134 related articles for article (PubMed ID: 9847994)
21. Sporadic Inclusion Body Myositis and Other Rimmed Vacuolar Myopathies.
Weihl CC
Continuum (Minneap Minn); 2019 Dec; 25(6):1586-1598. PubMed ID: 31794461
[TBL] [Abstract][Full Text] [Related]
22. Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis.
Askanas V; Engel WK
Curr Opin Rheumatol; 1998 Nov; 10(6):530-42. PubMed ID: 9812213
[TBL] [Abstract][Full Text] [Related]
23. Intranuclear and cytoplasmic filamentous inclusions in distal myopathy (Welander).
Borg K; Tomé FM; Edström L
Acta Neuropathol; 1991; 82(2):102-6. PubMed ID: 1656692
[TBL] [Abstract][Full Text] [Related]
24. 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.
Askanas V; Engel WK; Yang CC; Alvarez RB; Lee VM; Wisniewski T
Am J Pathol; 1998 Apr; 152(4):889-95. PubMed ID: 9546349
[TBL] [Abstract][Full Text] [Related]
25. New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies.
Askanas V; Engel WK
Curr Opin Rheumatol; 1995 Nov; 7(6):486-96. PubMed ID: 8579968
[TBL] [Abstract][Full Text] [Related]
26. The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype.
Rojana-udomsart A; Needham M; Luo YB; Fabian V; Walters S; Zilko PJ; Mastaglia FL
Clin Neurol Neurosurg; 2011 Sep; 113(7):559-63. PubMed ID: 21507567
[TBL] [Abstract][Full Text] [Related]
27. Autophagy in a mouse model of distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
Malicdan MC; Noguchi S; Nishino I
Autophagy; 2007; 3(4):396-8. PubMed ID: 17471014
[TBL] [Abstract][Full Text] [Related]
28. [Distal myopathy with rimmed vacuoles(DMRV)].
Ikeuchi T; Tsuji S
Nihon Rinsho; 1997 Dec; 55(12):3195-9. PubMed ID: 9436435
[TBL] [Abstract][Full Text] [Related]
29. Recent advances in distal myopathy with rimmed vacuoles (DMRV) or hIBM: treatment perspectives.
Malicdan MC; Noguchi S; Nishino I
Curr Opin Neurol; 2008 Oct; 21(5):596-600. PubMed ID: 18769255
[TBL] [Abstract][Full Text] [Related]
30. Ubiquitin immunostaining and inclusion body myositis: study of 30 patients with inclusion body myositis.
Prayson RA; Cohen ML
Hum Pathol; 1997 Aug; 28(8):887-92. PubMed ID: 9269823
[TBL] [Abstract][Full Text] [Related]
31. Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology.
Fidziańska A; Rowińska-Marcińska K; Hausmanowa-Petrusewicz I
Acta Neuropathol; 2004 Mar; 107(3):197-203. PubMed ID: 14712398
[TBL] [Abstract][Full Text] [Related]
32. Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis.
Weihl CC; Baloh RH; Lee Y; Chou TF; Pittman SK; Lopate G; Allred P; Jockel-Balsarotti J; Pestronk A; Harms MB
Neuromuscul Disord; 2015 Apr; 25(4):289-96. PubMed ID: 25617006
[TBL] [Abstract][Full Text] [Related]
33. Inclusion-body myositis and myopathies: different etiologies, possibly similar pathogenic mechanisms.
Askanas V; Engel WK
Curr Opin Neurol; 2002 Oct; 15(5):525-31. PubMed ID: 12351995
[TBL] [Abstract][Full Text] [Related]
34. Clinical assessment determines the diagnosis of inclusion body myositis independently of pathological features.
Brady S; Squier W; Hilton-Jones D
J Neurol Neurosurg Psychiatry; 2013 Nov; 84(11):1240-6. PubMed ID: 23864699
[TBL] [Abstract][Full Text] [Related]
35. Distal myopathies.
Nonaka I
Curr Opin Neurol; 1999 Oct; 12(5):493-9. PubMed ID: 10590885
[TBL] [Abstract][Full Text] [Related]
36. An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families.
Sivakumar K; Semino-Mora C; Dalakas MC
Brain; 1997 Apr; 120 ( Pt 4)():653-61. PubMed ID: 9153127
[TBL] [Abstract][Full Text] [Related]
37. Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.
Jansson M; Darin N; Kyllerman M; Martinsson T; Wahlström J; Oldfors A
Acta Neuropathol; 2000 Jul; 100(1):23-8. PubMed ID: 10912916
[TBL] [Abstract][Full Text] [Related]
38. Inclusion body myositis: current pathogenetic concepts and diagnostic and therapeutic approaches.
Needham M; Mastaglia FL
Lancet Neurol; 2007 Jul; 6(7):620-31. PubMed ID: 17582362
[TBL] [Abstract][Full Text] [Related]
39. Expression of the lysosome-associated membrane proteins in myopathies with rimmed vacuoles.
Tsuruta Y; Furuta A; Furuta K; Yamada T; Kira J; Iwaki T
Acta Neuropathol; 2001 Jun; 101(6):579-84. PubMed ID: 11515786
[TBL] [Abstract][Full Text] [Related]
40. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
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
Nat Genet; 2001 Sep; 29(1):83-7. PubMed ID: 11528398
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
