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Neuromuscular Disorders : NMD|January 1, 1992
The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathiesT R Helliwell, N T Man, G E Morris, et al.Neuromuscular Disorders : NMD|January 1, 1992
Epidemiology of neuromuscular disorders in the under-20 population in Bologna Province, ItalyL Merlini, S B Stagni, E Marri, et al.Neuromuscular Disorders : NMD|January 1, 1992
A chronic myopathy with coated vesicles and tubular massesS Carpenter, G Karpati, P HollandNeuromuscular Disorders : NMD|January 1, 1992
Parameters of human motor unit twitches obtained by intramuscular microstimulationJ M Elek, A Kossev, R Dengler, et al.Neuromuscular Disorders : NMD|January 1, 1992
Severe periodic febrile myalgia in infancy due to carnitine palmitoyltransferase deficiencyR Schiffmann, E Lahat, A SchechterNeuromuscular Disorders : NMD|January 22, 2004
Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI studyE Mercuri, S Messina, M Kinali, et al.Neuromuscular Disorders : NMD|January 22, 2004
Increased resting energy expenditure in subjects with Emery-Dreifuss muscular dystrophyN Vaisman, S Katzenellenbogen, Y NevoNeuromuscular Disorders : NMD|January 22, 2004
A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysisRobert McFarland, Robert W Taylor, Patrick F Chinnery, et al.Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.Neuromuscular Disorders : NMD|December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)G Meola, V Sansone, D Perani, et al.Pageof 340