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V Dubowitz

Showing results (161-170 of 349) with videos related to

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Neuromuscular 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
Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5qV Dubowitz, R J Daniels, K E Davies
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 Dubowitz
Journal 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 Dubowitz
Journal of Medical Genetics|June 1, 1971
Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated casesV Dubowitz, P Cooke, D Colver, et al.
Journal of the Neurological Sciences|July 1, 1971
Morphological studies on normal and diseased human muscle in cultureA Bishop, B Gallup, Y Skeate, 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.
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.
Pageof 35

Showing results (161-170 of 349) with videos related to

Sort By:
Pageof 35
Neuromuscular 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
Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5qV Dubowitz, R J Daniels, K E Davies
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 Dubowitz
Journal 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 Dubowitz
Journal of Medical Genetics|June 1, 1971
Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated casesV Dubowitz, P Cooke, D Colver, et al.
Journal of the Neurological Sciences|July 1, 1971
Morphological studies on normal and diseased human muscle in cultureA Bishop, B Gallup, Y Skeate, 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.
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.
Pageof 35