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Neuromuscular Disorders : NMD|December 11, 2020
Early onset neutral lipid storage disease with myopathy presenting as congenital hypotonia and hepatomegalyDaniela Avila-Smirnow, Gloria Durán-Saavedra, Pilar Ovalle-Besa, et al.Neuromuscular Disorders : NMD|January 29, 2021
Characterization of cannabis use by patients with myotonic dystrophy type 1: A pilot studyWilliam Beauchesne, Catherine Savard, Marika Côté-Hamel, et al.Neuromuscular Disorders : NMD|January 17, 2021
Feeding difficulties in children and adolescents with spinal muscular atrophy type 2Renske I Wadman, Ramona De Amicis, Chiara Brusa, et al.Neuromuscular Disorders : NMD|November 16, 2021
Predictors of outcome in patients with myasthenic crisis undergoing non-invasive mechanical ventilation: A retrospective 20 year longitudinal cohort study from a single Italian centerErika Iori, Marco Mazzoli, Alessandra Ariatti, et al.Neuromuscular Disorders : NMD|March 8, 2021
Disease-modifying effects of edasalonexent, an NF-κB inhibitor, in young boys with Duchenne muscular dystrophy: Results of the MoveDMD phase 2 and open label extension trialRichard S Finkel, Erika Finanger, Krista Vandenborne, et al.Neuromuscular Disorders : NMD|November 5, 2021
X-linked myotubular myopathyMichael W Lawlor, James J DowlingNeuromuscular Disorders : NMD|November 5, 2021
Two decades of advances in muscle imaging in children: from pattern recognition of muscle diseases to quantification and machine learning approachesDavid Gómez-Andrés, Amal Oulhissane, Susana Quijano-RoyNeuromuscular Disorders : NMD|November 5, 2021
Congenital myasthenic syndromes: where do we go from here?Sithara Ramdas, David BeesonNeuromuscular Disorders : NMD|November 5, 2021
Spinal muscular atrophy: from rags to richesEugenio MercuriNeuromuscular Disorders : NMD|November 6, 2021
Variant transthyretin amyloidosis (ATTRv) polyneuropathy in Greece: a broad overview with a focus on non-endemic unexplored regions of the countryGeorgios Koutsis, Efstathios Kastritis, Zoi Kontogeorgiou, et al.Pageof 340