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Neurology|December 30, 2004
Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositisU A Badrising, G M Th Schreuder, M J Giphart, et al.
European Journal of Neurology|May 12, 2015
RYR1-related myopathies: a wide spectrum of phenotypes throughout lifeM Snoeck, B G M van Engelen, B Küsters, et al.
American Journal of Human Genetics|May 20, 1999
Calpainopathy-a survey of mutations and polymorphismsI Richard, C Roudaut, A Saenz, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Neuromuscular Disorders : NMD|July 2, 2013
Six minute walk test in type III spinal muscular atrophy: a 12month longitudinal studyE Mazzone, F Bianco, M Main, et al.
Evolutionary Applications|January 26, 2023
Towards evolutionary predictions: Current promises and challengesMeike T Wortel, Deepa Agashe, Susan F Bailey, et al.
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