L V Nicholson - JoVE Visualize

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Journal of the Neurological Sciences|December 1, 1989

Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophyL V Nicholson, K Davison, M A Johnson, et al.

Journal of Medical Genetics|August 1, 1992

Investigation of a female manifesting Becker muscular dystrophyI A Glass, L V Nicholson, E Watkiss, et al.

The Journal of Clinical Investigation|February 1, 1992

Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?D Récan, P Chafey, F Leturcq, et al.

Human Genetics|December 1, 1991

Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophyK M Bushby, N J Cleghorn, A Curtis, et al.

Journal of Neurology|February 1, 1993

The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalitiesK M Bushby, D Gardner-Medwin, L V Nicholson, et al.

FEBS Letters|April 22, 1991

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice. Immunological evidenceF Pons, N Augier, J O Léger, et al.

Neuromuscular Disorders : NMD|May 1, 1995

Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriersP M Matthews, D Benjamin, I Van Bakel, et al.

Nature|January 11, 1990

Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.

Journal of Medical Genetics|September 1, 1993

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groupsL V Nicholson, M A Johnson, K M Bushby, et al.

Journal of Medical Genetics|September 1, 1993

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patientsL V Nicholson, M A Johnson, K M Bushby, et al.

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Showing results (31-40 of 41) with videos related to

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Pageof 5

Journal of the Neurological Sciences|December 1, 1989

Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophyL V Nicholson, K Davison, M A Johnson, et al.

Journal of Medical Genetics|August 1, 1992

Investigation of a female manifesting Becker muscular dystrophyI A Glass, L V Nicholson, E Watkiss, et al.

The Journal of Clinical Investigation|February 1, 1992

Are cysteine-rich and COOH-terminal domains of dystrophin critical for sarcolemmal localization?D Récan, P Chafey, F Leturcq, et al.

Human Genetics|December 1, 1991

Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophyK M Bushby, N J Cleghorn, A Curtis, et al.

Journal of Neurology|February 1, 1993

The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalitiesK M Bushby, D Gardner-Medwin, L V Nicholson, et al.

FEBS Letters|April 22, 1991

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice. Immunological evidenceF Pons, N Augier, J O Léger, et al.

Neuromuscular Disorders : NMD|May 1, 1995

Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriersP M Matthews, D Benjamin, I Van Bakel, et al.

Nature|January 11, 1990

Very mild muscular dystrophy associated with the deletion of 46% of dystrophinS B England, L V Nicholson, M A Johnson, et al.

Journal of Medical Genetics|September 1, 1993

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groupsL V Nicholson, M A Johnson, K M Bushby, et al.

Journal of Medical Genetics|September 1, 1993

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patientsL V Nicholson, M A Johnson, K M Bushby, et al.

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