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Clinical and Experimental Rheumatology|January 1, 1989
A comparative study of in vitro proliferative responses to mitogens and immunoglobulin production in patients with inflammatory muscle diseaseG Cambridge, A Faith, C Saunders, et al.Journal of the Neurological Sciences|July 1, 1985
Lobulated fibers in neuromuscular diseasesM J Guerard, C A Sewry, V DubowitzNeuromuscular Disorders : NMD|July 1, 1995
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscleJ Philpot, C Sewry, J Pennock, et al.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 DubowitzLancet (London, England)|July 11, 1992
Low cerebrospinal fluid concentration of free gamma-aminobutyric acid in startle diseaseL M Dubowitz, H Bouza, M F Hird, et al.Neuropediatrics|April 1, 1994
Prediction of outcome in children with congenital hemiplegia: a magnetic resonance imaging studyH Bouza, L M Dubowitz, M Rutherford, et al.Neurology|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.Pageof 31