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Neuromuscular Disorders : NMD|December 6, 2017
A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophyNathalie Goemans, Eugenio Mercuri, Elena Belousova, et al.Neuromuscular Disorders : NMD|June 2, 2012
The multifaceted character of lymphotoxin β in inflammatory myopathies and muscular dystrophiesKim K Creus, Boel De Paepe, Joachim Weis, et al.Neuromuscular Disorders : NMD|April 18, 2012
MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscleEmma L Blakely, Anna Butterworth, Robert D M Hadden, et al.Neuromuscular Disorders : NMD|August 11, 2015
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1Giorgio Tasca, Adele D'Amico, Mauro Monforte, et al.Neuromuscular Disorders : NMD|August 1, 2015
Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot-Marie-Tooth diseaseKathryn M Brennan, Yunhong Bai, Chiara Pisciotta, et al.Neuromuscular Disorders : NMD|December 18, 2013
Early infantile sensory-motor neuropathy with late onset respiratory distressAstrid Blaschek, Dieter Gläser, Marius Kuhn, et al.Neuromuscular Disorders : NMD|May 31, 2017
Novel truncating variant in DNA2-related congenital onset myopathy and ptosis suggests genotype-phenotype correlationP Phowthongkum, A SunNeuromuscular Disorders : NMD|May 12, 2018
Diaphragmatic dysfunction as the presenting symptom in neuromuscular disorders: A retrospective longitudinal study of etiology and outcome in 30 German patientsMatthias Türk, Irina Weber, Gernot Vogt-Ladner, et al.Neuromuscular Disorders : NMD|June 19, 2017
Insights from genotype-phenotype correlations by novel SPEG mutations causing centronuclear myopathyHaicui Wang, Claudia Castiglioni, Ayşe Kaçar Bayram, et al.Neuromuscular Disorders : NMD|June 19, 2017
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domainsElizabeth Harris, Umar Burki, Chiara Marini-Bettolo, et al.Pageof 341