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Neuromuscular Disorders : NMD|July 23, 2019
The nature of respiratory muscle weakness in patients with late-onset Pompe diseaseJens Spiesshoefer, Carolin Henke, Hans Joachim Kabitz, et al.Neuromuscular Disorders : NMD|November 19, 2013
Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutationIzaskun Yurrebaso, Oscar L Casado, Joseba Barcena, et al.Neuromuscular Disorders : NMD|August 21, 2014
Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2Rosanna Cardani, Marzia Giagnacovo, Giulia Rossi, et al.Neuromuscular Disorders : NMD|September 4, 2014
Atypical presentation of GNE myopathy with asymmetric hand weaknessJohn Karl L de Dios, Joseph A Shrader, Galen O Joe, et al.Neuromuscular Disorders : NMD|October 5, 2015
The R900S mutation in CACNA1S associated with hypokalemic periodic paralysisQing Ke, Fangping He, Lingping Lu, et al.Neuromuscular Disorders : NMD|October 23, 2013
Novel mutations in the fukutin gene in a boy with asymptomatic hyperCKemiaChiara Fiorillo, Francesca Moro, Guja Astrea, et al.Neuromuscular Disorders : NMD|November 18, 2011
SETX gene mutation in a family diagnosed autosomal dominant proximal spinal muscular atrophySabine Rudnik-Schöneborn, Larissa Arning, Jörg T Epplen, et al.Neuromuscular Disorders : NMD|November 18, 2011
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutationsI Wargon, P Richard, T Kuntzer, et al.Neuromuscular Disorders : NMD|June 1, 2012
Cytochrome c oxidase-intermediate fibres: importance in understanding the pathogenesis and treatment of mitochondrial myopathyJulie L Murphy, Thiloka E Ratnaike, Ersong Shang, et al.Neuromuscular Disorders : NMD|June 2, 2012
Compound heterozygosity in a South African patient with facioscapulohumeral muscular dystrophyAntonel Olckers, Annelize van der Merwe, G Wayne Towers, et al.Pageof 340