J S Neerunjun|V Dubowitz - JoVE Visualize

Showing results (181-190 of 240) with videos related to

Pageof 24

Sort By:

Human Genetics|December 1, 1986

A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.

The Journal of Pediatrics|September 1, 1984

Correlation of neurologic assessment in the preterm newborn infant with outcome at 1 yearL M Dubowitz, V Dubowitz, P G Palmer, et al.

Human Genetics|March 1, 1987

DNA deletions in mild and severe Becker muscular dystrophyK A Hart, S Hodgson, A Walker, et al.

Neuromuscular Disorders : NMD|November 26, 1998

Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophyI Naom, M D'Alessandro, C A Sewry, et al.

Journal of Medical Genetics|March 1, 1987

The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophyS Hodgson, A Walker, C Cole, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental abilityS V Hodgson, S Abbs, S Clark, et al.

Neuromuscular Disorders : NMD|June 6, 2000

High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophyD J Dubowitz, J M Tyszka, C A Sewry, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|October 26, 1981

Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activationD W Moss, K B Whitaker, C Parmar, et al.

Biochemical Society Symposium|January 1, 1987

The role of Coxsackie B viruses in the pathogenesis of myocarditis, dilated cardiomyopathy and inflammatory muscle diseaseL C Archard, P J Richardson, E G Olsen, et al.

American Journal of Medical Genetics|August 28, 1995

Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophinLe Thiet Thanh, Nguyen Thi Man, S Hori, et al.

Pageof 24

Showing results (181-190 of 240) with videos related to

Sort By:

Pageof 24

Human Genetics|December 1, 1986

A linkage study of Emery-Dreifuss muscular dystrophyS Hodgson, E Boswinkel, C Cole, et al.

The Journal of Pediatrics|September 1, 1984

Correlation of neurologic assessment in the preterm newborn infant with outcome at 1 yearL M Dubowitz, V Dubowitz, P G Palmer, et al.

Human Genetics|March 1, 1987

DNA deletions in mild and severe Becker muscular dystrophyK A Hart, S Hodgson, A Walker, et al.

Neuromuscular Disorders : NMD|November 26, 1998

Laminin alpha 2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophyI Naom, M D'Alessandro, C A Sewry, et al.

Journal of Medical Genetics|March 1, 1987

The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophyS Hodgson, A Walker, C Cole, et al.

Neuromuscular Disorders : NMD|January 1, 1992

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental abilityS V Hodgson, S Abbs, S Clark, et al.

Neuromuscular Disorders : NMD|June 6, 2000

High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophyD J Dubowitz, J M Tyszka, C A Sewry, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|October 26, 1981

Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activationD W Moss, K B Whitaker, C Parmar, et al.

Biochemical Society Symposium|January 1, 1987

The role of Coxsackie B viruses in the pathogenesis of myocarditis, dilated cardiomyopathy and inflammatory muscle diseaseL C Archard, P J Richardson, E G Olsen, et al.

American Journal of Medical Genetics|August 28, 1995

Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophinLe Thiet Thanh, Nguyen Thi Man, S Hori, et al.

Pageof 24