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Neuromuscular Disorders : NMD|November 11, 2011
A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathologyMélissa Bowerman, Lyndsay M Murray, Ariane Beauvais, et al.
Neuromuscular Disorders : NMD|October 14, 2011
Cardiac and muscle imaging findings in a family with X-linked Emery-Dreifuss muscular dystrophyNicola Carboni, Marco Mura, Eugenio Mercuri, et al.
Neuromuscular Disorders : NMD|August 9, 2011
Amyloidosis and exercise intolerance in ANO5 muscular dystrophyMargherita Milone, Teerin Liewluck, Thomas L Winder, et al.
Neuromuscular Disorders : NMD|July 6, 2011
Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathiesS Vuillaumier-Barrot, C Bouchet-Seraphin, M Chelbi, et al.
Neuromuscular Disorders : NMD|September 17, 2011
A novel CRYAB mutation resulting in multisystemic diseaseSabrina Sacconi, Léonard Féasson, Jean Christophe Antoine, et al.
Neuromuscular Disorders : NMD|August 3, 2011
Relationships of thigh muscle contractile and non-contractile tissue with function, strength, and age in boys with Duchenne muscular dystrophyHiroshi Akima, Donovan Lott, Claudia Senesac, et al.
Neuromuscular Disorders : NMD|January 24, 2012
Cardiac dysfunction and pathology in the dystrophin and utrophin-deficient mouse during development of dilated cardiomyopathyJu Lan Chun, Robert O'Brien, Suzanne E Berry
Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
Neuromuscular Disorders : NMD|December 14, 2011
Endpoint measures in the mdx mouse relevant for muscular dystrophy pre-clinical studiesYvonne M Kobayashi, Erik P Rader, Robert W Crawford, et al.
Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.
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