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Neuropediatrics|December 22, 1999
Clinical spectrum and diagnostic difficulties of infantile ponto-cerebellar hypoplasia type 1F Muntoni, F Goodwin, C Sewry, et al.
British Medical Journal (Clinical Research Ed.)|September 18, 1982
Nuclear magnetic resonance imaging of the brain in childrenM I Levene, A Whitelaw, V Dubowitz, et al.
Clinical Science (London, England : 1979)|August 1, 1991
Renal haemodynamics of cyclosporin A nephrotoxicity in children with juvenile dermatomyositisA M Peters, J Z Heckmatt, N Hasson, et al.
Neuromuscular Disorders : NMD|April 12, 2001
Early white matter changes on brain magnetic resonance imaging in a newborn affected by merosin-deficient congenital muscular dystrophyE Mercuri, M Rutherford, C De Vile, et al.
The Journal of Clinical Investigation|August 1, 1995
A mutation in the dystrophin gene selectively affecting dystrophin expression in the heartF Muntoni, L Wilson, G Marrosu, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophyC A Sewry, J Taylor, L V Anderson, et al.
Neuropediatrics|June 1, 1995
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changesE Mercuri, L Dubowitz, A Berardinelli, et al.
Lancet (London, England)|July 20, 1985
Predictive value of cranial ultrasound in the newborn baby: a reappraisalL S de Vries, L M Dubowitz, V Dubowitz, et al.
Neuropediatrics|April 4, 2002
Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophyE Mercuri, S Counsell, J Allsop, et al.
Lancet (London, England)|May 13, 1989
Cyclosporin in juvenile dermatomyositisJ Heckmatt, N Hasson, C Saunders, et al.
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