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Neuromuscular Disorders : NMD|July 28, 2016
Sport activity in Charcot-Marie-Tooth disease: A case study of a Paralympic swimmerGiuseppe Vita, Stefania La Foresta, Massimo Russo, et al.Neuromuscular Disorders : NMD|July 28, 2016
Opening the window: The case for carrier and perinatal screening for spinal muscular atrophyJoseph K Burns, Rashmi Kothary, Robin J ParksNeuromuscular Disorders : NMD|July 28, 2016
Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophyHeidi R Fuller, Thomas H Gillingwater, Thomas M WishartNeuromuscular Disorders : NMD|July 28, 2016
Cross-sectional retrospective study of muscle function in patients with glycogen storage disease type IIIValérie Decostre, Pascal Laforêt, Aleksandra Nadaj-Pakleza, et al.Neuromuscular Disorders : NMD|April 26, 2020
Expanding the disease phenotype of ADSSL1-associated myopathy in non-Korean patientsMagdalena Mroczek, Hacer Durmus, Sunita Bijarnia-Mahay, et al.Neuromuscular Disorders : NMD|April 25, 2020
Facioscapulohumeral muscular dystrophy 1 patients participating in the UK FSHD registry can be subdivided into 4 patterns of self-reported symptomsChristopher R S Banerji, Phillip Cammish, Teresinha Evangelista, et al.Neuromuscular Disorders : NMD|April 25, 2020
"Status myotonicus" in Nav1.4-M1592V channelopathyTorge Rempe, S H SubramonyNeuromuscular Disorders : NMD|January 1, 1992
Acute myopathy with selective degeneration of myosin filaments following status asthmaticus treated with methylprednisolone and vecuroniumA J Waclawik, R L Sufit, B R Beinlich, et al.Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.Neuromuscular Disorders : NMD|March 1, 2003
Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant miceL T Guo, X U Zhang, W Kuang, et al.Pageof 340