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Neuromuscular Disorders : NMD|September 8, 2004
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouseAlexandre Briguet, Isabelle Courdier-Fruh, Mark Foster, et al.Neuromuscular Disorders : NMD|September 13, 2016
Novel mutation in TCAP manifesting with asymmetric calves and early-onset joint retractionsCarlos Pablo de Fuenmayor-Fernández de la Hoz, Aurelio Hernández-Laín, Montse Olivé, et al.Neuromuscular Disorders : NMD|September 13, 2016
Mitochondrial dysfunction in myofibrillar myopathyAmy E Vincent, John P Grady, Mariana C Rocha, et al.Neuromuscular Disorders : NMD|September 13, 2016
Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutationYi Shiau Ng, Steven A Hardy, Venice Shrier, et al.Neuromuscular Disorders : NMD|September 12, 2016
Effective cauda equina decompression in two siblings with Charcot-Marie-Tooth disease type 1BTristan P C van Doormaal, Fred van Ruissen, Kai J Miller, et al.Neuromuscular Disorders : NMD|September 18, 2016
SWORD: A simplified desensitization protocol for enzyme replacement therapy in adult Pompe diseaseLaure Gallay, Philippe Petiot, Isabelle Durieu, et al.Neuromuscular Disorders : NMD|June 25, 2017
Associations between timing of corticosteroid treatment initiation and clinical outcomes in Duchenne muscular dystrophySunkyung Kim, Yong Zhu, Paul A Romitti, et al.Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.Neuromuscular Disorders : NMD|June 19, 2017
Muscle pathology in Vici syndrome-A case study with a novel mutation in EPG5 and a summary of the literatureCarola Hedberg-Oldfors, Niklas Darin, Anders OldforsNeuromuscular Disorders : NMD|February 26, 2010
Centronuclear myopathies: a widening conceptNorma Beatriz RomeroPageof 340