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Neuromuscular Disorders : NMD|August 1, 2015
Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot-Marie-Tooth diseaseKathryn M Brennan, Yunhong Bai, Chiara Pisciotta, et al.
Neuromuscular Disorders : NMD|December 18, 2013
Early infantile sensory-motor neuropathy with late onset respiratory distressAstrid Blaschek, Dieter Gläser, Marius Kuhn, et al.
Neuromuscular Disorders : NMD|June 19, 2017
Insights from genotype-phenotype correlations by novel SPEG mutations causing centronuclear myopathyHaicui Wang, Claudia Castiglioni, Ayşe Kaçar Bayram, et al.
Neuromuscular Disorders : NMD|June 19, 2017
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domainsElizabeth Harris, Umar Burki, Chiara Marini-Bettolo, et al.
Neuromuscular Disorders : NMD|June 14, 2017
Clinical, histological and radiological responses to methylprednisolone in HIV-associated rod myopathyAndré M S Silva, Rodrigo H Mendonça, Cristiane A M Moreno, et al.
Neuromuscular Disorders : NMD|July 14, 2018
Charcot-Marie-Tooth disease type 4C in Norway: Clinical characteristics, mutation spectrum and minimum prevalenceKjell Arne Arntzen, Helle Høyer, Kristin Ørstavik, et al.
Neuromuscular Disorders : NMD|November 18, 2005
The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase DeficiencyN C Voermans, P J Poels, L A Kluijtmans, et al.
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