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Neuromuscular Disorders : NMD|July 19, 2000
Childhood chronic inflammatory demyelinating polyneuropathy: clinical course and long-term outcomeM M Ryan, P J Grattan-Smith, P G Procopis, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Diffusion of information about genetic risk within familiesSégolène Ayme, Geneviève Macquart-Moulin, Claire Julian-Reynier, et al.
Neuromuscular Disorders : NMD|December 4, 2001
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantationF M Santorelli, M G Gagliardi, C Dionisi-Vici, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Non-toxic ubiquitous over-expression of utrophin in the mdx mouseR Fisher, J M Tinsley, S R Phelps, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblastsD Furling, D Lemieux, K Taneja, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Muscle development genes: their relevance in neuromuscular disordersFrancesco Muntoni, Sue Brown, Caroline Sewry, et al.
Neuromuscular Disorders : NMD|May 29, 2002
Ageing muscle: clonal expansions of mitochondrial DNA point mutations and deletions cause focal impairment of mitochondrial functionGuillemette Fayet, Monica Jansson, Damien Sternberg, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Spinal muscular atrophy among the Roma (Gypsies) in Bulgaria and HungaryAlbena Jordanova, Veronika Kargaci, Ivo Kremensky, et al.
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