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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.Muscle & Nerve|August 1, 1988
Therapeutic trial of isaxonine in Duchenne muscular dystrophyJ Z Heckmatt, S A Hyde, A Gabain, et al.Neuromuscular Disorders : NMD|January 1, 1993
Notechis scutatus venom increases the yield of proliferating muscle cells from biopsies of normal and dystrophic canine muscle--a possible source for myoblast transfer studiesL Dux, B J Cooper, C A Sewry, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1985
Effects of chronic low frequency electrical stimulation on normal human tibialis anterior muscleO M Scott, G Vrbová, S A Hyde, et al.Muscle & Nerve|November 1, 1980
Element analysis of skeletal muscle in Duchenne muscular dystrophy using x-ray fluorescence spectrometryC A Maunder-Sewry, R Gorodetsky, R Yarom, et al.Neuromuscular Disorders : NMD|September 1, 1994
Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophyC A Sewry, K Matsumura, K P Campbell, et al.Brain : a Journal of Neurology|December 1, 1985
Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight childrenJ Z Heckmatt, C A Sewry, D Hodes, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1986
Responses of muscles of patients with Duchenne muscular dystrophy to chronic electrical stimulationO M Scott, G Vrbová, S A Hyde, et al.Archives of Disease in Childhood|May 20, 1999
Feeding problems in merosin deficient congenital muscular dystrophyJ Philpot, A Bagnall, C King, et al.American Journal of Human Genetics|July 1, 1997
Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotypeL Campbell, A Potter, J Ignatius, et al.Pageof 31