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Neuromuscular Disorders : NMD|October 17, 2003
Detection of glucocorticoid-like activity in traditional Chinese medicine used for the treatment of Duchenne muscular dystrophyIsabelle Courdier-Fruh, Lee Barman, Philipp Wettstein, et al.Neuromuscular Disorders : NMD|October 17, 2003
Sexual differences in onset of disease and response to exercise in a transgenic model of ALSJ H Veldink, P R Bär, E A J Joosten, et al.Neuromuscular Disorders : NMD|October 17, 2003
Comparison of maximal voluntary isometric contraction and hand-held dynamometry in measuring muscle strength of patients with progressive lower motor neuron syndromeJ Visser, E Mans, M de Visser, et al.Neuromuscular Disorders : NMD|September 26, 2008
Sarcoidosis in a case of MuSK-positive myasthenia gravisKonstantinos Spengos, Sofia Vassilopoulou, Yiolanda Christou, et al.Neuromuscular Disorders : NMD|September 27, 2008
The relationship between regional body composition and quantitative strength in facioscapulohumeral muscular dystrophy (FSHD)Andrew J Skalsky, Richard T Abresch, Jay J Han, et al.Neuromuscular Disorders : NMD|July 8, 2008
Gastrointestinal involvement is frequent in Myotonic Dystrophy type 2Alide A Tieleman, Judith van Vliet, Jan B M J Jansen, et al.Neuromuscular Disorders : NMD|September 18, 2007
Reliability and feasibility of the six minute walk test in subjects with myotonic dystrophyMarie Kierkegaard, Anna TollbäckNeuromuscular Disorders : NMD|September 18, 2007
Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathiesHiroshi Manya, Céline Bouchet, Akiko Yanagisawa, et al.Neuromuscular Disorders : NMD|September 28, 2007
Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesisHarriet P Lo, Sandra T Cooper, Frances J Evesson, et al.Neuromuscular Disorders : NMD|August 1, 2008
A novel PYGM mutation in a Korean patient with McArdle disease: the role of nonsense-mediated mRNA decayEun Hee Sohn, Hyang-Sook Kim, Ae Young Lee, et al.Pageof 340