158 related articles for article (PubMed ID: 8117535)
1. New advances in inclusion-body myositis.
Askanas V; Engel WK
Curr Opin Rheumatol; 1993 Nov; 5(6):732-41. PubMed ID: 8117535
[TBL] [Abstract][Full Text] [Related]
2. Idiopathic inflammatory myopathies: inclusion-body myositis, polymyositis, and dermatomyositis.
Askanas V; Engel WK; Mirabella M
Curr Opin Neurol; 1994 Oct; 7(5):448-56. PubMed ID: 7804466
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Strong immunoreactivity of alpha 1-antichymotrypsin co-localizes with beta-amyloid protein and ubiquitin in vacuolated muscle fibers of inclusion-body myositis.
Bilak M; Askanas V; Engel WK
Acta Neuropathol; 1993; 85(4):378-82. PubMed ID: 8386897
[TBL] [Abstract][Full Text] [Related]
5. Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau.
Askanas V; Engel WK; Bilak M; Alvarez RB; Selkoe DJ
Am J Pathol; 1994 Jan; 144(1):177-87. PubMed ID: 8291607
[TBL] [Abstract][Full Text] [Related]
6. Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy.
Sarkozi E; Askanas V; Engel WK
Am J Pathol; 1994 Dec; 145(6):1280-4. PubMed ID: 7992832
[TBL] [Abstract][Full Text] [Related]
7. Prion protein is abnormally accumulated in inclusion-body myositis.
Askanas V; Bilak M; Engel WK; Alvarez RB; Tomé F; Leclerc A
Neuroreport; 1993 Oct; 5(1):25-8. PubMed ID: 8280854
[TBL] [Abstract][Full Text] [Related]
8. beta-Amyloid precursor epitopes in muscle fibers of inclusion body myositis.
Askanas V; Alvarez RB; Engel WK
Ann Neurol; 1993 Oct; 34(4):551-60. PubMed ID: 7692809
[TBL] [Abstract][Full Text] [Related]
9. Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments.
Mendell JR; Sahenk Z; Gales T; Paul L
Arch Neurol; 1991 Dec; 48(12):1229-34. PubMed ID: 1668977
[TBL] [Abstract][Full Text] [Related]
10. Nitric oxide stress in sporadic inclusion body myositis muscle fibres: inhibition of inducible nitric oxide synthase prevents interleukin-1β-induced accumulation of β-amyloid and cell death.
Schmidt J; Barthel K; Zschüntzsch J; Muth IE; Swindle EJ; Hombach A; Sehmisch S; Wrede A; Lühder F; Gold R; Dalakas MC
Brain; 2012 Apr; 135(Pt 4):1102-14. PubMed ID: 22436237
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Sporadic inclusion-body myositis and its similarities to Alzheimer disease brain. Recent approaches to diagnosis and pathogenesis, and relation to aging.
Askanas V; Engel WK
Scand J Rheumatol; 1998; 27(6):389-405. PubMed ID: 9855208
[TBL] [Abstract][Full Text] [Related]
13. Myofibrillar myopathy with abnormal foci of desmin positivity. II. Immunocytochemical analysis reveals accumulation of multiple other proteins.
De Bleecker JL; Engel AG; Ertl BB
J Neuropathol Exp Neurol; 1996 May; 55(5):563-77. PubMed ID: 8627347
[TBL] [Abstract][Full Text] [Related]
14. Proposed pathogenetic cascade of inclusion-body myositis: importance of amyloid-beta, misfolded proteins, predisposing genes, and aging.
Askanas V; Engel WK
Curr Opin Rheumatol; 2003 Nov; 15(6):737-44. PubMed ID: 14569203
[TBL] [Abstract][Full Text] [Related]
15. Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis.
Askanas V; Engel WK; Alvarez RB
Am J Pathol; 1992 Jul; 141(1):31-6. PubMed ID: 1321564
[TBL] [Abstract][Full Text] [Related]
16. 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.
Semino-Mora C; Dalakas MC
Hum Pathol; 1998 Oct; 29(10):1128-33. PubMed ID: 9781653
[TBL] [Abstract][Full Text] [Related]
17. [Inclusion body myositis].
Serratrice G
Presse Med; 1996 Jun; 25(21):985-8. PubMed ID: 8692777
[TBL] [Abstract][Full Text] [Related]
18. Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies.
Mirabella M; Alvarez RB; Bilak M; Engel WK; Askanas V
J Neuropathol Exp Neurol; 1996 Jul; 55(7):774-86. PubMed ID: 8965093
[TBL] [Abstract][Full Text] [Related]
19. [Histological data in inflammatory myositis].
Mikol J; Polivka M
Ann Med Interne (Paris); 2001 Nov; 152(7):465-79. PubMed ID: 11965088
[TBL] [Abstract][Full Text] [Related]
20. beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle.
Sarkozi E; Askanas V; Johnson SA; Engel WK; Alvarez RB
Neuroreport; 1993 Jun; 4(6):815-8. PubMed ID: 8394158
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]