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Neuromuscular Disorders : NMD|October 27, 2009
Prevalence and psychosocial impact of lower urinary tract symptoms in patients with Duchenne muscular dystrophyEvaline van Wijk, Bert J Messelink, Lily Heijnen, et al.Neuromuscular Disorders : NMD|October 27, 2009
Immunolabelling and flow cytometry as new tools to explore dysferlinopathiesN Wein, M Krahn, S Courrier, et al.Neuromuscular Disorders : NMD|June 1, 1997
Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin beta 1?J Taylor, F Muntoni, S Robb, et al.Neuromuscular Disorders : NMD|June 1, 1997
Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channelP Lapie, P Lory, B FontaineNeuromuscular Disorders : NMD|June 1, 1997
From mutation to myotonia in sodium channel disordersS C CannonNeuromuscular Disorders : NMD|June 1, 1997
Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous systemL J PtácekNeuromuscular Disorders : NMD|March 1, 1995
Malignant hyperthermia susceptibility without central core disease (CCD) in a family where CCD is diagnosedG Islander, K G Henriksson, E Ranklev-TwetmanNeuromuscular Disorders : NMD|March 1, 1995
Sarcolemmal expression of dystrophin C-terminus but reduced expression of 6q-dystrophin-related protein in two DMD patients with large deletions of the dystrophin geneR E Bittner, S Shorny, R Ferlings, et al.Neuromuscular Disorders : NMD|September 1, 1993
Behaviour of human atrial myocytes in culture is donor age dependentC Rücker-Martin, S Hatem, I Dubus, et al.Neuromuscular Disorders : NMD|September 1, 1993
Synaptophysin (p38) immunolabelling at the mouse neuromuscular junctionC Colasante, M O Brouard, M Pécot-DechavassinePageof 340