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Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.Neuromuscular Disorders : NMD|January 4, 2011
Reversible demyelinating neuropathy associated with renal cell carcinomaJeffrey A Allen, Ximing J Yang, Robert L SufitNeuromuscular Disorders : NMD|October 22, 2010
Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotypeUluc Yis, Gökhan Uyanik, Pinar Bambul Heck, et al.Neuromuscular Disorders : NMD|October 22, 2010
Prevalence, mutation spectrum and phenotypic variability in Norwegian patients with Limb Girdle Muscular Dystrophy 2IEva Stensland, Sigurd Lindal, Christoffer Jonsrud, et al.Neuromuscular Disorders : NMD|December 8, 2010
Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4Berivan Baskin, William T Gibson, Peter N RayNeuromuscular Disorders : NMD|November 9, 2010
Stem cells to treat muscular dystrophies - where are we?Jinhong Meng, Francesco Muntoni, Jennifer E MorganNeuromuscular Disorders : NMD|March 8, 2011
Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?Robin B FitzsimonsNeuromuscular Disorders : NMD|July 20, 2010
Validation of an automated computational method for skeletal muscle fibre morphometry analysisFleur Garton, Jane T Seto, Kathryn N North, et al.Neuromuscular Disorders : NMD|August 17, 2010
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutationGiorgio Tasca, Massimiliano Mirabella, Aldobrando Broccolini, et al.Neuromuscular Disorders : NMD|May 18, 2010
The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotypeCharlotte L Alston, Andreas Bender, Iain P Hargreaves, et al.Pageof 340