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Neuromuscular Disorders : NMD|December 5, 2008
An unusual complication of immunosuppression in myasthenia gravis: progressive multifocal leukoencephalopathyMuhteşem Gedizlioglu, Pinar Coban, Pinar Ce, et al.Neuromuscular Disorders : NMD|December 6, 2008
Polysaccharide storage myopathy phenotype in quarter horse-related breeds is modified by the presence of an RYR1 mutationM E McCue, S J Valberg, M Jackson, et al.Neuromuscular Disorders : NMD|March 28, 2009
WITHDRAWN: P.P.2 04 Chronological observation of glucose intolerance in myotonic dystrophyH Takada, S Kon, Y OyamaNeuromuscular Disorders : NMD|October 23, 2009
The PedsQL in pediatric patients with Spinal Muscular Atrophy: feasibility, reliability, and validity of the Pediatric Quality of Life Inventory Generic Core Scales and Neuromuscular ModuleSusan T Iannaccone, Linda S Hynan, Anne Morton, et al.Neuromuscular Disorders : NMD|October 27, 2009
Novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia and multisystem failureS Bohlega, G Van Goethem, A Al Semari, et al.Neuromuscular Disorders : NMD|February 13, 2010
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophyGerardo Nigro, Vincenzo Russo, Vega Maria Ventriglia, et al.Neuromuscular Disorders : NMD|December 24, 2005
Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IVNathalie Verpoorten, Kristl G Claeys, Liesbet Deprez, et al.Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.Neuromuscular Disorders : NMD|February 23, 2010
The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathyPeter Reilich, Benedikt Schoser, Nicolai Schramm, et al.Neuromuscular Disorders : NMD|September 11, 2016
Phosphoglycerate mutase deficiency (glycogen storage disease X) caused by a novel variant in PGAM-MBenjamin Koo, Bjorn OskarssonPageof 340