Results 171 to 174 of about 2,813 (174)

ActiMyo home monitoring in adult patients with limb girdle muscular dystrophy type 2B and facioscapulohumeral muscular dystrophy in study ATYR 1940-C-004

Neuromuscular Disorders, 2017
T. Gidaro, A. Moraux, M. Grelet, E. Gasnier, M. Villeret, M. Annoussamy, J. Vissing, S. Attarian, T. Mozaffar, S. Iyadurai, K. Wagner, G. Walker, A. Richiardi, S. Shukla, D. Vissière, L. Servais   +15 more
openaire   +1 more source

Limb–girdle muscular dystrophy: Diagnostic evaluation, frequency and clues to pathogenesis

Neuromuscular Disorders, 2008
Harriet P Lo, Sandra T Cooper, Frances J Evesson   +2 more
exaly  

Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy

Frontiers in Neurology
Claudia Cinnante, Stefania Corti, Giacomo P Comi   +2 more
exaly  

Variants in CAPN3 Causing Autosomal Dominant Limb–Girdle Muscular Dystrophy Combined With Calpain‐3 Deficiency

Human Mutation
Thomas Krag, Lauren Brady, Camille Verebi   +2 more
exaly