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Neuromuscular Disorders : NMD|May 28, 2008
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathyGiuliana Galassi, Eleonora Lamantea, Federica Invernizzi, et al.Neuromuscular Disorders : NMD|May 28, 2008
Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathiesKatharina Strach, Torsten Sommer, Christian Grohé, et al.Neuromuscular Disorders : NMD|May 28, 2008
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B geneBelén Bornstein, Estela Area, Kevin M Flanigan, et al.Neuromuscular Disorders : NMD|February 8, 2017
Comparison of ambulatory capacity and disease progression of Duchenne muscular dystrophy subjects enrolled in the drisapersen DMD114673 study with a matched natural history cohort of subjects on daily corticosteroidsNathalie Goemans, Mar Tulinius, Anna-Karin Kroksmark, et al.Neuromuscular Disorders : NMD|February 4, 2017
Prognostic value of nocturnal hypoventilation in neuromuscular patientsDavid Orlikowski, Helene Prigent, Maria-Antonia Quera Salva, et al.Neuromuscular Disorders : NMD|January 10, 2017
Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasisElena Campione, Annalisa Botta, Monia Di Prete, et al.Neuromuscular Disorders : NMD|February 5, 2017
The role of p62/SQSTM1 in sporadic inclusion body myositisSatoshi Nakano, Mitsuaki Oki, Hirofumi KusakaNeuromuscular Disorders : NMD|February 13, 2017
Characterization of pulmonary function in 10-18 year old patients with Duchenne muscular dystrophyThomas Meier, Christian Rummey, Mika Leinonen, et al.Neuromuscular Disorders : NMD|December 14, 2007
Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosisKathrin Huehne, Christiane Zweier, Klaus Raab, et al.Neuromuscular Disorders : NMD|December 14, 2007
X-linked myotubular myopathy and chylothoraxKoenraad SmetsPageof 340