A D Roses|P M Conneally - JoVE Visualize

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American Journal of Medical Genetics|January 1, 1988

Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28M Kambouris, S R Dlouhy, J A Trofatter, et al.

Neurology|August 1, 1981

Identification of abnormally [32P]-phosphorylated cyanogen bromide cleavage product of erythrocyte membrane spectrin in Duchenne muscular dystrophyA D Roses, P E Shile, M H Herbstreith, et al.

Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1978

Biochemical relationships between muscle and erythrocyte membrane. Interpretations with respect to Duchenne muscular dystrophyA D Roses, M H Herbstreith, B S Metcalf, et al.

Neurology|May 1, 1977

Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophyA D Roses, M J Roses, G A Nicholson, et al.

Neurology|January 1, 1977

Evaluation and detection of Duchenne's and Becker's muscular dystrophy carriers by manual muscle testingM S Roses, M T Nicholson, C S Kircher, et al.

Science (New York, N.Y.)|November 20, 1973

Phosphorylation of muscle membranes: identification of a membrane-bound protein kinaseC G Andrew, A D Roses, R R Almon, et al.

Neurology|June 1, 1993

Novel polymorphism in the A4 region of the amyloid precursor protein gene in a patient without Alzheimer's diseaseM L Peacock, J T Warren, A D Roses, et al.

The European Journal of Neuroscience|December 21, 2000

Increased neuronal damage and apoE immunoreactivity in human apolipoprotein E, E4 isoform-specific, transgenic mice after global cerebral ischaemiaK Horsburgh, J McCulloch, M Nilsen, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1995

Risk of intracranial aneurysms in families with subarachnoid hemorrhageM J Alberts, A Quinones, C Graffagnino, et al.

Neurology|February 1, 1981

No direct correlation between serum antiacetylcholine receptor antibody levels and clinical state of individual patients with myasthenia gravisA D Roses, C W Olanow, M W McAdams, et al.

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Showing results (111-120 of 362) with videos related to

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Pageof 37

American Journal of Medical Genetics|January 1, 1988

Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28M Kambouris, S R Dlouhy, J A Trofatter, et al.

Neurology|August 1, 1981

Identification of abnormally [32P]-phosphorylated cyanogen bromide cleavage product of erythrocyte membrane spectrin in Duchenne muscular dystrophyA D Roses, P E Shile, M H Herbstreith, et al.

Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1978

Biochemical relationships between muscle and erythrocyte membrane. Interpretations with respect to Duchenne muscular dystrophyA D Roses, M H Herbstreith, B S Metcalf, et al.

Neurology|May 1, 1977

Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophyA D Roses, M J Roses, G A Nicholson, et al.

Neurology|January 1, 1977

Evaluation and detection of Duchenne's and Becker's muscular dystrophy carriers by manual muscle testingM S Roses, M T Nicholson, C S Kircher, et al.

Science (New York, N.Y.)|November 20, 1973

Phosphorylation of muscle membranes: identification of a membrane-bound protein kinaseC G Andrew, A D Roses, R R Almon, et al.

Neurology|June 1, 1993

Novel polymorphism in the A4 region of the amyloid precursor protein gene in a patient without Alzheimer's diseaseM L Peacock, J T Warren, A D Roses, et al.

The European Journal of Neuroscience|December 21, 2000

Increased neuronal damage and apoE immunoreactivity in human apolipoprotein E, E4 isoform-specific, transgenic mice after global cerebral ischaemiaK Horsburgh, J McCulloch, M Nilsen, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1995

Risk of intracranial aneurysms in families with subarachnoid hemorrhageM J Alberts, A Quinones, C Graffagnino, et al.

Neurology|February 1, 1981

No direct correlation between serum antiacetylcholine receptor antibody levels and clinical state of individual patients with myasthenia gravisA D Roses, C W Olanow, M W McAdams, et al.

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