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Human Genetics|October 30, 1999
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?M D'Alessandro, I Naom, A Ferlini, et al.Journal of the Neurological Sciences|November 1, 1988
Dystrophin and nebulin in the muscular dystrophiesK Patel, T Voit, M J Dunn, et al.Neurology|July 1, 1981
An X-linked disease of the nervous system with disordered copper metabolism and features differing from Menkes diseaseR H Haas, A Robinson, K Evans, et al.The Journal of Pediatrics|July 1, 1981
Neurologic signs in neonatal intraventricular hemorrhage: a correlation with real-time ultrasoundL M Dubowitz, M I Levene, A Morante, et al.Neuromuscular Disorders : NMD|March 1, 1994
Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophyC A Sewry, A Sansome, K Matsumura, et al.Neuromuscular Disorders : NMD|November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritanceA Y Manzur, C A Sewry, J Ziprin, et al.Neuropathology and Applied Neurobiology|August 1, 1994
Expression of utrophin (dystrophin-related protein) during regeneration and maturation of skeletal muscle in canine X-linked muscular dystrophyL A Wilson, B J Cooper, L Dux, et al.Developmental Medicine and Child Neurology|February 1, 1992
The effect of pethidine on the neonatal EEGD G Eaton, D Wertheim, R Oozeer, et al.The Journal of General Virology|June 1, 1990
Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNAL Cunningham, N E Bowles, R J Lane, et al.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.Pageof 24