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V Dubowitz

Showing results (301-310 of 349) with videos related to

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Biochemical Society Transactions|May 1, 1996
The protein defect in congenital muscular dystrophyC A Sewry, I Naom, M D'Alessandro, et al.
Brain : a Journal of Neurology|December 28, 1999
Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophyI Naom, M D'alessandro, C A Sewry, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscleS T Appleyard, M J Dunn, V Dubowitz, et al.
Lancet (London, England)|January 14, 1978
Prenatal diagnosis in Duchenne muscular dystrophy: Salvage of normal male fetusV Dubowitz, B van Iddekinge, C H Rodeck, et al.
Journal of Medical Genetics|February 1, 1996
Gene deletions in spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiencyE Tan, H Topaloglu, C Sewry, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chainC A Sewry, I Naom, M D'Alessandro, et al.
Journal of Medical Genetics|December 1, 1986
The screening of Duchenne muscular dystrophy patients for submicroscopic deletionsK Hart, C Cole, A Walker, et al.
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.
Pageof 35

Showing results (301-310 of 349) with videos related to

Sort By:
Pageof 35
Biochemical Society Transactions|May 1, 1996
The protein defect in congenital muscular dystrophyC A Sewry, I Naom, M D'Alessandro, et al.
Brain : a Journal of Neurology|December 28, 1999
Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophyI Naom, M D'alessandro, C A Sewry, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscleS T Appleyard, M J Dunn, V Dubowitz, et al.
Lancet (London, England)|January 14, 1978
Prenatal diagnosis in Duchenne muscular dystrophy: Salvage of normal male fetusV Dubowitz, B van Iddekinge, C H Rodeck, et al.
Journal of Medical Genetics|February 1, 1996
Gene deletions in spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.
Neuromuscular Disorders : NMD|March 1, 1997
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiencyE Tan, H Topaloglu, C Sewry, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chainC A Sewry, I Naom, M D'Alessandro, et al.
Journal of Medical Genetics|December 1, 1986
The screening of Duchenne muscular dystrophy patients for submicroscopic deletionsK Hart, C Cole, A Walker, et al.
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.
Pageof 35