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Neuromuscular Disorders : NMD|July 16, 2002
Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?M M O Tonini, M R Passos-Bueno, A Cerqueira, et al.
Neuropediatrics|May 1, 1987
Neurological, electrophysiological and MRI abnormalities in infants with extensive cystic leukomalaciaL S De Vries, J A Connell, L M Dubowitz, et al.
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.
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.
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.
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