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Neuromuscular Disorders : NMD|May 11, 2007
Managing Duchenne muscular dystrophy--the additive effect of spinal surgery and home nocturnal ventilation in improving survivalMichelle Eagle, John Bourke, Robert Bullock, et al.Neuromuscular Disorders : NMD|October 2, 2009
Myopathy secondary to intravascular large B-cell lymphomaC Marini-Bettolo, R Lane, P Charles, et al.Neuromuscular Disorders : NMD|October 2, 2009
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophyKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.Neuromuscular Disorders : NMD|June 23, 2009
Muscle ultrasound measurements and functional muscle parameters in non-dystrophic myotonias suggest structural muscle changesJ Trip, S Pillen, C G Faber, et al.Neuromuscular Disorders : NMD|June 23, 2009
Hereditary motor and sensory neuropathy caused by a novel mutation in LITAFWanda Maria Gerding, Judith Koetting, Jörg Thomas Epplen, et al.Neuromuscular Disorders : NMD|September 24, 2009
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 geneMichela Catteruccia, Tommaso Sanna, Filippo Maria Santorelli, et al.Neuromuscular Disorders : NMD|July 21, 2009
Dysphagia in X-linked bulbospinal muscular atrophy (Kennedy disease)Tobias Warnecke, Stephan Oelenberg, Inga Teismann, et al.Neuromuscular Disorders : NMD|August 21, 2009
What we do not know about pregnancy in hereditary neuromuscular disordersZohar Argov, Marianne de VisserNeuromuscular Disorders : NMD|August 24, 2010
Clinical and neuropathological findings in patients with TACO1 mutationsJürgen Seeger, Bertold Schrank, Angela Pyle, et al.Neuromuscular Disorders : NMD|April 2, 2010
Episodic myoglobinuria in a primary gamma-sarcoglycanopathyLoren Pena, Katherine Kim, Joel CharrowPageof 340