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Neuromuscular Disorders : NMD|July 16, 2002
A curious experiment: the paradigm switch from observation and speculation to experimentation, in the understanding of neuromuscular function and diseaseJohn PearnNeuromuscular Disorders : NMD|September 5, 2002
Congenital muscular dystrophy with adducted thumbs, ptosis, external ophthalmoplegia, mental retardation and cerebellar hypoplasia: a novel form of CMDTh Voit, E Parano, V Straub, et al.Neuromuscular Disorders : NMD|September 5, 2002
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 geneR A C van de Wetering, A A W M Gabreëls-Festen, V Timmerman, et al.Neuromuscular Disorders : NMD|September 5, 2002
Nebulin mutations in autosomal recessive nemaline myopathy: an updateKatarina Pelin, Kati Donner, Maria Holmberg, et al.Neuromuscular Disorders : NMD|May 1, 1993
Congenital myasthenic syndromesP Shillito, A Vincent, J Newsom-DavisNeuromuscular Disorders : NMD|May 1, 1993
MELAS point mutation with unusual clinical presentationA L Shanske, S Shanske, G Silvestri, et al.Neuromuscular Disorders : NMD|May 1, 1993
Oral phosphate supplements reverse skeletal muscle abnormalities in a case of chronic fatigue with idiopathic renal hypophosphatemiaJ M Land, G J Kemp, D J Taylor, et al.Neuromuscular Disorders : NMD|May 1, 1995
TTR exon scanning in peripheral neuropathiesM de F Torres, M do R Almeida, M J SaraivaNeuromuscular Disorders : NMD|December 1, 1996
Clinical and genetic study of chronic (types II and III) childhood onset spinal muscular atrophyF Souchon, L R Simard, S Lebrun, et al.Neuromuscular Disorders : NMD|December 1, 1996
Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communitiesM Fardeau, B Eymard, C Mignard, et al.Pageof 341