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Neuromuscular Disorders : NMD|July 11, 2013
Lactate metabolism during exercise in patients with mitochondrial myopathyTina D Jeppesen, Mette C Orngreen, Gerrit Van Hall, et al.Neuromuscular Disorders : NMD|July 2, 2013
Six minute walk test in type III spinal muscular atrophy: a 12month longitudinal studyE Mazzone, F Bianco, M Main, et al.Neuromuscular Disorders : NMD|July 2, 2013
Muscle MRI reveals distinct abnormalities in genetically proven non-dystrophic myotoniasJasper M Morrow, Emma Matthews, Dipa L Raja Rayan, et al.Neuromuscular Disorders : NMD|January 1, 2013
The Rasch-built Pompe-specific activity (R-PAct) scaleN A M E van der Beek, M L C Hagemans, A T van der Ploeg, et al.Neuromuscular Disorders : NMD|January 12, 2013
A de novo dominant mutation in ACTA1 causing congenital nemaline myopathy associated with a milder phenotype: expanding the spectrum of dominant ACTA1 mutationsL Levesque, M R Del Bigio, S Krawitz, et al.Neuromuscular Disorders : NMD|April 6, 2012
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 geneRune Østern, Toril Fagerheim, Kristin Ørstavik, et al.Neuromuscular Disorders : NMD|February 5, 2013
A novel mutation in the DNM2 gene impairs dynamin 2 localization in skeletal muscle of a patient with late onset centronuclear myopathyBiruta Kierdaszuk, Mariusz Berdynski, Justyna Karolczak, et al.Neuromuscular Disorders : NMD|March 12, 2013
Muscular dystrophy in dysferlin-deficient mouse modelsMark A Hornsey, Steven H Laval, Rita Barresi, et al.Neuromuscular Disorders : NMD|May 8, 2012
Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory responseTatiana V Cohen, Jonathan E Cohen, Terence A PartridgeNeuromuscular Disorders : NMD|March 5, 2013
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Tyler Mark Pierson, Thomas Markello, John Accardi, et al.Pageof 340