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Neuromuscular Disorders : NMD|July 1, 1995
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscleJ Philpot, C Sewry, J Pennock, et al.Journal of Child Neurology|January 1, 1997
Expression of HLA class I antigens in skeletal muscle is a diagnostic marker in juvenile dermatomyositisH Topaloglu, F Muntoni, V Dubowitz, et al.Journal of Child Neurology|November 1, 1995
Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophyZ Shorer, J Philpot, F Muntoni, et al.Annals of the Rheumatic Diseases|March 1, 1991
Rhabdomyolysis after intramuscular iron-dextran in malabsorptionW D Foulkes, C Sewry, J Calam, 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.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 19, 2000
Diaphragmatic spinal muscular atrophy with bulbar weaknessE Mercuri, F Goodwin, C Sewry, et al.Neuromuscular Disorders : NMD|January 5, 2000
Expression, regulation and localisation of dystrophin isoforms in human foetal skeletal and cardiac muscleS Torelli, A Ferlini, L Obici, et al.Neuromuscular Disorders : NMD|July 17, 1999
X-linked dilated cardiomyopathy and the dystrophin geneA Ferlini, C Sewry, M A Melis, et al.Pediatric Neurology|July 3, 1998
Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophyE Mercuri, S Anker, J Philpot, et al.Pageof 7