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Neuromuscular Disorders : NMD|November 5, 2021
The DMD gene and therapeutic approaches to restore dystrophinFernanda Fortunato, Marianna Farnè, Alessandra Ferlini
Neuromuscular Disorders : NMD|November 5, 2021
Inflammatory myopathies in childhoodWerner Stenzel, Hans-Hilmar Goebel, Brigitte Bader-Meunier, et al.
Neuromuscular Disorders : NMD|November 5, 2021
Neurogenic arthrogryposis and the power of phenotypingAlexander M Rossor, Mary M Reilly
Neuromuscular Disorders : NMD|November 5, 2021
Genetic neuromuscular disorders: what is the best that we can do?Nigel G Laing, Royston W Ong, Gianina Ravenscroft
Neuromuscular Disorders : NMD|February 17, 2019
Reevaluating the pathogenicity of the mutation c.1194 +5 G>A in GAA gene by functional analysis of RNA in a 61-year-old woman diagnosed with Pompe disease by muscle biopsyCinthia Amiñoso, María Gordillo-Marañón, Jaime Hernández, et al.
Neuromuscular Disorders : NMD|March 10, 2019
Mitochondrial DNA depletion in sporadic inclusion body myositisPadmanabh S Bhatt, Charalampos Tzoulis, Novin Balafkan, et al.
Neuromuscular Disorders : NMD|March 23, 2019
Cardiac autonomic function evaluation in pediatric and adult patients with congenital myasthenic syndromesCeren Günbey, Kutay Sel, Çağrı Mesut Temuçin, et al.
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