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Neuromuscular Disorders : NMD|January 1, 1995
Congenital symmetrical weakness of the upper limbs resembling brachial plexus palsy: a possible sequel of drug toxicity in first trimester of pregnancy?J Philpot, F Muntoni, S Skellett, et al.Journal of the Neurological Sciences|May 1, 1980
Erythrocyte ghost Na+,K+-adenosine triphosphatase in Duchenne muscular dystrophyM J Dunn, A H Burghes, V DubowitzJournal of Child Neurology|January 1, 1997
Expression of HLA class I antigens in skeletal muscle is a diagnostic marker in juvenile dermatomyositisH Topaloglu, F Muntoni, V Dubowitz, et al.Journal of the Neurological Sciences|October 1, 1983
Rotation-mediated aggregation of skin fibroblasts in Duchenne muscular dystrophy. Effects of monensinJ A Witkowski, H E Statham, V DubowitzNeurology|October 22, 1998
Early onset, autosomal recessive muscular dystrophy with Emery-Dreifuss phenotype and normal emerin expressionJ Taylor, C A Sewry, V Dubowitz, et al.Neuropathology and Applied Neurobiology|November 19, 1997
The abnormal expression of utrophin in Duchenne and Becker muscular dystrophy is age relatedJ Taylor, F Muntoni, V Dubowitz, et al.Brain & Development|January 1, 1980
A new approach to the neurological assessment of the preterm and full-term newborn infantL M Dubowitz, V Dubowitz, P Palmer, et al.American Journal of Human Genetics|January 1, 1995
Transcription of the dystrophin gene in normal tissues and in skeletal muscle of a family with X-linked dilated cardiomyopathyF Muntoni, M A Melis, A Ganau, et al.Annals of Neurology|May 1, 1996
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscleH Lerche, N Mitrovic, V Dubowitz, et al.Developmental Medicine and Child Neurology|December 1, 1982
The development of visual function in normal and neurologically abnormal preterm and fullterm infantsA Morante, L M Dubowitz, M Leven, et al.Pageof 24