz PH.
The treatment of myositis. How to approach resistant disease.
Rheum Dis Clin North Am. 1995 Feb;21(1):179-202. Review.
PMID: 7732167 [PubMed - indexed for MEDLINE]

609: Harrington CR, Anderson JR, Chan KK.
Apolipoprotein E type epsilon 4 allele frequency is not increased in patients
with sporadic inclusion-body myositis.
Neurosci Lett. 1995 Jan 2;183(1-2):35-8.
PMID: 7746481 [PubMed - indexed for MEDLINE]

610: Murakami N, Ishiguro K, Ihara Y, Nonaka I, Sugita H, Imahori K.
Tau protein immunoreactivity in muscle fibers with rimmed vacuoles differs from
that in regenerating muscle fibers.
Acta Neuropathol (Berl). 1995;90(5):467-71.
PMID: 8560979 [PubMed - indexed for MEDLINE]

611: Rifai Z, Welle S, Kamp C, Thornton CA.
Ragged red fibers in normal aging and inflammatory myopathy.
Ann Neurol. 1995 Jan;37(1):24-9.
PMID: 7818253 [PubMed - indexed for MEDLINE]

612: Kiyomoto BH, Murakami N, Kobayashi Y, Nihei K, Tanaka T, Takeshita K,
Nonaka I.
Fatal reducing body myopathy. Ultrastructural and immunohistochemical
observations.
J Neurol Sci. 1995 Jan;128(1):58-65.
PMID: 7722535 [PubMed - indexed for MEDLINE]

613: Jongen PJ, Ter Laak HJ, Stadhouders AM.
Rimmed basophilic vacuoles and filamentous inclusions in neuromuscular
disorders.
Neuromuscul Disord. 1995 Jan;5(1):31-8.
PMID: 7719139 [PubMed - indexed for MEDLINE]

614: Murakami N, Ihara Y, Nonaka I.
Muscle fiber degeneration in distal myopathy with rimmed vacuole formation.
Acta Neuropathol (Berl). 1995;89(1):29-34.
PMID: 7709728 [PubMed - indexed for MEDLINE]

615: Kiyomoto BH, Murakami N, Kishibayashi J, Sunohara N, Nonaka I.
Reducing bodies in distal myopathy with rimmed vacuole formation.
Acta Neuropathol (Berl). 1995;89(1):109-11.
PMID: 7709723 [PubMed - indexed for MEDLINE]

616: Sarkozi E, Askanas V, Engel WK.
Abnormal accumulation of prion protein mRNA in muscle fibers of patients with
sporadic inclusion-body myositis and hereditary inclusion-body myopathy.
Am J Pathol. 1994 Dec;145(6):1280-4.
PMID: 7992832 [PubMed - indexed for MEDLINE]

617: Lindberg C, Oldfors A, Tarkowski A.
Restricted use of T cell receptor V genes in endomysial infiltrates of patients
with inflammatory myopathies.
Eur J Immunol. 1994 Nov;24(11):2659-63.
PMID: 7957558 [PubMed - indexed for MEDLINE]

618: Liou CW, Huang CC, Chee EC, Jong YJ, Tsai JL, Pang CY, Lee HC, Wei YH.
MELAS syndrome: correlation between clinical features and molecular genetic
analysis.
Acta Neurol Scand. 1994 Nov;90(5):354-9.
PMID: 7887136 [PubMed - indexed for MEDLINE]

619: Dalakas MC.
Current treatment of the inflammatory myopathies.
Curr Opin Rheumatol. 1994 Nov;6(6):595-601. Review.
PMID: 7865379 [PubMed - indexed for MEDLINE]

620: Mantegazza R, Bernasconi P.
Cellular aspects of myositis.
Curr Opin Rheumatol. 1994 Nov;6(6):568-74. Review.
PMID: 7865375 [PubMed - indexed for MEDLINE]

621: Calabrese LH, Chou SM.
Inclusion body myositis.
Rheum Dis Clin North Am. 1994 Nov;20(4):955-72. Review.
PMID: 7855331 [PubMed - indexed for MEDLINE]

622: Callen JP.
Relationship of cancer to inflammatory muscle diseases. Dermatomyositis,
polymyositis, and inclusion body myositis.
Rheum Dis Clin North Am. 1994 Nov;20(4):943-53. Review.
PMID: 7855330 [PubMed - indexed for MEDLINE]

623: Miller FW.
Classification and prognosis of inflammatory muscle disease.
Rheum Dis Clin North Am. 1994 Nov;20(4):811-26. Review.
PMID: 7855323 [PubMed - indexed for MEDLINE]

624: Garlepp MJ, Laing B, Zilko PJ, Ollier W, Mastaglia FL.
HLA associations with inclusion body myositis.
Clin Exp Immunol. 1994 Oct;98(1):40-5.
PMID: 7923882 [PubMed - indexed for MEDLINE]

625: Askanas V, Engel WK, Mirabella M.
Idiopathic inflammatory myopathies: inclusion-body myositis, polymyositis, and
dermatomyositis.
Curr Opin Neurol. 1994 Oct;7(5):448-56. Review.
PMID: 7804466 [PubMed - indexed for MEDLINE]

626: Barohn RJ, Jackson CE, Kagan-Hallet KS.
Neonatal nemaline myopathy with abundant intranuclear rods.
Neuromuscul Disord. 1994 Sep-Nov;4(5-6):513-20.
PMID: 7881297 [PubMed - indexed for MEDLINE]

627: Amato AA, Barohn RJ, Jackson CE, Pappert EJ, Sahenk Z, Kissel JT.
Inclusion body myositis: treatment with intravenous immunoglobulin.
Neurology. 1994 Aug;44(8):1516-8.
PMID: 8058161 [PubMed - indexed for MEDLINE]

628: De Bleecker JL, Engel AG.
Expression of cell adhesion molecules in inflammatory myopathies and Duchenne
dystrophy.
J Neuropathol Exp Neurol. 1994 Jul;53(4):369-76.
PMID: 8021710 [PubMed - indexed for MEDLINE]

629: Helliwell TR, Green AR, Green A, Edwards RH.
Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions
containing desmin, dystrophin and vimentin.
J Neurol Sci. 1994 Jul;124(2):174-87.
PMID: 7964869 [PubMed - indexed for MEDLINE]

630: Hilton DA, Fletcher A, Pringle JH.
Absence of Coxsackie viruses in idiopathic inflammatory muscle disease by in
situ hybridization.
Neuropathol Appl Neurobiol. 1994 Jun;20(3):238-42.
PMID: 7936073 [PubMed - indexed for MEDLINE]

631: O'Hanlon TP, Dalakas MC, Plotz PH, Miller FW.
The alpha beta T-cell receptor repertoire in inclusion body myositis: diverse
patterns of gene expression by muscle-infiltrating lymphocytes.
J Autoimmun. 1994 Jun;7(3):321-33.
PMID: 7916906 [PubMed - indexed for MEDLINE]

632: Stadhouders AM, Jap PH, Winkler HP, Eppenberger HM, Wallimann T.
Mitochondrial creatine kinase: a major constituent of pathological inclusions
seen in mitochondrial myopathies.
Proc Natl Acad Sci U S A. 1994 May 24;91(11):5089-93.
PMID: 8197190 [PubMed - indexed for MEDLINE]

633: Nalbantoglu J, Karpati G, Carpenter S.
Conspicuous accumulation of a single-stranded DNA binding protein in skeletal
muscle fibers in inclusion body myositis.
Am J Pathol. 1994 May;144(5):874-82.
PMID: 8178939 [PubMed - indexed for MEDLINE]

634: Oyanagi K, Ogawa H, Nakajima T.
Rod-like intracytoplasmic inclusions in large neurons of the caudate nucleus:
frequent appearance in myotonic dystrophy.
Clin Neuropathol. 1994 May-Jun;13(3):134-8.
PMID: 8088033 [PubMed - indexed for MEDLINE]

635: Orimo S, Koga R, Goto K, Nakamura K, Arai M, Tamaki M, Sugita H, Nonaka I,
Arahata K.
Immunohistochemical analysis of perforin and granzyme A in inflammatory
myopathies.
Neuromuscul Disord. 1994 May;4(3):219-26.
PMID: 7919969 [PubMed - indexed for MEDLINE]

636: Wyss M, Wallimann T.
Creatine metabolism and the consequences of creatine depletion in muscle.
Mol Cell Biochem. 1994 Apr-May;133-134:51-66. Review.
PMID: 7808465 [PubMed - indexed for MEDLINE]

637: Reimers CD, Schedel H, Fleckenstein JL, Nagele M, Witt TN, Pongratz DE,
Vogl TJ.
Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory
myopathies of adults.
J Neurol. 1994 Mar;241(5):306-14.
PMID: 8006684 [PubMed - indexed for MEDLINE]

638: Askanas V, Mirabella M, Engel WK, Alvarez RB, Weisgraber KH.
Apolipoprotein E immunoreactive deposits in inclusion-body muscle diseases.
Lancet. 1994 Feb 5;343(8893):364-5. No abstract available.
PMID: 7905181 [PubMed - indexed for MEDLINE]

639: Lindberg C, Persson LI, Bjorkander J, Oldfors A.
Inclusion body myositis: clinical, morphological, physiological and laboratory
findings in 18 cases.
Acta Neurol Scand. 1994 Feb;89(2):123-31.
PMID: 8191875 [PubMed - indexed for MEDLINE]

640: Soden M, Boundy K, Burrow D, Blumbergs P, Ahern M.
Inclusion body myositis in association with rheumatoid arthritis.
J Rheumatol. 1994 Feb;21(2):344-6.
PMID: 8182647 [PubMed - indexed for MEDLINE]

641: Askanas V, Engel WK, Bilak M, Alvarez RB, Selkoe DJ.
Twisted tubulofilaments of inclusion body myositis muscle resemble paired
helical filaments of Alzheimer brain and contain hyperphosphorylated tau.
Am J Pathol. 1994 Jan;144(1):177-87.
PMID: 8291607 [PubMed - indexed for MEDLINE]

642: Jamroz E, Marszal E, Glinka Z, Fidzianska A.
Ultrastructure of peripheral blood lymphocytes in some degenerative central
nervous system disease.
Folia Neuropathol. 1994;32(2):81-6.
PMID: 7922111 [PubMed - indexed for MEDLINE]

643: Bartoccioni E, Gallucci S, Scuderi F, Ricci E, Servidei S, Broccolini A,
Tonali P.
MHC class I, MHC class II and intercellular adhesion molecule-1 (ICAM-1)
expression in inflammatory myopathies.
Clin Exp Immunol. 1994 Jan;95(1):166-72.
PMID: 7507012 [PubMed - indexed for MEDLINE]

644: DeArmond SJ.
Alzheimer's disease and Creutzfeldt-Jakob disease: overlap of pathogenic
mechanisms.
Curr Opin Neurol. 1993 Dec;6(6):872-81. Review.
PMID: 7904883 [PubMed - indexed for MEDLINE]

645: Rifai Z, Kazee AM, Kamp C, Griggs RC.
Intranuclear rods in severe congenital nemaline myopathy.
Neurology. 1993 Nov;43(11):2372-7.
PMID: 8232959 [PubMed - indexed for MEDLINE]

646: Mastaglia FL, Laing BA, Zilko P.
Treatment of inflammatory myopathies.
Baillieres Clin Neurol. 1993 Nov;2(3):717-40. Review.
PMID: 8156149 [PubMed - indexed for MEDLINE]

647: Hohlfeld R, Goebels N, Engel AG.
Cellular mechanisms in inflammatory myopathies.
Baillieres Clin Neurol. 1993 Nov;2(3):617-35. Review.
PMID: 8156145 [PubMed - indexed for MEDLINE]

648: Garlepp MJ.
Immunogenetics of inflammatory myopathies.
Baillieres Clin Neurol. 1993 Nov;2(3):579-97. Review.
PMID: 8156144 [PubMed - indexed for MEDLINE]

649: Chou SM.
Inclusion body myositis.
Baillieres Clin Neurol. 1993 Nov;2(3):557-77. Review.
PMID: 8156143 [PubMed - indexed for MEDLINE]

650: Askanas V, Engel WK.
New advances in inclusion-body myositis.
Curr Opin Rheumatol. 1993 Nov;5(6):732-41. Review.
PMID: 8117535 [PubMed - indexed for MEDLINE]

651: Askanas V, Bilak M, Engel WK, Alvarez RB, Tome F, Leclerc A.
Prion protein is abnormally accumulated in inclusion-body myositis.
Neuroreport. 1993 Oct 25;5(1):25-8.
PMID: 8280854 [PubMed - indexed for MEDLINE]

652: Lane RJ, McLean KA, Moss J, Woodrow DF.
Myopathy in HIV infection: the role of zidovudine and the significance of
tubuloreticular inclusions.
Neuropathol Appl Neurobiol. 1993 Oct;19(5):406-13.
PMID: 8278024 [PubMed - indexed for MEDLINE]

653: Askanas V, Alvarez RB, Engel WK.
beta-Amyloid precursor epitopes in muscle fibers of inclusion body myositis.
Ann Neurol. 1993 Oct;34(4):551-60.
PMID: 7692809 [PubMed - indexed for MEDLINE]

654: Cohen R, Lipper S, Dantzker DR.
Inclusion body myositis as a cause of respiratory failure.
Chest. 1993 Sep;104(3):975-7.
PMID: 8396004 [PubMed - indexed for MEDLINE]

655: Sekul EA, Dalakas MC.
Inclusion body myositis: new concepts.
Semin Neurol. 1993 Sep;13(3):256-63. Review. No abstract available.
PMID: 8272596 [PubMed - indexed for MEDLINE]

656: Lohr HF, Bocher WO, Hermann E, Muller-Quernheim J, Schwickert H, Meyer zum
Buschenfelde KH, Gerken G.
Interstitial alveolitis as early manifestation of anti-Jo-1 positive
polymyositis.
Z Rheumatol. 1993 Sep-Oct;52(5):307-11.
PMID: 8259723 [PubMed - indexed for MEDLINE]

657: Caron A, Chapon F, Berthelin C, Viader F, Lechevalier B.
Inclusions in familial cytoplasmic body myopathy are stained by anti-dystrophin
antibodies.
Neuromuscul Disord. 1993 Sep-Nov;3(5-6):541-6.
PMID: 8186708 [PubMed - indexed for MEDLINE]

658: Albrecht S, Bilbao JM.
Ubiquitin expression in inclusion body myositis. An immunohistochemical study.
Arch Pathol Lab Med. 1993 Aug;117(8):789-93.
PMID: 8393651 [PubMed - indexed for MEDLINE]

659: Salvarani C, Boiardi L, Maldini MC, Mancini R, Rinaldi M, Macchioni P,
Portioli I.
High dose immunoglobulin therapy in a case of inclusion body myositis: clinical
and immunologic aspects.
J Rheumatol. 1993 Aug;20(8):1455-6. No abstract available.
PMID: 8230050 [PubMed - indexed for MEDLINE]

660: Kunze D, Rustow B.
Pathobiochemical aspects of cytoskeleton components.
Eur J Clin Chem Clin Biochem. 1993 Aug;31(8):477-89. Review.
PMID: 8218579 [PubMed - indexed for MEDLINE]

661: Abe K, Kobayashi K, Chida K, Kimura N, Kogure K.
Dominantly inherited cytoplasmic body myopathy in a Japanese kindred.
Tohoku J Exp Med. 1993 Aug;170(4):261-72.
PMID: 8122252 [PubMed - indexed for MEDLINE]

662: Leff RL, Miller FW, Hicks J, Fraser DD, Plotz PH.
The treatment of inclusion body myositis: a retrospective review and a
randomized, prospective trial of immunosuppressive therapy.
Medicine (Baltimore). 1993 Jul;72(4):225-35.
PMID: 8393509 [PubMed - indexed for MEDLINE]

663: Leclerc A, Tome FM, Fardeau M.
Ubiquitin and beta-amyloid-protein in inclusion body myositis (IBM), familial
IBM-like disorder and oculopharyngeal muscular dystrophy: an immunocytochemical
study.
Neuromuscul Disord. 1993 Jul;3(4):283-91.
PMID: 8268725 [PubMed - indexed for MEDLINE]

664: Sarkozi E, Askanas V, Johnson SA, Engel WK, Alvarez RB.
beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis
muscle.
Neuroreport. 1993 Jun;4(6):815-8.
PMID: 8394158 [PubMed - indexed for MEDLINE]

665: Askanas V, Engel WK, Alvarez RB.
Enhanced detection of congo-red-positive amyloid deposits in muscle fibers of
inclusion body myositis and brain of Alzheimer's disease using fluorescence
technique.
Neurology. 1993 Jun;43(6):1265-7. No abstract available.
PMID: 8170582 [PubMed - indexed for MEDLINE]

666: Riminton DS, Chambers ST, Parkin PJ, Pollock M, Donaldson IM.
Inclusion body myositis presenting solely as dysphagia.
Neurology. 1993 Jun;43(6):1241-3.
PMID: 8170574 [PubMed - indexed for MEDLINE]

667: Reimers CD, Fleckenstein JL, Witt TN, Muller-Felber W, Pongratz DE.
Muscular ultrasound in idiopathic inflammatory myopathies of adults.
J Neurol Sci. 1993 May;116(1):82-92.
PMID: 8509807 [PubMed - indexed for MEDLINE]

668: Soueidan SA, Dalakas MC.
Treatment of inclusion-body myositis with high-dose intravenous immunoglobulin.
Neurology. 1993 May;43(5):876-9.
PMID: 8492940 [PubMed - indexed for MEDLINE]

669: Palmucci L, Doriguzzi C, Mongini T, Chiado-Piat L.
Adult onset nemaline myopathy: a distinct nosologic entity?
Clin Neuropathol. 1993 May-Jun;12(3):153-5.
PMID: 8391957 [PubMed - indexed for MEDLINE]

670: Beyenburg S, Zierz S, Jerusalem F.
Inclusion body myositis: clinical and histopathological features of 36
patients.
Clin Investig. 1993 May;71(5):351-61.
PMID: 8389626 [PubMed - indexed for MEDLINE]

671: Fogel SP, DeTar MW, Shimada H, Chandrasoma PT.
Sporadic visceral myopathy with inclusion bodies. A light-microscopic and
ultrastructural study.
Am J Surg Pathol. 1993 May;17(5):473-81.
PMID: 8385883 [PubMed - indexed for MEDLINE]

672: Joffe MM, Love LA, Leff RL, Fraser DD, Targoff IN, Hicks JE, Plotz PH,
Miller FW.
Drug therapy of the idiopathic inflammatory myopathies: predictors of response
to prednisone, azathioprine, and methotrexate and a comparison of their
efficacy.
Am J Med. 1993 Apr;94(4):379-87.
PMID: 8386437 [PubMed - indexed for MEDLINE]

673: Oldfors A, Larsson NG, Lindberg C, Holme E.
Mitochondrial DNA deletions in inclusion body myositis.
Brain. 1993 Apr;116 ( Pt 2):325-36.
PMID: 8384916 [PubMed - indexed for MEDLINE]

674: Ytterberg SR, Roelofs RI, Mahowald ML.
Inclusion body myositis and renal cell carcinoma. Report of two cases and
review of the literature.
Arthritis Rheum. 1993 Mar;36(3):416-21. Review.
PMID: 8383972 [PubMed - indexed for MEDLINE]

675: Borg K, Ahlberg G, Hedberg B, Edstrom L.
Muscle fibre degeneration in distal myopathy (Welander)--ultrastructure related
to immunohistochemical observations on cytoskeletal proteins and Leu-19 antigen.
Neuromuscul Disord. 1993 Mar;3(2):149-55.
PMID: 7689381 [PubMed - indexed for MEDLINE]

676: Ceuterick C, Martin JJ, Martens C.
Hyaline bodies in skeletal muscle of a patient with a mild chronic
nonprogressive congenital myopathy.
Clin Neuropathol. 1993 Mar-Apr;12(2):79-83.
PMID: 7682901 [PubMed - indexed for MEDLINE]

677: Villanova M, Kawai M, Lubke U, Oh SJ, Perry G, Six J, Ceuterick C, Martin
JJ, Cras P.
Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular
dystrophy contain amyloid precursor protein and lysosomal markers.
Brain Res. 1993 Feb 19;603(2):343-7.
PMID: 8461987 [PubMed - indexed for MEDLINE]

678: Hopkinson ND, Hunt C, Powell RJ, Lowe J.
Inclusion body myositis: an underdiagnosed condition?
Ann Rheum Dis. 1993 Feb;52(2):147-51.
PMID: 8383483 [PubMed - indexed for MEDLINE]

679: Bilak M, Askanas V, Engel WK.
Strong immunoreactivity of alpha 1-antichymotrypsin co-localizes with
beta-amyloid protein and ubiquitin in vacuolated muscle fibers of inclusion-body
myositis.
Acta Neuropathol (Berl). 1993;85(4):378-82.
PMID: 8386897 [PubMed - indexed for MEDLINE]

680: Nicoll JA, Moss TH, Love S, Campbell MJ, Schutt WH.
Clinical and autopsy findings in two cases of MELAS presenting with stroke-like
episodes but without clinical myopathy.
Clin Neuropathol. 1993 Jan-Feb;12(1):38-43.
PMID: 8382573 [PubMed - indexed for MEDLINE]

681: Kalovidouris AE.
Immune aspects of myositis.
Curr Opin Rheumatol. 1992 Dec;4(6):809-14. Review.
PMID: 1333783 [PubMed - indexed for MEDLINE]

682: Averbuch-Heller L, Steiner I, Abramsky O.
Neurologic manifestations of progressive systemic sclerosis.
Arch Neurol. 1992 Dec;49(12):1292-5.
PMID: 1333182 [PubMed - indexed for MEDLINE]

683: Mendell JR, Sahenk Z.
Inclusion body myositis.
Neurology. 1992 Nov;42(11):2231-2. No abstract available.
PMID: 1279467 [PubMed - indexed for MEDLINE]

684: Dalakas MC.
Clinical, immunopathologic, and therapeutic considerations of inflammatory
myopathies.
Clin Neuropharmacol. 1992 Oct;15(5):327-51. Review.
PMID: 1423335 [PubMed - indexed for MEDLINE]

685: Verma A, Bradley WG, Soule NW, Pendlebury WW, Kelly J, Adelman LS, Chou
SM, Karpati G, Brenner JF.
Quantitative morphometric study of muscle in inclusion body myositis.
J Neurol Sci. 1992 Oct;112(1-2):192-8.
PMID: 1335036 [PubMed - indexed for MEDLINE]

686: Isaacs H, Badenhorst ME.
Internalised capillaries, neuromyopathy and myalgia.
J Neurol Neurosurg Psychiatry. 1992 Oct;55(10):921-4.
PMID: 1331336 [PubMed - indexed for MEDLINE]

687: Dalakas MC.
Inflammatory and toxic myopathies.
Curr Opin Neurol Neurosurg. 1992 Oct;5(5):645-54. Review.
PMID: 1327303 [PubMed - indexed for MEDLINE]

688: Sayers ME, Chou SM, Calabrese LH.
Inclusion body myositis: analysis of 32 cases.
J Rheumatol. 1992 Sep;19(9):1385-9.
PMID: 1331441 [PubMed - indexed for MEDLINE]

689: Wortmann RL.
The dilemma of treating patients with inclusion body myositis.
J Rheumatol. 1992 Sep;19(9):1327-9. No abstract available.
PMID: 1331440 [PubMed - indexed for MEDLINE]

690: Leon-Monzon M, Dalakas MC.
Absence of persistent infection with enteroviruses in muscles of patients with
inflammatory myopathies.
Ann Neurol. 1992 Aug;32(2):219-22.
PMID: 1324633 [PubMed - indexed for MEDLINE]

691: Askanas V, Engel WK, Alvarez RB.
Light and electron microscopic localization of beta-amyloid protein in muscle
biopsies of patients with inclusion-body myositis.
Am J Pathol. 1992 Jul;141(1):31-6.
PMID: 1321564 [PubMed - indexed for MEDLINE]

692: Lindal S, Lund I, Torbergsen T, Aasly J, Mellgren SI, Borud O, Monstad P.
Mitochondrial diseases and myopathies: a series of muscle biopsy specimens with
ultrastructural changes in the mitochondria.
Ultrastruct Pathol. 1992 May-Jun;16(3):263-75.
PMID: 1316655 [PubMed - indexed for MEDLINE]

693: Dwyer BA, Mayer RF, Lee SC.
Progressive nemaline (rod) myopathy as a presentation of human immunodeficiency
virus infection.
Arch Neurol. 1992 May;49(5):440. No abstract available.
PMID: 1316119 [PubMed - indexed for MEDLINE]

694: Neville HE, Baumbach LL, Ringel SP, Russo LS Jr, Sujansky E, Garcia CA.
Familial inclusion body myositis: evidence for autosomal dominant inheritance.
Neurology. 1992 Apr;42(4):897-902.
PMID: 1314344 [PubMed - indexed for MEDLINE]

695: Iannaccone ST.
Myogenes and myotubes.
J Child Neurol. 1992 Apr;7(2):180-7. Review.
PMID: 1315354 [PubMed - indexed for MEDLINE]

696: Nomizu S, Person DA, Saito C, Lockett LJ.
A unique case of reducing body myopathy.
Muscle Nerve. 1992 Apr;15(4):463-6.
PMID: 1314327 [PubMed - indexed for MEDLINE]

697: Darrow DH, Hoffman HT, Barnes GJ, Wiley CA.
Management of dysphagia in inclusion body myositis.
Arch Otolaryngol Head Neck Surg. 1992 Mar;118(3):313-7. Review.
PMID: 1313247 [PubMed - indexed for MEDLINE]

698: Reece RL, Scott PC, Barr DA.
Some unusual diseases in the birds of Victoria, Australia.
Vet Rec. 1992 Feb 29;130(9):178-85.
PMID: 1566552 [PubMed - indexed for MEDLINE]

699: Askanas V, Engel WK, Alvarez RB, Glenner GG.
beta-Amyloid protein immunoreactivity in muscle of patients with inclusion-body
myositis.
Lancet. 1992 Feb 29;339(8792):560-1. No abstract available.
PMID: 1346915 [PubMed - indexed for MEDLINE]

700: Khraishi MM, Jay V, Keystone EC.
Inclusion body myositis in association with vitamin B12 deficiency and
Sjogren's syndrome.
J Rheumatol. 1992 Feb;19(2):306-9.
PMID: 1629834 [PubMed - indexed for MEDLINE]

701: Askanas V, Serdaroglu P, Engel WK, Alvarez RB.
Immunocytochemical localization of ubiquitin in inclusion body myositis allows
its light-microscopic distinction from polymyositis.
Neurology. 1992 Feb;42(2):460-1. No abstract available.
PMID: 1310532 [PubMed - indexed for MEDLINE]

702: Hohlfeld R, Engel AG.
The role of gamma-delta T lymphocytes in inflammatory muscle disease.
Chem Immunol. 1992;53:75-85. Review.
PMID: 1534237 [PubMed - indexed for MEDLINE]

703: Carpenter S, Karpati G.
The pathological diagnosis of specific inflammatory myopathies.
Brain Pathol. 1992 Jan;2(1):13-9. Review.
PMID: 1341942 [PubMed - indexed for MEDLINE]

704: Fidzianska A, Drac H, Glinka Z.
Inclusion body myositis (IBM). Morphological study.
Neuropatol Pol. 1992;30(3-4):199-207.
PMID: 1340913 [PubMed - indexed for MEDLINE]

705: Jay V, Christodoulou J, Mercer-Connolly A, McInnes RR.
"Reducing body"-like inclusions in skeletal muscle in childhood-onset acid
maltase deficiency.
Acta Neuropathol (Berl). 1992;85(1):111-5.
PMID: 1337420 [PubMed - indexed for MEDLINE]

706: Del Bigio MR, Jay V.
Inclusion body myositis with abundant ring fibers.
Acta Neuropathol (Berl). 1992;85(1):105-10.
PMID: 1337419 [PubMed - indexed for MEDLINE]

707: Askanas V, Alvarez RB.
Fast and reliable new method for electron-microscopic identification of
cytoplasmic tubulo-filaments in muscle biopsies of patients with inclusion-body
myositis.
Acta Neuropathol (Berl). 1992;84(3):335-6. No abstract available.
PMID: 1329431 [PubMed - indexed for MEDLINE]

708: Maat-Schieman ML, Macfarlane JD, Bots GT, Wintzen AR.
Inclusion body myositis: its relative frequency in elderly people.
Clin Neurol Neurosurg. 1992;94 Suppl:S118-20.
PMID: 1320483 [PubMed - indexed for MEDLINE]

709: Goebel HH, Shin YS, Gullotta F, Yokota T, Alroy J, Voit T, Haller P,
Schulz A.
Adult polyglucosan body myopathy.
J Neuropathol Exp Neurol. 1992 Jan;51(1):24-35. Review.
PMID: 1311021 [PubMed - indexed for MEDLINE]

710: Litchy WJ, Engel AG.
Inclusion body myositis with cricopharyngeus muscle involvement and severe
dysphagia.
Muscle Nerve. 1992 Jan;15(1):115. No abstract available.
PMID: 1310156 [PubMed - indexed for MEDLINE]

711: Danon MJ, Friedman M.
Inclusion body myositis with cricopharyngeus muscle involvement and severe
dysphagia.
Muscle Nerve. 1992 Jan;15(1):115. No abstract available.
PMID: 1310155 [PubMed - indexed for MEDLINE]

712: Mendell JR, Sahenk Z, Gales T, Paul L.
Amyloid filaments in inclusion body myositis. Novel findings provide insight
into nature of filaments.
Arch Neurol. 1991 Dec;48(12):1229-34.
PMID: 1668977 [PubMed - indexed for MEDLINE]

713: Dalakas MC.
Polymyositis, dermatomyositis and inclusion-body myositis.
N Engl J Med. 1991 Nov 21;325(21):1487-98. Review. No abstract available.
PMID: 1658649 [PubMed - indexed for MEDLINE]

714: Higuchi I, Nerenberg M, Ijichi T, Fukunaga H, Arimura K, Usuki F, Kuriyama
M, Osame M.
Vacuolar myositis with expression of both MHC class I and class II antigens on
skeletal muscle fibers.
J Neurol Sci. 1991 Nov;106(1):60-6.
PMID: 1779240 [PubMed - indexed for MEDLINE]

715: Love LA, Leff RL, Fraser DD, Targoff IN, Dalakas M, Plotz PH, Miller FW.
A new approach to the classification of idiopathic inflammatory myopathy:
myositis-specific autoantibodies define useful homogeneous patient groups.
Medicine (Baltimore). 1991 Nov;70(6):360-74.
PMID: 1659647 [PubMed - indexed for MEDLINE]

716: [No authors listed]
Case records of the Massachusetts General Hospital. Weekly clinicopathological
exercises. Case 40-1991. A 48-year-old woman with progressive asymmetric
weakness of the extremities and neck flexor muscles.
N Engl J Med. 1991 Oct 3;325(14):1026-35. No abstract available.
PMID: 1653405 [PubMed - indexed for MEDLINE]

717: Askanas V, Serdaroglu P, Engel WK, Alvarez RB.
Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion
body myositis and oculopharyngeal muscular dystrophy.
Neurosci Lett. 1991 Sep 2;130(1):73-6.
PMID: 1660975 [PubMed - indexed for MEDLINE]

718: Iannaccone S, Zucconi M, Quattrini A, Nemni R, Comola M, Taccagni L,
Smirne S.
Early detection of skin and muscular involvement in Lafora disease.
J Neurol. 1991 Jul;238(4):217-20.
PMID: 1654400 [PubMed - indexed for MEDLINE]

719: Antoniades K, Taskos N, Mavromatis J, Sakkas L, Karakasis D.
Familial nemaline myopathy: case reports.
Oral Surg Oral Med Oral Pathol. 1991 Jul;72(1):51-4.
PMID: 1653926 [PubMed - indexed for MEDLINE]

720: Massa R, Weller B, Karpati G, Shoubridge E, Carpenter S.
Familial inclusion body myositis among Kurdish-Iranian Jews.
Arch Neurol. 1991 May;48(5):519-22.
PMID: 1850594 [PubMed - indexed for MEDLINE]

721: Hohlfeld R, Engel AG.
Coculture with autologous myotubes of cytotoxic T cells isolated from muscle in
inflammatory myopathies.
Ann Neurol. 1991 May;29(5):498-507.
PMID: 1830466 [PubMed - indexed for MEDLINE]

722: Verma A, Bradley WG, Adesina AM, Sofferman R, Pendlebury WW.
Inclusion body myositis with cricopharyngeus muscle involvement and severe
dysphagia.
Muscle Nerve. 1991 May;14(5):470-3.
PMID: 1651449 [PubMed - indexed for MEDLINE]

723: Lindberg C, Borg K, Edstrom L, Hedstrom A, Oldfors A.
Inclusion body myositis and Welander distal myopathy: a clinical,
neurophysiological and morphological comparison.
J Neurol Sci. 1991 May;103(1):76-81.
PMID: 1650819 [PubMed - indexed for MEDLINE]

724: Hohlfeld R, Engel AG, Ii K, Harper MC.
Polymyositis mediated by T lymphocytes that express the gamma/delta receptor.
N Engl J Med. 1991 Mar 28;324(13):877-81.
PMID: 1705662 [PubMed - indexed for MEDLINE]

725: Telerman-Toppet N, Bauherz G, Noel S.
Auriculo-ventricular block and distal myopathy with rimmed vacuoles and desmin
storage.
Clin Neuropathol. 1991 Mar-Apr;10(2):61-4.
PMID: 1647283 [PubMed - indexed for MEDLINE]

726: Purvis J, Fam AG, Lewis A.
Clinically unsuspected inclusion body myositis.
J Rheumatol. 1991 Feb;18(2):289-92.
PMID: 1850803 [PubMed - indexed for MEDLINE]

727: Kallajoki M, Hyypia T, Halonen P, Orvell C, Rima BK, Kalimo H.
Inclusion body myositis and paramyxoviruses.
Hum Pathol. 1991 Jan;22(1):29-32.
PMID: 1845865 [PubMed - indexed for MEDLINE]

728: Borg K, Tome FM, Edstrom L.
Intranuclear and cytoplasmic filamentous inclusions in distal myopathy
(Welander).
Acta Neuropathol (Berl). 1991;82(2):102-6.
PMID: 1656692 [PubMed - indexed for MEDLINE]

729: Halbig L, Goebel HH, Hopf HC, Moll R.
Spheroid-cytoplasmic complexes in a congenital myopathy.
Rev Neurol (Paris). 1991;147(4):300-7.
PMID: 1648255 [PubMed - indexed for MEDLINE]

730: Shousha S, Bull TB.
Intracellular inclusions in visceral myopathy.
J Pathol. 1990 Dec;162(4):355. No abstract available.
PMID: 1963194 [PubMed - indexed for MEDLINE]

731: Lindberg C, Oldfors A, Hedstrom A.
Inclusion body myositis: peripheral nerve involvement. Combined morphological
and electrophysiological studies on peripheral nerves.
J Neurol Sci. 1990 Nov;99(2-3):327-38.
PMID: 1964960 [PubMed - indexed for MEDLINE]

732: Sasaki M, Yoneyama H, Nonaka I.
Respiratory muscle involvement in nemaline myopathy.
Pediatr Neurol. 1990 Nov-Dec;6(6):425-7.
PMID: 1963532 [PubMed - indexed for MEDLINE]

733: Coquet M, Vital C, Julien J.
Presence of inclusion body myositis-like filaments in oculopharyngeal muscular
dystrophy. Ultrastructural study of 10 cases.
Neuropathol Appl Neurobiol. 1990 Oct;16(5):393-400.
PMID: 2175847 [PubMed - indexed for MEDLINE]

734: Joy JL, Oh SJ, Baysal AI.
Electrophysiological spectrum of inclusion body myositis.
Muscle Nerve. 1990 Oct;13(10):949-51.
PMID: 2172812 [PubMed - indexed for MEDLINE]

735: Helm TN, Valenzuela R, Bergfeld WF, Guitart J, Poolos CJ.
In vivo complement C3 binding to the intercellular substance and cytoplasm of
epidermal basal cells in a patient with scleroderma and inclusion body myositis.
J Am Acad Dermatol. 1990 Oct;23(4 Pt 1):753-4. No abstract available.
PMID: 2172335 [PubMed - indexed for MEDLINE]

736: Miller FW, Love LA, Barbieri SA, Balow JE, Plotz PH.
Lymphocyte activation markers in idiopathic myositis: changes with disease
activity and differences among clinical and autoantibody subgroups.
Clin Exp Immunol. 1990 Sep;81(3):373-9.
PMID: 2168821 [PubMed - indexed for MEDLINE]

737: Mhiri C, Gherardi R.
Inclusion body myositis in French patients. A clinicopathological evaluation.
Neuropathol Appl Neurobiol. 1990 Aug;16(4):333-44.
PMID: 2172855 [PubMed - indexed for MEDLINE]

738: Panegyres PK, Papadimitriou JM, Hollingsworth PN, Armstrong JA, Kakulas
BA.
Vesicular changes in the myopathies of AIDS. Ultrastructural observations and
their relationship to zidovudine treatment.
J Neurol Neurosurg Psychiatry. 1990 Aug;53(8):649-55.
PMID: 2170584 [PubMed - indexed for MEDLINE]

739: Martin JE, Swash M, Kamm MA, Mather K, Cox EL, Gray A.
Myopathy of internal anal sphincter with polyglucosan inclusions.
J Pathol. 1990 Jul;161(3):221-6.
PMID: 2167961 [PubMed - indexed for MEDLINE]

740: Dieler R, Schroder JM.
Lacunar dilatations of intrafusal and extrafusal terminal cisternae, annulate
lamellae, confronting cisternae and tubulofilamentous inclusions within the
spectrum of muscle and nerve fiber changes in myotonic dystrophy.
Pathol Res Pract. 1990 Jun;186(3):371-82.
PMID: 2143018 [PubMed - indexed for MEDLINE]

741: Emslie-Smith AM, Engel AG.
Microvascular changes in early and advanced dermatomyositis: a quantitative
study.
Ann Neurol. 1990 Apr;27(4):343-56.
PMID: 2353792 [PubMed - indexed for MEDLINE]

742: Fidzianska A, Goebel HH, Kleine M.
Neonatal form of nemaline myopathy, muscle immaturity, and a microvascular
injury.
J Child Neurol. 1990 Apr;5(2):122-6.
PMID: 2161030 [PubMed - indexed for MEDLINE]

743: Dumitru D, Newell-Eggert M.
Inclusion body myositis. An electrophysiologic study.
Am J Phys Med Rehabil. 1990 Feb;69(1):2-5.
PMID: 2154241 [PubMed - indexed for MEDLINE]

744: Schroder JM, Sommer C, Schmidt B.
Desmin and actin associated with cytoplasmic bodies in skeletal muscle fibers:
immunocytochemical and fine structural studies, with a note on unusual 18- to
20-nm filaments.
Acta Neuropathol (Berl). 1990;80(4):406-14.
PMID: 2173329 [PubMed - indexed for MEDLINE]

745: Figarella-Branger D, Pellissier JF, Bianco N, Devictor B, Toga M.
Inflammatory and non-inflammatory inclusion body myositis. Characterization of
the mononuclear cells and expression of the immunoreactive class I major
histocompatibility complex product.
Acta Neuropathol (Berl). 1990;79(5):528-36.
PMID: 2158202 [PubMed - indexed for MEDLINE]

746: Engel AG, Arahata K, Emslie-Smith A.
Immune effector mechanisms in inflammatory myopathies.
Res Publ Assoc Res Nerv Ment Dis. 1990;68:141-57. Review.
PMID: 2158132 [PubMed - indexed for MEDLINE]

747: Aasly J, Lindal S, Torbergsen T, Borud O, Mellgren SI.
Early mitochondrial changes in chronic progressive ocular myopathy.
Eur Neurol. 1990;30(6):314-8.
PMID: 1963142 [PubMed - indexed for MEDLINE]

748: Howl JD, Publicover SJ.
Lipidic mitochondrial inclusions in experimentally-induced in vitro myopathy of
mouse diaphragm.
Comp Biochem Physiol B. 1990;95(4):833-7.
PMID: 1693109 [PubMed - indexed for MEDLINE]

749: Kula RW, Sawchak JA, Sher JH.
Inclusion body myositis.
Curr Opin Rheumatol. 1989 Dec;1(4):460-7. Review. No abstract available.
PMID: 2562009 [PubMed - indexed for MEDLINE]

750: Targoff IN.
Immunologic aspects of myositis.
Curr Opin Rheumatol. 1989 Dec;1(4):432-42. Review. No abstract available.
PMID: 2562008 [PubMed - indexed for MEDLINE]

751: Bouchard JP, Gagne F, Tome FM, Brunet D.
Nuclear inclusions in oculopharyngeal muscular dystrophy in Quebec.
Can J Neurol Sci. 1989 Nov;16(4):446-50.
PMID: 2553230 [PubMed - indexed for MEDLINE]

752: Danon MJ, Friedman M.
Inclusion body myositis associated with progressive dysphagia: treatment with
cricopharyngeal myotomy.
Can J Neurol Sci. 1989 Nov;16(4):436-8.
PMID: 2553229 [PubMed - indexed for MEDLINE]

753: Riggs JE, Schochet SS Jr, Gutmann L, Lerfald SC.
Childhood onset inclusion body myositis mimicking limb-girdle muscular
dystrophy.
J Child Neurol. 1989 Oct;4(4):283-5.
PMID: 2551952 [PubMed - indexed for MEDLINE]

754: Kawabuchi M, Osame M, Aika Y, Kanaseki T.
Annulate lamellae-soleplate nuclei associations in skeletal muscle fibers of
rats during chronic high-dose exposure to neostigmine.
Anat Rec. 1989 Sep;225(1):1-10.
PMID: 2549812 [PubMed - indexed for MEDLINE]

755: Plotz PH, Dalakas M, Leff RL, Love LA, Miller FW, Cronin ME.
Current concepts in the idiopathic inflammatory myopathies: polymyositis,
dermatomyositis, and related disorders.
Ann Intern Med. 1989 Jul 15;111(2):143-57. Review.
PMID: 2662848 [PubMed - indexed for MEDLINE]

756: Tome FM, Askanas V, Engel WK, Alvarez RB, Lee CS.
Nuclear inclusions in innervated cultured muscle fibers from patients with
oculopharyngeal muscular dystrophy.
Neurology. 1989 Jul;39(7):926-32.
PMID: 2544827 [PubMed - indexed for MEDLINE]

757: Cohen MR, Sulaiman AR, Garancis JC, Wortmann RL.
Clinical heterogeneity and treatment response in inclusion body myositis.
Arthritis Rheum. 1989 Jun;32(6):734-40.
PMID: 2544185 [PubMed - indexed for MEDLINE]

758: Lotz BP, Engel AG, Nishino H, Stevens JC, Litchy WJ.
Inclusion body myositis. Observations in 40 patients.
Brain. 1989 Jun;112 ( Pt 3):727-47.
PMID: 2543478 [PubMed - indexed for MEDLINE]

759: Nishino H, Engel AG, Rima BK.
Inclusion body myositis: the mumps virus hypothesis.
Ann Neurol. 1989 Mar;25(3):260-4.
PMID: 2729916 [PubMed - indexed for MEDLINE]

760: Joy JL, Oh SJ.
Asymptomatic hyper-CK-emia: an electrophysiologic and histopathologic study.
Muscle Nerve. 1989 Mar;12(3):206-9.
PMID: 2725551 [PubMed - indexed for MEDLINE]

761: Emslie-Smith AM, Arahata K, Engel AG.
Major histocompatibility complex class I antigen expression, immunolocalization
of interferon subtypes, and T cell-mediated cytotoxicity in myopathies.
Hum Pathol. 1989 Mar;20(3):224-31.
PMID: 2470663 [PubMed - indexed for MEDLINE]

762: Sunohara N, Nonaka I, Kamei N, Satoyoshi E.
Distal myopathy with rimmed vacuole formation. A follow-up study.
Brain. 1989 Feb;112 ( Pt 1):65-83. Review.
PMID: 2645018 [PubMed - indexed for MEDLINE]

763: Mayer RJ, Lowe J, Lennox G, Landon M, MacLennan K, Doherty FJ.
Intermediate filament-ubiquitin diseases: implications for cell sanitization.
Biochem Soc Symp. 1989;55:193-201.
PMID: 2559734 [PubMed - indexed for MEDLINE]

764: Ono S, Inoue K, Mannen T, Mitake S, Shirai T, Kanda F, Jinnai K, Takahashi
K.
Intracytoplasmic inclusion bodies of the thalamus and the substantia nigra, and
Marinesco bodies in myotonic dystrophy: a quantitative morphological study.
Acta Neuropathol (Berl). 1989;77(4):350-6.
PMID: 2540609 [PubMed - indexed for MEDLINE]

765: Mizuno Y, Nakamura Y, Komiya K.
The spectrum of cytoplasmic body myopathy: report of a congenital severe case.
Brain Dev. 1989;11(1):20-5.
PMID: 2538089 [PubMed - indexed for MEDLINE]

766: Wintzen AR, Bots GT, de Bakker HM, Hulshof JH, Padberg GW.
Dysphagia in inclusion body myositis.
J Neurol Neurosurg Psychiatry. 1988 Dec;51(12):1542-5.
PMID: 2851642 [PubMed - indexed for MEDLINE]

767: Weis J, Schroder JM.
Adult polyglucosan body myopathy with subclinical peripheral neuropathy: case
report and review of diseases associated with polyglucosan body accumulation.
Clin Neuropathol. 1988 Nov-Dec;7(6):271-9. Review.
PMID: 2852083 [PubMed - indexed for MEDLINE]

768: Cole AJ, Kuzniecky R, Karpati G, Carpenter S, Andermann E, Andermann F.
Familial myopathy with changes resembling inclusion body myositis and
periventricular leucoencephalopathy. A new syndrome.
Brain. 1988 Oct;111 ( Pt 5):1025-37.
PMID: 2846114 [PubMed - indexed for MEDLINE]

769: Kingston WJ, Moxley RT 3rd.
Inflammatory myopathies.
Neurol Clin. 1988 Aug;6(3):545-61. Review.
PMID: 3065600 [PubMed - indexed for MEDLINE]

770: Abarbanel JM, Lichtenfeld Y, Zirkin H, Louzon Z, Osimani A, Farkash P,
Herishanu Y.
Inclusion body myositis in post-poliomyelitis muscular atrophy.
Acta Neurol Scand. 1988 Aug;78(2):81-4.
PMID: 2845701 [PubMed - indexed for MEDLINE]

771: Paulus W, Peiffer J, Becker I, Roggendorf W, Schumm F.
Adult-onset rod disease with abundant intranuclear rods.
J Neurol. 1988 Jul;235(6):343-7.
PMID: 2845006 [PubMed - indexed for MEDLINE]

772: Krendel DA, Gilchrist JM, Bossen EH.
Distal vacuolar myopathy with complete heart block.
Arch Neurol. 1988 Jun;45(6):698-9.
PMID: 3369979 [PubMed - indexed for MEDLINE]

773: Kawabuchi M, Kanaseki T.
Origin of true intranuclear inclusions in the soleplate region of rat skeletal
muscle fibers following chronic daily administration of neostigmine.
Fukuoka Igaku Zasshi. 1988 Jun;79(6):440-3. No abstract available.
PMID: 2852631 [PubMed - indexed for MEDLINE]

774: Arahata K, Engel AG.
Monoclonal antibody analysis of mononuclear cells in myopathies. V:
Identification and quantitation of T8+ cytotoxic and T8+ suppressor cells.
Ann Neurol. 1988 May;23(5):493-9.
PMID: 2968776 [PubMed - indexed for MEDLINE]

775: Lowe J, Blanchard A, Morrell K, Lennox G, Reynolds L, Billett M, Landon M,
Mayer RJ.
Ubiquitin is a common factor in intermediate filament inclusion bodies of
diverse type in man, including those of Parkinson's disease, Pick's disease, and
Alzheimer's disease, as well as Rosenthal fibres in cerebellar astrocytomas,
cytoplasmic bodies in muscle, and mallory bodies in alcoholic liver disease.
J Pathol. 1988 May;155(1):9-15.
PMID: 2837558 [PubMed - indexed for MEDLINE]

776: Arahata K, Engel AG.
Monoclonal antibody analysis of mononuclear cells in myopathies. IV:
Cell-mediated cytotoxicity and muscle fiber necrosis.
Ann Neurol. 1988 Feb;23(2):168-73.
PMID: 3288082 [PubMed - indexed for MEDLINE]

777: Comola M, Johnson MA, Howel D, Brunsdon C.
Spatial distribution of muscle necrosis in biopsies from patients with
inflammatory muscle disorders.
J Neurol Sci. 1987 Dec;82(1-3):229-44.
PMID: 2831309 [PubMed - indexed for MEDLINE]

778: Martinez BA, Lake BD.
Childhood nemaline myopathy: a review of clinical presentation in relation to
prognosis.
Dev Med Child Neurol. 1987 Dec;29(6):815-20. Review. No abstract available.
PMID: 2826280 [PubMed - indexed for MEDLINE]

779: Schmalbruch H, Kamieniecka Z, Arroe M.
Early fatal nemaline myopathy: case report and review.
Dev Med Child Neurol. 1987 Dec;29(6):800-4. Review.
PMID: 2826279 [PubMed - indexed for MEDLINE]

780: Ono S, Inoue K, Mannen T, Kanda F, Jinnai K, Takahashi K.
Neuropathological changes of the brain in myotonic dystrophy--some new
observations.
J Neurol Sci. 1987 Nov;81(2-3):301-20.
PMID: 3694233 [PubMed - indexed for MEDLINE]

781: Ringel SP, Kenny CE, Neville HE, Giorno R, Carry MR.
Spectrum of inclusion body myositis.
Arch Neurol. 1987 Nov;44(11):1154-7.
PMID: 2823752 [PubMed - indexed for MEDLINE]

782: Reyes MG, Goldbarg H, Fresco K, Bouffard A.
Zebra body myopathy: a second case of ultrastructurally distinct congenital
myopathy.
J Child Neurol. 1987 Oct;2(4):307-10.
PMID: 2821096 [PubMed - indexed for MEDLINE]

783: Calabrese LH, Mitsumoto H, Chou SM.
Inclusion body myositis presenting as treatment-resistant polymyositis.
Arthritis Rheum. 1987 Apr;30(4):397-403.
PMID: 3034295 [PubMed - indexed for MEDLINE]

784: Dau PC.
Leukocytapheresis in inclusion body myositis.
J Clin Apher. 1987;3(3):167-70.
PMID: 3558342 [PubMed - indexed for MEDLINE]

785: Bardosi A, Dickmann U.
Necrotizing myopathy with paracrystalline inclusion bodies in hypervitaminosis
E.
Acta Neuropathol (Berl). 1987;75(2):166-72.
PMID: 2829497 [PubMed - indexed for MEDLINE]

786: Fardeau M.
Some orthodox or non-orthodox considerations on congenital myopathies.
Electroencephalogr Clin Neurophysiol Suppl. 1987;39:85-90. No abstract
available.
PMID: 2820694 [PubMed - indexed for MEDLINE]

787: Ho KL.
Crystalloid bodies in skeletal muscle of hypothyroid myopathy. Ultrastructural
and histochemical studies.
Acta Neuropathol (Berl). 1987;74(1):22-32.
PMID: 2444062 [PubMed - indexed for MEDLINE]

788: Danon MJ, Perurena OH, Ronan S, Manaligod JR.
Inclusion body myositis associated with systemic sarcoidosis.
Can J Neurol Sci. 1986 Nov;13(4):334-6.
PMID: 3779534 [PubMed - indexed for MEDLINE]

789: van Munster ET, Joosten EM, van Munster-Uijtdehaage MA, Kruls HJ, ter Laak
HJ.
The rigid spine syndrome.
J Neurol Neurosurg Psychiatry. 1986 Nov;49(11):1292-7.
PMID: 3025374 [PubMed - indexed for MEDLINE]

790: Kelly JJ Jr, Madoc-Jones H, Adelman LS, Andres PL, Munsat TL.
Total body irradiation not effective in inclusion body myositis.
Neurology. 1986 Sep;36(9):1264-6.
PMID: 3748397 [PubMed - indexed for MEDLINE]

791: Chou SM.
Inclusion body myositis: a chronic persistent mumps myositis?
Hum Pathol. 1986 Aug;17(8):765-77.
PMID: 3015764 [PubMed - indexed for MEDLINE]

792: Engel AG, Arahata K.
Mononuclear cells in myopathies: quantitation of functionally distinct subsets,
recognition of antigen-specific cell-mediated cytotoxicity in some diseases, and
implications for the pathogenesis of the different inflammatory myopathies.
Hum Pathol. 1986 Jul;17(7):704-21.
PMID: 3459704 [PubMed - indexed for MEDLINE]

793: Chou SM, Mizuno Y.
Induction of spheroid cytoplasmic bodies in a rat muscle by local tetanus.
Muscle Nerve. 1986 Jun;9(5):455-64.
PMID: 3014329 [PubMed - indexed for MEDLINE]

794: Pratt MF, Meyers PK.
Oculopharyngeal muscular dystrophy: recent ultrastructural evidence for
mitochondrial abnormalities.
Laryngoscope. 1986 Apr;96(4):368-73.
PMID: 3007900 [PubMed - indexed for MEDLINE]

795: Lazaro RP, Barron KD, Dentinger MP, Lava NS.
Inclusion body myositis: case reports and a reappraisal of an underrecognized
type of inflammatory myopathy.
Mt Sinai J Med. 1986 Feb;53(2):137-44. No abstract available.
PMID: 3010093 [PubMed - indexed for MEDLINE]

796: Arahata K, Engel AG.
Monoclonal antibody analysis of mononuclear cells in myopathies. III:
Immunoelectron microscopy aspects of cell-mediated muscle fiber injury.
Ann Neurol. 1986 Feb;19(2):112-25.
PMID: 3008636 [PubMed - indexed for MEDLINE]

797: Gutmann L, Govindan S, Riggs JE, Schochet SS Jr.
Inclusion body myositis and Sjogren's syndrome.
Arch Neurol. 1985 Oct;42(10):1021-2. No abstract available.
PMID: 2994608 [PubMed - indexed for MEDLINE]

798: Bucher HU, Boltshauser E, Briner J.
Neonatal nemaline myopathy presenting with multiple joint contractures.
Eur J Pediatr. 1985 Sep;144(3):288-90.
PMID: 2414108 [PubMed - indexed for MEDLINE]

799: Goebel HH, Trautmann F, Dippold W.
Recent advances in the morphology of myositis.
Pathol Res Pract. 1985 Jul;180(1):1-9. Review.
PMID: 2994026 [PubMed - indexed for MEDLINE]

800: Amir N, Chemke J, Shapira Y.
Familial dysautonomia manifesting as neonatal nemaline myopathy.
Pediatr Neurol. 1985 Jul-Aug;1(4):249-51.
PMID: 2854735 [PubMed - indexed for MEDLINE]

801: Yood RA, Smith TW.
Inclusion body myositis and systemic lupus erythematosus.
J Rheumatol. 1985 Jun;12(3):568-70.
PMID: 2995660 [PubMed - indexed for MEDLINE]

802: Mastaglia FL, Ojeda VJ.
Inflammatory myopathies: Part 1.
Ann Neurol. 1985 Mar;17(3):215-27.
PMID: 2986525 [PubMed - indexed for MEDLINE]

803: Lane RJ, Fulthorpe JJ, Hudgson P.
Inclusion body myositis: a case with associated collagen vascular disease
responding to treatment.
J Neurol Neurosurg Psychiatry. 1985 Mar;48(3):270-3.
PMID: 2984335 [PubMed - indexed for MEDLINE]

804: Chou SM.
Inclusion body myositis. A possible chronic persistent muscle infection by
mumps virus.
Cleve Clin Q. 1985 Winter;52(4):583-9. No abstract available.
PMID: 3830473 [PubMed - indexed for MEDLINE]

805: Jones JG, Factor SM.
Familial congestive cardiomyopathy with nemaline rods in heart and skeletal
muscle.
Virchows Arch A Pathol Anat Histopathol. 1985;408(2-3):307-12.
PMID: 3002014 [PubMed - indexed for MEDLINE]

806: Canal N, Comi GC, Comola M, Testa D, Mora M, Cornelio F.
Centronuclear myopathy with unusual mitochondrial abnormalities.
Clin Neuropathol. 1985 Jan-Feb;4(1):23-7.
PMID: 2983917 [PubMed - indexed for MEDLINE]

807: Arahata K, Engel AG.
Monoclonal antibody analysis of mononuclear cells in myopathies. I:
Quantitation of subsets according to diagnosis and sites of accumulation and
demonstration and counts of muscle fibers invaded by T cells.
Ann Neurol. 1984 Aug;16(2):193-208.
PMID: 6383191 [PubMed - indexed for MEDLINE]

808: Engel AG, Arahata K.
Monoclonal antibody analysis of mononuclear cells in myopathies. II: Phenotypes
of autoinvasive cells in polymyositis and inclusion body myositis.
Ann Neurol. 1984 Aug;16(2):209-15.
PMID: 6089646 [PubMed - indexed for MEDLINE]

809: Smith TW, Chad D.
Intranuclear inclusions in oculopharyngeal dystrophy.
Muscle Nerve. 1984 May;7(4):339-40. No abstract available.
PMID: 6328293 [PubMed - indexed for MEDLINE]

810: Kagen LJ.
Less common causes of myositis.
Clin Rheum Dis. 1984 Apr;10(1):175-87. No abstract available.
PMID: 6329593 [PubMed - indexed for MEDLINE]

811: Wakayama Y, Okayasu H, Kumagai T.
Quantitative freeze-fracture electron microscopic study of muscle plasma
membrane of experimental anoxic myopathy.
J Neurol Sci. 1984 Mar;63(3):411-21.
PMID: 6327922 [PubMed - indexed for MEDLINE]

812: Tateishi J, Nagara H, Ohta M, Matsumoto T, Fukunaga H, Shida K.
Intranuclear inclusions in muscle, nervous tissue, and adrenal gland.
Acta Neuropathol (Berl). 1984;63(1):24-32.
PMID: 6328832 [PubMed - indexed for MEDLINE]

813: Kuzuhara S, Nakanishi T.
Tubulomembranous and fingerprint-like inclusions in biopsied muscle of distal
myopathy with rimmed vacuoles.
Acta Neuropathol (Berl). 1984;62(3):194-200.
PMID: 6320578 [PubMed - indexed for MEDLINE]

814: Riggs JE, Schochet SS Jr, Gutmann L, McComas CF, Rogers JS 2nd.
Inclusion body myositis and chronic immune thrombocytopenia.
Arch Neurol. 1984 Jan;41(1):93-5.
PMID: 6316880 [PubMed - indexed for MEDLINE]

815: Gibbels E, Henke U, Schadlich HJ, Haupt WF, Fiehn W.
Cylindrical spirals in skeletal muscle: a further observation with clinical,
morphological, and biochemical analysis.
Muscle Nerve. 1983 Nov-Dec;6(9):646-55.
PMID: 6318106 [PubMed - indexed for MEDLINE]

816: Tsujihata M, Shimomura C, Yoshimura T, Sato A, Ogawa T, Tsuji Y, Nagataki
S, Matsuo T.
Fatal neonatal nemaline myopathy: a case report.
J Neurol Neurosurg Psychiatry. 1983 Sep;46(9):856-9.

PMID: 6311989 [PubMed - indexed for MEDLINE]

817: Eisen A, Berry K, Gibson G.
Inclusion body myositis (IBM): myopathy or neuropathy?
Neurology. 1983 Sep;33(9):1109-14.
PMID: 6310442 [PubMed - indexed for MEDLINE]

818: Coquet M, Vallat JM, Vital C, Fournier M, Barat M, Orgogozo JM, Julien J,
Loiseau P.
Nuclear inclusions in oculopharyngeal dystrophy. An ultrastructural study of
six cases.
J Neurol Sci. 1983 Jul;60(1):151-6.
PMID: 6308176 [PubMed - indexed for MEDLINE]

819: Yarom R, Meyer S, More R, Liebergall M, Eldor A.
Platelet abnormalities in muscular dystrophy.
Thromb Haemost. 1983 Jun 28;49(3):168-72.
PMID: 6308847 [PubMed - indexed for MEDLINE]

820: Oh SJ, Meyers GJ, Wilson ER Jr, Alexander CB.
A benign form of reducing body myopathy.
Muscle Nerve. 1983 May;6(4):278-82. No abstract available.
PMID: 6306460 [PubMed - indexed for MEDLINE]

821: Smith R, Hughes RL, Borensztajn J, Segura RP, Sahgal V.
Focal muscle cramps in a young man. Possible myopathy with tubular aggregates.
Chest. 1983 May;83(5):795-800. No abstract available.
PMID: 6301765 [PubMed - indexed for MEDLINE]

822: Lullmann-Rauch R, Nassberger L.
Citalopram-induced generalized lipidosis in rats.
Acta Pharmacol Toxicol (Copenh). 1983 Mar;52(3):161-7.
PMID: 6303044 [PubMed - indexed for MEDLINE]

823: Jones GE, Severs NJ, Witkowski JA.
Freeze-fracture analysis of plasma membranes in Duchenne muscular dystrophy. A
study using cultured skin fibroblasts.
J Neurol Sci. 1983 Feb;58(2):185-93.
PMID: 6300339 [PubMed - indexed for MEDLINE]

824: Schmitt HP, Lenard HG.
Intrinsic laryngeal muscles in oculocraniosomatic syndrome (OCSS). An autopsy
study.
Arch Otorhinolaryngol. 1983;237(2):153-60.
PMID: 6847514 [PubMed - indexed for MEDLINE]

825: Osborn M, Goebel HH.
The cytoplasmic bodies in a congenital myopathy can be stained with antibodies
to desmin, the muscle-specific intermediate filament protein.
Acta Neuropathol (Berl). 1983;62(1-2):149-52.
PMID: 6318501 [PubMed - indexed for MEDLINE]

826: Goebel HH, Heckmann C, Schulz F, Schaake T.
Ultrastructural aspects of striated muscle fibers in health and disease.
Acta Histochem Suppl. 1983;28:85-99.
PMID: 6310687 [PubMed - indexed for MEDLINE]

827: Stuhlfauth I, Jennekens FG, Willemse J, Jockusch BM.
Congenital nemaline myopathy. II. Quantitative changes in alpha-actinin and
myosin in skeletal muscle.
Muscle Nerve. 1983 Jan;6(1):69-74.
PMID: 6302503 [PubMed - indexed for MEDLINE]

828: Jennekens FG, Roord JJ, Veldman H, Willemse J, Jockusch BM.
Congenital nemaline myopathy. I. Defective organization of alpha-actinin is
restricted to muscle.
Muscle Nerve. 1983 Jan;6(1):61-8. No abstract available.
PMID: 6302502 [PubMed - indexed for MEDLINE]

829: Danon MJ, Reyes MG, Perurena OH, Masdeu JC, Manaligod JR.
Inclusion body myositis. A corticosteroid-resistant idiopathic inflammatory
myopathy.
Arch Neurol. 1982 Dec;39(12):760-4.
PMID: 6291495 [PubMed - indexed for MEDLINE]

830: Scarlato G, Pellegrini G, Moggio M, Meola G, Cordone G, Minetti C, Lester
A.
Familial nemaline myopathy.
Neuropediatrics. 1982 Nov;13(4):211-5.
PMID: 6296713 [PubMed - indexed for MEDLINE]

831: Julien J, Vital C, Vallat JM, Lagueny A, Sapina D.
Inclusion body myositis. Clinical, biological and ultrastructural study.
J Neurol Sci. 1982 Jul;55(1):15-24.
PMID: 6286889 [PubMed - indexed for MEDLINE]

832: Mikol J, Felten-Papaiconomou A, Ferchal F, Perol Y, Gautier B, Haguenau M,
Pepin B.
Inclusion-body myositis: clinicopathological studies and isolation of an
adenovirus type 2 from muscle biopsy specimen.
Ann Neurol. 1982 Jun;11(6):576-81. No abstract available.
PMID: 6287912 [PubMed - indexed for MEDLINE]

833: Fukuhara N, Kumamoto T, Tsubaki T, Mayuzumi T, Nitta H.
Oculopharyngeal muscular dystrophy and distal myopathy. Intrafamilial
difference in the onset and distribution of muscular involvement.
Acta Neurol Scand. 1982 May;65(5):458-67.
PMID: 7113658 [PubMed - indexed for MEDLINE]

834: Chad D, Good P, Adelman L, Bradley WG, Mills J.
Inclusion body myositis associated with Sjogren's syndrome.
Arch Neurol. 1982 Mar;39(3):186-8. No abstract available.
PMID: 6978124 [PubMed - indexed for MEDLINE]

835: Hiraoka A, Kitani T, Takahashi M, Tarui S.
Lymphocyte abnormality in human myotonic dystrophy and experimental
drug-induced myotonia.
Neurology. 1982 Feb;32(2):138-42.
PMID: 6275309 [PubMed - indexed for MEDLINE]

836: Wolburg H, Schlote W, Langohr HD, Peiffer J, Reiher KH, Heckl RW.
Slowly progressive congenital myopathy with cytoplasmic bodies--report of two
cases and a review of the literature.
Clin Neuropathol. 1982;1(2):55-66.
PMID: 6301720 [PubMed - indexed for MEDLINE]

837: Goebel HH, Schloon H, Lenard HG.
Congenital myopathy with cytoplasmic bodies.
Neuropediatrics. 1981 May;12(2):166-80.
PMID: 6267501 [PubMed - indexed for MEDLINE]

838: Shapira YA, Yarom R, Blank A.
Nemaline myopathy and a mitochondrial neuromuscular disorder in one family.
Neuropediatrics. 1981 May;12(2):152-65.
PMID: 6267500 [PubMed - indexed for MEDLINE]

839: Porter CB, Hinthorn DR, Couchonnal G, Watanabe I, Caveny EA, Goldman B,
Lash R, Holmes F, Liu C.
Simultaneous Streptococcus and picornavirus infection. Muscle involvement in
acute rhabdomyolysis.
JAMA. 1981 Apr 17;245(15):1545-7.
PMID: 6259382 [PubMed - indexed for MEDLINE]

840: Fukuhara N, Kumamoto T, Hirahara H, Tsubaki T.
A new myopathy with tubulomembranous inclusions.
J Neurol Sci. 1981 Apr;50(1):95-107.
PMID: 6262462 [PubMed - indexed for MEDLINE]

841: Edstrom L, Wroblewski R.
Sarcoplasmic bodies in distal myopathy compared with nemaline rods.
J Neurol Sci. 1981 Mar;49(3):341-52.
PMID: 6260902 [PubMed - indexed for MEDLINE]

842: Herzberg L, Harnett GB, Papadimitriou J, Tan N.
Muscle disease and viruses.
Clin Exp Neurol. 1981;17:135-8. No abstract available.
PMID: 7346194 [PubMed - indexed for MEDLINE]

843: Coquet M, Vallat JM, Latapie JL.
Basophilic inclusions in skeletal muscle from two cases of hypothyroid
myopathy.
Acta Neuropathol Suppl (Berl). 1981;7:320-2.
PMID: 6261518 [PubMed - indexed for MEDLINE]

844: Tome FM, Fardeau M, Lebon P, Chevallay M.
Inclusion body myositis.
Acta Neuropathol Suppl (Berl). 1981;7:287-91.
PMID: 6261517 [PubMed - indexed for MEDLINE]

845: Vaccario ML, Scoppetta C, Bracaglia R, Uncini A.
Sporadic distal myopathy.
J Neurol. 1981;224(4):291-5.
PMID: 6162931 [PubMed - indexed for MEDLINE]

846: Edstrom L, Thornell LE, Eriksson A.
A new type of hereditary distal myopathy with characteristic sarcoplasmic
bodies and intermediate (skeletin) filaments.
J Neurol Sci. 1980 Aug;47(2):171-90.
PMID: 6251174 [PubMed - indexed for MEDLINE]

847: Fukunaga H, Osame M, Igata A.
A case of nemaline myopathy with ophthalmoplegia and mitochondrial
abnormalities.
J Neurol Sci. 1980 May;46(2):169-77.
PMID: 6247453 [PubMed - indexed for MEDLINE]

848: Peyronnard JM, Charron L, Bellavance A, Marchand L.
Neuropathy and mitochondrial myopathy.
Ann Neurol. 1980 Mar;7(3):262-8.
PMID: 6252825 [PubMed - indexed for MEDLINE]

849: Jadro-Santel D, Grcevic N, Dogan S, Franjic J, Benc H.
Centronuclear myopathy with type I fibre hypotrophy and "fingerprint"
inclusions associated with Marfan's syndrome.
J Neurol Sci. 1980 Feb;45(1):43-56.
PMID: 6244371 [PubMed - indexed for MEDLINE]

850: Kornfeld M.
Mixed nemaline-mitochondrial "myopathy".
Acta Neuropathol (Berl). 1980;51(3):185-9.
PMID: 6255722 [PubMed - indexed for MEDLINE]

851: Pena CE.
Intracytoplasmic neuronal inclusions in the human thalamus. Light-microscopic,
histochemical, and ultrastructural observations.
Acta Neuropathol (Berl). 1980;52(2):157-9.
PMID: 6254321 [PubMed - indexed for MEDLINE]

852: Bonilla E, Schotland DL, Di Mauro S.
Ultrastructural study of globular inclusions in human skeletal muscle
mitochondria.
Acta Neuropathol (Berl). 1980;52(1):35-40.
PMID: 6254319 [PubMed - indexed for MEDLINE]

853: Matsubara S.
Ultrastructural changes in granulomatous myopathy.
Acta Neuropathol (Berl). 1980;50(2):91-6.
PMID: 6249063 [PubMed - indexed for MEDLINE]

854: Tome FM, Fardeau M.
Nuclear inclusions in oculopharyngeal dystrophy.
Acta Neuropathol (Berl). 1980;49(1):85-7.
PMID: 6243839 [PubMed - indexed for MEDLINE]

855: Matsubara S, Mair WG.
Ultrastructural changes in polymyositis.
Brain. 1979 Dec;102(4):701-25.
PMID: 228791 [PubMed - indexed for MEDLINE]

856: Green RJ, Webb JN, Maxwell MH.
The nature of virus-like particles in the paraxial muscles of idiopathic
scoliosis.
J Pathol. 1979 Sep;129(1):9-12.
PMID: 230331 [PubMed - indexed for MEDLINE]

857: Oshima Y, Becker LE, Armstrong DL.
An electron microscopic study of childhood dermatomyositis.
Acta Neuropathol (Berl). 1979 Aug;47(3):189-96.
PMID: 225919 [PubMed - indexed for MEDLINE]

858: Matsubara S, Mair WG.
Fingerprint inclusions and circular structures in the muscle. Report of a case.
Acta Neuropathol (Berl). 1979 Jul 13;47(2):161-2.
PMID: 224637 [PubMed - indexed for MEDLINE]

859: Bradley R.
A primary bovine skeletal myopathy with absence of Z discs, sarcoplasmic
inclusions, myofibrillar hypoplasia and nuclear abnormality.
J Comp Pathol. 1979 Jul;89(3):381-8. No abstract available.
PMID: 231056 [PubMed - indexed for MEDLINE]

860: Kosaka K, Mehraein P.
Dementia-Parkinsonism syndrome with numerous Lewy bodies and senile plaques in
cerebral cortex.
Arch Psychiatr Nervenkr. 1979 Apr 12;226(4):241-50.
PMID: 222231 [PubMed - indexed for MEDLINE]

861: Bonsett CA, Rudman A, Elliott AY.
Intracellular lipid in pseudohypertrophic muscular dystrophy tissue culture.
J Indiana State Med Assoc. 1979 Mar;72(3):184-7. No abstract available.
PMID: 217934 [PubMed - indexed for MEDLINE]

862: Olmos L, Hunziker N, Laugier P.
Microcylinders of endoplasmic reticulum in histiocytes in patients suffering
from Degos' syndrome and dermatomyositis.
Br J Dermatol. 1979 Feb;100(2):137-45.
PMID: 218603 [PubMed - indexed for MEDLINE]

863: de Coster W, de Reuck J, vander Eecken H.
Nemaline bodies in a progressive infantile neuromuscular disorder.
J Neurol. 1978 Sep 12;219(1):37-45.
PMID: 81283 [PubMed - indexed for MEDLINE]

864: Scelsi R, Poggi P, Nappi G, Sandrini G.
Peripheral microcirculatory lesions in myotonic dystrophy. A light and an
electron microscopic study on digital biopsies.
Acta Neurol (Napoli). 1978 Mar-Apr;33(2):137-48. No abstract available.
PMID: 207159 [PubMed - indexed for MEDLINE]

865: Brownell AK, Engel AG.
Experimental lipid storage myopathy. A quantitative ultrastructural and
biochemical study.
J Neurol Sci. 1978 Jan;35(1):31-41.
PMID: 203664 [PubMed - indexed for MEDLINE]

866: Johnson MA.
Nuclear abnormalities in muscle regenerating after Echo 9 virus infection in
mice.
J Neurol Sci. 1978 Jan;35(1):117-33. No abstract available.
PMID: 203663 [PubMed - indexed for MEDLINE]

867: Carpenter S, Karpati G, Heller I, Eisen A.
Inclusion body myositis: a distinct variety of idiopathic inflammatory
myopathy.
Neurology. 1978 Jan;28(1):8-17.
PMID: 201886 [PubMed - indexed for MEDLINE]

868: Schaumburg HH, Powers JM, Raine CS, Spencer PS, Griffin JW, Prineas JW,
Boehme DM.
Adrenomyeloneuropathy: a probable variant of adrenoleukodystrophy. II. General
pathologic, neuropathologic, and biochemical aspects.
Neurology. 1977 Dec;27(12):1114-9.
PMID: 200862 [PubMed - indexed for MEDLINE]

869: Ketelsen UP, Beckmann R, Zimmermann H, Sauer M.
Inclusion body myositis. A "slow-virus" infection of skeletal musculature?
Klin Wochenschr. 1977 Nov 1;55(21):1063-6.
PMID: 926717 [PubMed - indexed for MEDLINE]

870: Cullen MJ, Parsons R.
Inclusion bodies in muscular dystrophy.
Lancet. 1977 Oct 29;2(8044):929. No abstract available.
PMID: 72267 [PubMed - indexed for MEDLINE]

871: Markesbery WR, Griggs RC, Herr B.
Distal myopathy: electron microscopic and histochemical studies.
Neurology. 1977 Aug;27(8):727-35.
PMID: 196233 [PubMed - indexed for MEDLINE]

872: Payne CM, Curless RG.
Fingerprint inclusions. Ultrastructural demonstration of muscle fiber type
specificity.
J Neurol Sci. 1977 Apr;31(3):379-86.
PMID: 191570 [PubMed - indexed for MEDLINE]

873: Sahgal V, Sahgal S.
Department of Neurology, Northwestern University Medical School, Chicago,
Illinois.
Acta Neuropathol (Berl). 1977 Mar 31;37(3):225-30.
PMID: 193343 [PubMed - indexed for MEDLINE]

874: Cornelio F, Di Donato S, Peluchetti D, Bizze A, Bertagnolio B, D'Angelo A,
Wiesmann U.
Fatal cases of lipid storage myopathy with carnitine deficiency.
J Neurol Neurosurg Psychiatry. 1977 Feb;40(2):170-8.
PMID: 194020 [PubMed - indexed for MEDLINE]

875: Yarom R, Shapira Y.
Myosin degeneration in a congenital myopathy.
Arch Neurol. 1977 Feb;34(2):114-5.
PMID: 189737 [PubMed - indexed for MEDLINE]

876: Yagishita S, Itoh Y, Nakano T.
Corpora amylacea in the peripheral nerve axons.
Acta Neuropathol (Berl). 1977 Jan 31;37(1):73-6.
PMID: 190849 [PubMed - indexed for MEDLINE]

877: Wyatt PR, Cox DM.
Duchenne's muscular dystrophy: studies in cultured fibroblasts.
Lancet. 1977 Jan 22;1(8004):172-4.
PMID: 64702 [PubMed - indexed for MEDLINE]

878: Kamieniecka Z.
Myopathies with abnormal mitochondria. A clinical, histological, and
electrophysiological study.
Acta Neurol Scand. 1977 Jan;55(1):57-75.
PMID: 190845 [PubMed - indexed for MEDLINE]

879: Dyck PJ.
Investigative approaches: pathologic and morphometric three-dimensional studies
in peripheral neuropathy.
Adv Neurol. 1977;17:249-63. No abstract available.
PMID: 18910 [PubMed - indexed for MEDLINE]

880: Taylor JF, Fluck D, Fluck D.
Tropical myositis: ultrastructural studies.
J Clin Pathol. 1976 Dec;29(12):1081-4.
PMID: 188870 [PubMed - indexed for MEDLINE]

881: Boudin G, Mikol J, Guillard A, Engel AG.
Fatal systemic carnitine deficiency with lipid storage in skeletal muscle,
heart, liver and kidney.
J Neurol Sci. 1976 Dec;30(2-3):313-25.
PMID: 187738 [PubMed - indexed for MEDLINE]

882: Cumming WJ, Hardy M, Hudgson P, Walls J.
Carnitine-palmityl-transferase deficiency.
J Neurol Sci. 1976 Dec;30(2-3):247-58.
PMID: 187736 [PubMed - indexed for MEDLINE]

883: Payne CM, Curless RG.
Concentric laminated bodies. Ultrastructural demonstration of muscle fiber type
specificity.
J Neurol Sci. 1976 Oct;29(2-4):311-22.
PMID: 185337 [PubMed - indexed for MEDLINE]

884: Fardeau M, Tome FM, Derambure S.
Familial fingerprint body myopathy.
Arch Neurol. 1976 Oct;33(10):724-5.
PMID: 184767 [PubMed - indexed for MEDLINE]

885: Carpenter S, Karpati G, Rothman S, Watters G.
The childhood type of dermatomyositis.
Neurology. 1976 Oct;26(10):952-62.
PMID: 183170 [PubMed - indexed for MEDLINE]

886: Oteruelo FT.
Intranuclear inclusions in a myopathy of late onset.
Virchows Arch B Cell Pathol. 1976 May 26;20(4):319-24.
PMID: 180655 [PubMed - indexed for MEDLINE]

887: Benke B.
Mass occurrence of multilamellar bodies in myopathy.
Virchows Arch B Cell Pathol. 1976 Feb 11;20(1):77-84.
PMID: 176775 [PubMed - indexed for MEDLINE]

888: Stromer MH, Tabatabai LB, Robson RM, Goll DE, Zeece MG.
Nemaline myopathy, an integrated study: selective extraction.
Exp Neurol. 1976 Feb;50(2):402-21. No abstract available.
PMID: 174926 [PubMed - indexed for MEDLINE]

889: Schiffer D, Giordana MT, Monga G, Mollo F.
Histochemistry and electron microscopy of muscle fibres in a case of congenital
paramyotonia.
J Neurol. 1976 Jan 14;211(2):125-33.
PMID: 55468 [PubMed - indexed for MEDLINE]

890: Sreter FA, Astrom KE, Romanul FC, Young RR, Jones HR Jr.
Characteristics of myosin in nemaline myopathy.
J Neurol Sci. 1976 Jan;27(1):99-116.
PMID: 175135 [PubMed - indexed for MEDLINE]

891: Okamura K, Santa T, Nagae K, Omae T.
Congenital oculoskeletal myopathy with abnormal muscle and liver mitochondria.
J Neurol Sci. 1976 Jan;27(1):79-91.
PMID: 175134 [PubMed - indexed for MEDLINE]

892: Pachter BR, Davidowitz J, Breinin GM.
Structural alterations of the junctional region in extraocular muscle of
dystrophic mice. II. Hypertrophy of the neuromuscular junctional apparatus.
Am J Pathol. 1976 Jan;82(01):111-8.
PMID: 174437 [PubMed - indexed for MEDLINE]

893: Davidowitz J, Pachter BR, Philips G, Breinin GM.
Structural alterations of the junctional region in extraocular muscle of
dystrophic mice. I. Modifications of sole-plate nuclei.
Am J Pathol. 1976 Jan;82(01):101-10.
PMID: 174436 [PubMed - indexed for MEDLINE]

894: Bender AN, Engel WK.
Light-cored dense particles in mitochondria of a patient with skeletal muscle
and myocardial disease.
J Neuropathol Exp Neurol. 1976 Jan;35(1):46-52.
PMID: 173811 [PubMed - indexed for MEDLINE]

895: Korenyi-Both A, Lapis K, Gallai M, Szobor A.
Fine structural alterations of muscle fibers in diseases accompanied by
myotonia.
Beitr Pathol. 1975 Dec;156(3):241-56.
PMID: 1218025 [PubMed - indexed for MEDLINE]

896: Isaacs H, Muncke G.
Idiopathic cardiomyopathy and skeletal muscle abnormality.
Am Heart J. 1975 Dec;90(6):767-73.
PMID: 173170 [PubMed - indexed for MEDLINE]

897: Hudgson P, Fulthorpe JJ.
The pathology of type II skeletal muscle glycogenosis. A light and
electron-microscopic study.
J Pathol. 1975 Jul;116(3):139-47.
PMID: 172619 [PubMed - indexed for MEDLINE]

898: Hughes JT, Esiri MM.
Ultrastructural studies in human polymyositis.
J Neurol Sci. 1975 Jul;25(3):347-60.
PMID: 169326 [PubMed - indexed for MEDLINE]

899: Shaw C, Sumi SM.
Nonviral intranuclear filamentous inclusions.
Arch Neurol. 1975 Jul;32(7):428-32.
PMID: 166631 [PubMed - indexed for MEDLINE]

900: Yarrington JT, Whiehair CK.
Ultrastructure of gastointestinal smooth muscle in ducks with a vitamin
E-selenium deficiency.
J Nutr. 1975 Jun;105(6):782-90.
PMID: 167138 [PubMed - indexed for MEDLINE]

901: Pachter BR, Davidowitz J, Breinin GM.
Muscle fiber and motor end plate involvement in the extraocular muscles of the
myotonic mouse.
Invest Ophthalmol. 1975 Jun;14(6):418-27.
PMID: 166048 [PubMed - indexed for MEDLINE]

902: Kinoshita M, Satoyoshi E, Suzuki Y.
Atypical myopathy with myofibrillar aggregates.
Arch Neurol. 1975 Jun;32(6):417-20.
PMID: 165803 [PubMed - indexed for MEDLINE]

903: Inokuchi T, Umezaki H, Santa T.
A case of type 1 muscle fibre hypotrophy and internal nuclei.
J Neurol Neurosurg Psychiatry. 1975 May;38(5):475-82.
PMID: 168319 [PubMed - indexed for MEDLINE]

904: Lake BD, Wilson J.
Zebra body myopathy. Clinical, histochemical and ultrastructural studies.
J Neurol Sci. 1975 Apr;24(4):437-46.
PMID: 163896 [PubMed - indexed for MEDLINE]

905: Engel WK, Oberc MA.
Abundant nuclear rods in adult-onset rod disease.
J Neuropathol Exp Neurol. 1975 Mar;34(2):119-32.
PMID: 47386 [PubMed - indexed for MEDLINE]

906: Wisniewski HM, Berry K, Spiro AJ.
Ultrastructure of thalamic neuronal inclusions in myotonic dystrophy.
J Neurol Sci. 1975 Mar;24(3):321-9.
PMID: 46919 [PubMed - indexed for MEDLINE]

907: Stern LZ, Payne CM, Alvarez JT, Hannapel LK.
Myopathy associated with linear scleroderma. A histochemical and electron
microscopic study.
Neurology. 1975 Feb;25(2):114-9.
PMID: 163451 [PubMed - indexed for MEDLINE]

908: Cullen MJ, Fulthorpe JJ.
Stages in fibre breakdown in Duchenne muscular dystrophy. An
electron-microscopic study.
J Neurol Sci. 1975 Feb;24(2):179-200.
PMID: 163299 [PubMed - indexed for MEDLINE]

909: Fu Y, Ward J, Young HF.
Unusual, rod-shaped cytoplasmic inclusions (Hirano bodies) in a cerebellar
hemangioblastoma.
Acta Neuropathol (Berl). 1975;31(2):129-35.
PMID: 166545 [PubMed - indexed for MEDLINE]

910: McLeod JG, Baker Wde C, Shorey CD, Kerr CB.
Mitochondrial myopathy with multisystem abnormalities and normal ocular
movements.
J Neurol Sci. 1975 Jan;24(1):39-52. No abstract available.
PMID: 162937 [PubMed - indexed for MEDLINE]

911: Bloem JJ, Vuzevski VD, Huffstadt AJ.
Recurring digital fibroma of infancy.
J Bone Joint Surg Br. 1974 Nov;56-B(4):746-51. No abstract available.
PMID: 4452723 [PubMed - indexed for MEDLINE]

912: Sulaiman WR, Doyle D, Johnson RH, Jennett S.
Myopathy with mitochondrial inclusion bodies: histological and metabolic
studies.
J Neurol Neurosurg Psychiatry. 1974 Nov;37(11):1236-46. No abstract available.
PMID: 4376164 [PubMed - indexed for MEDLINE]

913: Dahl DS, Klutzow FW.
Congenital rod disease. Further evidence of innervational abnormalities as the
basis for the clinicopathologic features.
J Neurol Sci. 1974 Nov;23(3):371-85. No abstract available.
PMID: 4154364 [PubMed - indexed for MEDLINE]

914: Santavuori P, Haltia M, Rapola J.
Infantile type of so-called neuronal ceroid-lipofuscinosis.
Dev Med Child Neurol. 1974 Oct;16(5):644-53. No abstract available.
PMID: 4371326 [PubMed - indexed for MEDLINE]

915: Rose AG.
An electron microscopic study of the giant cells in proliferative myositis.
Cancer. 1974 Jun;33(6):1543-7. No abstract available.
PMID: 4365299 [PubMed - indexed for MEDLINE]

916: Rawles JM, Weller RO.
Familial association of metabolic myopathy, lactic acidosis and sideroblastic
anemia.
Am J Med. 1974 Jun;56(6):891-7. No abstract available.
PMID: 4364695 [PubMed - indexed for MEDLINE]

917: Gordon AS, Rewcastle NB, Humphrey JG, Stewart BM.
Chronic benign congenital myopathy: fingerprint body type.
Can J Neurol Sci. 1974 May;1(2):106-13. No abstract available.
PMID: 4373157 [PubMed - indexed for MEDLINE]

918: Morgan J, Cohen L.
Letter: Crystalline perinuclear inclusions in myoblasts from human dystrophic
muscle.
N Engl J Med. 1974 Apr 11;290(15):863. No abstract available.
PMID: 4361764 [PubMed - indexed for MEDLINE]

919: Berk SH, Blank H.
Ultraviolet light and cytoplasmic tubules in lupus erythematosus.
Arch Dermatol. 1974 Mar;109(3):364-6. No abstract available.
PMID: 4360831 [PubMed - indexed for MEDLINE]

920: Farkas E, Tome FM, Fardeau M, Arsenio-Nunes ML, Dreyfus P, Diebler MF.
Histochemical and ultrastructural study of muscle biopsies in 3 cases of
dystrophia myotonica in the newborn child.
J Neurol Sci. 1974 Mar;21(3):273-88. No abstract available.
PMID: 4150367 [PubMed - indexed for MEDLINE]

921: Julien J, Vital C, Vallat JM, Vallat M, Le Blanc M.
Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and
"fingerprint" inclusions.
J Neurol Sci. 1974 Feb;21(2):165-9. No abstract available.
PMID: 4374513 [PubMed - indexed for MEDLINE]

922: Martinez AJ, Hooshmand H, Mendoza GI, Winston YE.
Fatal polymyositis: morphogenesis and ultrastructural features.
Acta Neuropathol (Berl). 1974;29(3):251-62. No abstract available.
PMID: 4374860 [PubMed - indexed for MEDLINE]

923: Bastiaensen LA, Hommes OR, Stadhouders AM.
Ocular myopathy. A case history with electron microscopy, biochemistry and

review of literature.
Ophthalmologica. 1974;168(5):325-47. No abstract available.
PMID: 4364907 [PubMed - indexed for MEDLINE]

924: Martinez AJ, Hooshmand H, Faris AA.
Acute alcoholic myopathy. Enzyme histochemistry and electron microscopic
findings.
J Neurol Sci. 1973 Nov;20(3):245-52. No abstract available.
PMID: 4357768 [PubMed - indexed for MEDLINE]

925: Bonucci E, Derenzini M, Marinozzi V.
The organic-inorganic relationship in calcified mitochondria.
J Cell Biol. 1973 Oct;59(1):185-211. No abstract available.
PMID: 4127538 [PubMed - indexed for MEDLINE]

926: Defendini R, Markesbery WR, Mastri AR, Duffy PE.
Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Ultrastructural
observations, anatomical pathology and nosology.
J Neurol Sci. 1973 Sep;20(1):7-23. No abstract available.
PMID: 4355342 [PubMed - indexed for MEDLINE]

927: Culebras A, Feldman RG, Merk FB.
Cytoplasmic inclusion bodies within neurons of the thalamus in myotonic
dystrophy. A light and electron microscope study.
J Neurol Sci. 1973 Jul;19(3):319-29. No abstract available.
PMID: 4123799 [PubMed - indexed for MEDLINE]

928: Grrimley PM, Decker JL, Michelitch HJ, Frantz MM.
Abnormal structures in circulating lymphocytes from patients with systemic
lupus erythematosus and related diseases.
Arthritis Rheum. 1973 May-Jun;16(3):313-23. No abstract available.
PMID: 4708012 [PubMed - indexed for MEDLINE]

929: Sandbank U, Sroka H, Kuritzky A, Bornstein B.
Limb-girdle muscular dystrophy. Case report with electron microscopic study of
a muscle biopsy.
Isr J Med Sci. 1973 May;9(5):603-11. No abstract available.
PMID: 4352261 [PubMed - indexed for MEDLINE]

930: Schochet SS Jr, McCormick WF.
Polymyositis with intranuclear inclusions. A light and electron microscopic
study.
Arch Neurol. 1973 Apr;28(4):280-3. No abstract available.
PMID: 4347327 [PubMed - indexed for MEDLINE]

931: Tome FM, Fardeau M.
"Fingerprint inclusions" in muscle fibres in dystrophia myotonica.
Acta Neuropathol (Berl). 1973 Mar 30;24(1):62-7. No abstract available.
PMID: 4349378 [PubMed - indexed for MEDLINE]

932: Fidzianska A.
Virus-like structures in muscle in chronic polymyositis.
Acta Neuropathol (Berl). 1973;23(1):23-31. No abstract available.
PMID: 4698522 [PubMed - indexed for MEDLINE]

933: Kitano Y, Horiki M, Aoki T, Sagami S.
Two cases of juvenile hyalin fibromatosis. Some histological, electron
microscopic, and tissue culture observations.
Arch Dermatol. 1972 Dec;106(6):877-83. No abstract available.
PMID: 4118157 [PubMed - indexed for MEDLINE]

934: Ben-Bassat M, Machtey I.
Picornavirus-like structures in acute dermatomyositis.
Am J Clin Pathol. 1972 Sep;58(3):245-9. No abstract available.
PMID: 5075105 [PubMed - indexed for MEDLINE]

935: Pachter BR, Davidowitz J, Breinin GM.
A phase-electron microscopic study of extraocular muscle dystrophy in the
mouse.
Invest Ophthalmol. 1972 Sep;11(9):715-22. No abstract available.
PMID: 4340861 [PubMed - indexed for MEDLINE]

936: McMurtry SL, Julian LM, Asmundson VS.
Hereditary muscular dystrophy of the chicken. Quantitative histopathological
findings of the Pectoralis at 6 weeks of age.
Arch Pathol. 1972 Sep;94(3):217-24. No abstract available.
PMID: 4340660 [PubMed - indexed for MEDLINE]

937: Gyorkey F, Sinkovics JG, Min KW, Gyorkey P.
A morphologic study on the occurrence and distribution of structures resembling
viral nucleocapsids in collagen diseases.
Am J Med. 1972 Aug;53(2):148-58. No abstract available.
PMID: 5050548 [PubMed - indexed for MEDLINE]

938: Bove KE, Shelburne SA Jr.
Subacute inclusion body encephalitis associated with myopathy.
Arch Neurol. 1972 Jul;27(1):42-4. No abstract available.
PMID: 5049679 [PubMed - indexed for MEDLINE]

939: Landry M, Winkelmann RK.
Tubular cytoplasmic inclusion in dermatomyositis.
Mayo Clin Proc. 1972 Jul;47(7):479-92. No abstract available.
PMID: 4339202 [PubMed - indexed for MEDLINE]

940: Der Kaloustian VM, Afifi AK, Mire J.
The myopathic variety of arthrogryposis multiplex congenita: a disorder with
autosomal recessive inheritance.
J Pediatr. 1972 Jul;81(1):76-82. No abstract available.
PMID: 4338386 [PubMed - indexed for MEDLINE]

941: Engel AG, Angelini C, Gomez MR.
Fingerprint body myopathy, a newly recognized congenital muscle disease.
Mayo Clin Proc. 1972 Jun;47(6):377-88. No abstract available.
PMID: 4339422 [PubMed - indexed for MEDLINE]

942: Binette JP, Montes M, Lee JC.
Electron microscopy of muscle biopsies in two cases of meningococcemia.
J Med. 1972;3(2):88-96. No abstract available.
PMID: 4116400 [PubMed - indexed for MEDLINE]

943: Tisher CC, Kelso HB, Robinson RR, Gunnells JC, Burkholder PM.
Intraendothelial inclusions in kidneys of patients with systemic lupus
erythematosus.
Ann Intern Med. 1971 Oct;75(4):537-47. No abstract available.
PMID: 4398449 [PubMed - indexed for MEDLINE]

944: Yunis EJ, Samaha FJ.
Inclusion body myositis.
Lab Invest. 1971 Sep;25(3):240-8. No abstract available.
PMID: 5095321 [PubMed - indexed for MEDLINE]

945: Winchester RJ, Koffler D, Litwin SD, Kunkel HG.
Observations on the eosinophilia of certain patients with rheumatoid arthritis.
Arthritis Rheum. 1971 Sep-Oct;14(5):650-65. No abstract available.
PMID: 4328684 [PubMed - indexed for MEDLINE]

946: Sato T, Walker DL, Peters HA, Resse HH, Chou SM.
Chronic polymyositis and myxovirus-like inclusions. Electron microscopic and
viral studies.
Arch Neurol. 1971 May;24(5):409-18. No abstract available.
PMID: 4324435 [PubMed - indexed for MEDLINE]

947: Mastaglia FL, Walton JN.
An ultrastructural study of skeletal muscle in polymyositis.
J Neurol Sci. 1971 Apr;12(4):473-504. No abstract available.
PMID: 5572834 [PubMed - indexed for MEDLINE]

948: Hashimoto K, Robison L, Velayos E, Niizuma K.
Dermatomyositis. Electron microscopic, immunologic, and tissue culture studies
of paramyxovirus-like inclusions.
Arch Dermatol. 1971 Feb;103(2):120-35. No abstract available.
PMID: 4324055 [PubMed - indexed for MEDLINE]

949: Ionescu V, Radu H, Nicolescu P.
Ultrastructural changes in hypokalemic periodic paralysis.
Rev Roum Neurol. 1971;8(6):419-25. No abstract available.
PMID: 4334608 [PubMed - indexed for MEDLINE]

950: Mastaglia FL, Walton JN.
Coxsackie virus-like particles in skeletal muscle from a case of polymyositis.
J Neurol Sci. 1970 Dec;11(6):593-9. No abstract available.
PMID: 5490731 [PubMed - indexed for MEDLINE]

951: Carpenter S, Karpati G, Wolfe L.
Virus-like filaments and phospholipid accumulation in skeletal muscle. Study of
a histochemically distinct chronic myopathy.
Neurology. 1970 Sep;20(9):889-903. No abstract available.
PMID: 5466457 [PubMed - indexed for MEDLINE]

952: Feorino PM, Hierholzer JC, Norton WL.
Viral isolation studies of inclusion positive biopsy from human connective
tissue diseases.
Arthritis Rheum. 1970 Jul-Aug;13(4):378-80. No abstract available.
PMID: 4988023 [PubMed - indexed for MEDLINE]

953: Hashimoto K, Thompson DF.
Discoid lupus erythematosus. Electron microscopic studies of paramyxovirus-like
structures.
Arch Dermatol. 1970 May;101(5):565-7. No abstract available.
PMID: 5444077 [PubMed - indexed for MEDLINE]

954: Macdonald RD, Engel AG.
Structure and composition of nemaline rods: evidence that they represent
replicating Z disk.
Neurology. 1970 Apr;20(4):413-4. No abstract available.
PMID: 4327345 [PubMed - indexed for MEDLINE]

955: Vick NA.
Polymyositis: fine structure of capillaries and subcellular organelles.
Neurology. 1970 Apr;20(4):406. No abstract available.
PMID: 4327342 [PubMed - indexed for MEDLINE]

956: Norris FH Jr, Dramov B, Calder CD, Johnson SG.
Virus-like particles in myositis accompanying herpes zoster.
Arch Neurol. 1969 Jul;21(1):25-31. No abstract available.
PMID: 5772548 [PubMed - indexed for MEDLINE]

957: Schneider C, Gould WJ, Mirani R.
Granular cell myoblastoma of larynx. Two case reports.
Arch Otolaryngol. 1969 Jun;89(6):873-7. No abstract available.
PMID: 4306738 [PubMed - indexed for MEDLINE]

958: Sato T, Walker DL, Peters HA, Reese HH, Chou SM.
Myxovirus-like inclusion bodies in chronic polymyositis: Electron microscopic
and viral studies.
Trans Am Neurol Assoc. 1969;94:339-41. No abstract available.
PMID: 4190701 [PubMed - indexed for MEDLINE]

959: Chou SM.
Myxovirus-like structures and accompanying nuclear changes in chronic
polymyositis.
Arch Pathol. 1968 Dec;86(6):649-58. No abstract available.
PMID: 5701638 [PubMed - indexed for MEDLINE]

960: Kolin IS.
Nemaline myopathy. A fatal case.
Am J Dis Child. 1967 Jul;114(1):95-100. No abstract available.
PMID: 4378108 [PubMed - indexed for MEDLINE]

961: PRICE HM, HOWES EL Jr, BLUMBERG JM.
ULTRASTRUCTURAL ALTERATIONS IN SKELETAL MUSCLE FIBERS INJURED BY COLD. II.
CELLS ON THE SARCOLEMMAL TUBE: OBSERVATIONS ON "DISCONTINUOUS" REGENERATION AND
MYOFIBRIL FORMATION.
Lab Invest. 1964 Oct;13:1279-302. No abstract available.
PMID: 14217477 [PubMed - OLDMEDLINE for Pre1966]