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Neuromuscular Disorders : NMD|June 23, 2015
Quantitative muscle MRI: A powerful surrogate outcome measure in Duchenne muscular dystrophyUlrike Bonati, Patricia Hafner, Sabine Schädelin, et al.
Neuromuscular Disorders : NMD|November 5, 1997
Changes of laminin beta 2 chain expression in congenital muscular dystrophyR D Cohn, R Herrmann, U M Wewer, et al.
Neuromuscular Disorders : NMD|November 5, 1997
Association of genetically proven deficiencies of myophosphorylase and AMP deaminase: a second case of 'double trouble'J C Rubio, M A Martín, J Bautista, et al.
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 Parks
Neuromuscular 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 Wishart
Neuromuscular 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.
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