Phenotypic heterogeneity in familial inclusion body myopathy
- 1 May 1995
- journal article
- case report
- Published by Wiley in Muscle & Nerve
- Vol. 18 (5) , 546-548
- https://doi.org/10.1002/mus.880180512
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Inclusion Body Myositis: New ConceptsSeminars in Neurology, 1993
- Vacuolar myopathy sparing the quadricepsBrain, 1993
- Polymyositis, Dermatomyositis, and Inclusion-Body MyositisNew England Journal of Medicine, 1991
- Inclusion body myositis and welander distal myopathy: a clinical, neurophysiological and morphological comparisonJournal of the Neurological Sciences, 1991
- Familial Inclusion Body Myositis Among Kurdish-Iranian JewsArchives of Neurology, 1991
- Presence of inclusion body myositis‐like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 casesNeuropathology and Applied Neurobiology, 1990
- INCLUSION BODY MYOSITISBrain, 1989
- DISTAL MYOPATHY WITH RIMMED VACUOLE FORMATIONBrain, 1989
- Adult‐onset autosomal dominant limb‐girdle muscular dystrophyAnnals of Neurology, 1986
- “Rimmed vacuole myopathy” sparing the quadriceps: A unique disorder in iranian jewsJournal of the Neurological Sciences, 1984