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Neuromuscular Disorders : NMD|January 1, 1994
Experimental regeneration in canine muscular dystrophy--2. Expression of myosin heavy chain isoformsL A Wilson, L Dux, B J Cooper, et al.Archives of Disease in Childhood|June 1, 1984
Diagnostic needle muscle biopsy. A practical and reliable alternative to open biopsyJ Z Heckmatt, A Moosa, C Hutson, et al.Neuromuscular Disorders : NMD|June 19, 2001
Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?J Philpot, S Counsell, G Bydder, et al.Neuromuscular Disorders : NMD|March 1, 1994
Continuous muscle fibre activity (Isaacs' syndrome) in infancy: a report of two casesN H Thomas, J Z Heckmatt, E Rodillo, et al.Journal of Medical Genetics|April 1, 1985
Cell surface abnormality in clones of skin fibroblasts from a carrier of Duchenne muscular dystrophyJ Hillier, G E Jones, H E Statham, et al.American Journal of Human Genetics|November 1, 1993
Exon skipping and translation in patients with frameshift deletions in the dystrophin geneT G Sherratt, T Vulliamy, V Dubowitz, et al.Neuromuscular Disorders : NMD|January 1, 1992
Experimental regeneration in canine muscular dystrophy--1. Immunocytochemical evaluation of dystrophin and beta-spectrin expressionC A Sewry, L A Wilson, L Dux, et al.Clinical and Experimental Rheumatology|July 1, 1994
Juvenile dermatomyositis: serial studies of circulating autoantibodies to a 56kD nuclear proteinG Cambridge, E Ovadia, D A Isenberg, et al.The Histochemical Journal|August 1, 1993
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscleA Clerk, G E Morris, V Dubowitz, et al.Journal of the Neurological Sciences|November 1, 1987
Immunocytochemical localisation of complement components C8 and C9 in human diseased muscle. The role of complement in muscle fibre damageC A Sewry, V Dubowitz, A Abraha, et al.Pageof 31