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American Heart Journal|September 15, 1998
Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophyN Spyrou, J Philpot, R Foale, et al.The European Respiratory Journal|October 12, 2000
Outcome of paediatric domiciliary mask ventilation in neuromuscular and skeletal diseaseA K Simonds, S Ward, S Heather, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary alpha2 laminin deficiency unlinked to the LAMA2 locus on 6q22F Muntoni, J Taylor, C A Sewry, et al.Cellular and Molecular Life Sciences : CMLS|May 4, 2005
Congenital muscular dystrophy: molecular and cellular aspectsC Jimenez-Mallebrera, S C Brown, C A Sewry, et al.Brain Research|November 25, 1985
Low doses of ethanol activate dopaminergic neurons in the ventral tegmental areaG L Gessa, F Muntoni, M Collu, 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.European Journal of Human Genetics : EJHG|April 11, 2000
Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardationH Jin, R J Gardner, R Viswesvaraiah, et al.Pageof 166