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Neuromuscular Disorders : NMD|December 10, 2013
Diaphragmatic dysfunction in Collagen VI myopathiesS Quijano-Roy, S Khirani, M Colella, et al.Neuromuscular Disorders : NMD|December 11, 2013
Pharmacokinetics and safety of single doses of drisapersen in non-ambulant subjects with Duchenne muscular dystrophy: results of a double-blind randomized clinical trialKevin M Flanigan, Thomas Voit, Xiomara Q Rosales, et al.Neuromuscular Disorders : NMD|October 10, 2013
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptomsF L Mastaglia, A Rojana-udomsart, I James, et al.Neuromuscular Disorders : NMD|October 17, 2013
Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2Satomi Mitsuhashi, Steven E Boyden, Elicia A Estrella, et al.Neuromuscular Disorders : NMD|May 29, 2012
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic deliveryStella Mitrani-Rosenbaum, Lena Yakovlev, Michal Becker Cohen, et al.Neuromuscular Disorders : NMD|June 1, 1997
Welander distal myopathy is not linked to other defined distal myopathy gene lociG Ahlberg, K Borg, L Edström, et al.Neuromuscular Disorders : NMD|May 1, 1997
Mitochondrial tRNA(Cys) gene mutation (A5814G): a second family with mitochondrial encephalopathyF M Santorelli, G Siciliano, C Casali, et al.Neuromuscular Disorders : NMD|May 1, 1997
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chainC A Sewry, I Naom, M D'Alessandro, et al.Neuromuscular Disorders : NMD|July 1, 1993
Development of electrical myotonia in the ADR mouse: role of chloride conductance in myotubes and neonatal animalsE Wischmeyer, E Nolte, R Klocke, et al.Pageof 341