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Annals of Neurology|April 1, 2003
Phenotypic spectrum associated with mutations in the fukutin-related protein geneEugenio Mercuri, Martin Brockington, Volker Straub, et al.Brain : a Journal of Neurology|October 14, 2011
Long-term observational study of sporadic inclusion body myositisOlivier Benveniste, Marguerite Guiguet, Jane Freebody, et al.Neuromuscular Disorders : NMD|March 8, 2016
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcomeKarim Wahbi, Frederic A Sebag, Nicolas Lellouche, et al.Neuromuscular Disorders : NMD|September 18, 2007
Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathiesHiroshi Manya, Céline Bouchet, Akiko Yanagisawa, et al.Acta Neuropathologica Communications|January 29, 2015
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravisMarie Maurer, Sylvain Bougoin, Tali Feferman, et al.Annals of Neurology|July 12, 2002
Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13Louis Viollet, Annie Barois, Jean G Rebeiz, et al.Journal of Neuromuscular Diseases|June 6, 2018
Efficacy of Rituximab in Refractory Generalized anti-AChR Myasthenia GravisOcéane Landon-Cardinal, Diane Friedman, Marguerite Guiguet, et al.Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.Human Mutation|February 7, 2008
Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with coresNicole Monnier, Isabelle Marty, Julien Faure, et al.Journal of Neuromuscular Diseases|November 19, 2016
Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related DiseasesIsabelle Nelson, Tanya Stojkovic, Valérie Allamand, et al.Pageof 26