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Neuromuscular Disorders : NMD|March 20, 2021
Filling the gaps in knowledge translation: Physical therapy recommendations for individuals with spinal muscular atrophy compared to standard of care guidelinesJessica Trenkle, Jessica Brugman, Anne Peterson, et al.Neuromuscular Disorders : NMD|November 5, 2021
The DMD gene and therapeutic approaches to restore dystrophinFernanda Fortunato, Marianna Farnè, Alessandra FerliniNeuromuscular 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 ReillyNeuromuscular Disorders : NMD|November 5, 2021
Genetic neuromuscular disorders: what is the best that we can do?Nigel G Laing, Royston W Ong, Gianina RavenscroftNeuromuscular 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 11, 2019
Respiratory and upper limb function as outcome measures in ambulant and non-ambulant subjects with Duchenne muscular dystrophy: A prospective multicentre studyV Ricotti, V Selby, D Ridout, et al.Neuromuscular Disorders : NMD|March 31, 2019
Are novel outcome measures for Charcot-Marie-Tooth disease sensitive to change? The 6-minute walk test and StepWatch™ Activity Monitor in a 12-month longitudinal studyCostanza Pazzaglia, Luca Padua, Davide Pareyson, 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.Pageof 341