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Neuromuscular Disorders : NMD|July 16, 2002
An expanding view for the molecular basis of familial periodic paralysisStephen C CannonNeuromuscular Disorders : NMD|July 16, 2002
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian populationM Gross, E Rötzer, P Kölle, et al.Neuromuscular Disorders : NMD|September 1, 1995
Isometric strength and thickness relationships in human quadriceps muscleR J Freilich, R L Kirsner, E ByrneNeuromuscular Disorders : NMD|September 1, 1993
Human skeletal muscle has a voltage-gated proton currentR M Krause, L Bernheim, C R BaderNeuromuscular Disorders : NMD|March 1, 1993
Deficiency of dystrophin-associated proteins: a common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophiesK Matsumura, K P CampbellNeuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.Neuromuscular Disorders : NMD|July 1, 1995
Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both lociS Tsujino, S Shanske, J E Carroll, et al.Neuromuscular Disorders : NMD|July 1, 1995
Expression of laminin subunits in congenital muscular dystrophyC A Sewry, J Philpot, D Mahony, et al.Neuromuscular Disorders : NMD|May 1, 1995
Phospholipase A2 activity in dystrophinopathiesM Lindahl, E Bäckman, K G Henriksson, et al.Neuromuscular Disorders : NMD|May 1, 1995
Low-dose prednisolone treatment in Duchenne and Becker muscular dystrophyE Bäckman, K G HenrikssonPageof 340