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S Dimauro

Showing results (61-70 of 421) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Mitochondrial encephalomyopathies: therapeutic approachesS DiMauro, M Hirano, E A Schon
Neurology|July 1, 1978
Active transport of carnitine into skeletal muscleJ H Willner, S Ginsburg, S Dimauro
Advances in Experimental Medicine and Biology|January 1, 1985
Hereditary metabolic myopathiesA F Miranda, T Mongini, S DiMauro
CRC Critical Reviews in Clinical Neurobiology|January 1, 1984
Disorders of glycogen metabolism of muscleS DiMauro, N Bresolin, A P Hays
Journal of Bioenergetics and Biomembranes|June 1, 1994
Mitochondrial encephalomyopathies: clinical and molecular analysisE A Schon, M Hirano, S DiMauro
Muscle & Nerve. Supplement|January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, I Nonaka, et al.
Birth Defects Original Article Series|February 1, 1971
Glycogen storage diseases of muscle problems in biochemical geneticsL P Rowland, S Dimauro, W J Bank
Pediatric Research|September 1, 1973
Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and VS DiMauro, L P Rowland, W J Mellman
Archives of Neurology|December 1, 1979
Adult polysaccharidosis. Clinicopathological, ultrastructural, and biochemical featuresN S Peress, S DiMauro, V A Roxburgh
Archives of Neurology|December 1, 1970
Control of glycogen metabolism in human muscle. Evidence from glycogen storage diseasesS DiMauro, L P Rowland, P M DiMauro
Pageof 43

Showing results (61-70 of 421) with videos related to

Sort By:
Pageof 43
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Mitochondrial encephalomyopathies: therapeutic approachesS DiMauro, M Hirano, E A Schon
Neurology|July 1, 1978
Active transport of carnitine into skeletal muscleJ H Willner, S Ginsburg, S Dimauro
Advances in Experimental Medicine and Biology|January 1, 1985
Hereditary metabolic myopathiesA F Miranda, T Mongini, S DiMauro
CRC Critical Reviews in Clinical Neurobiology|January 1, 1984
Disorders of glycogen metabolism of muscleS DiMauro, N Bresolin, A P Hays
Journal of Bioenergetics and Biomembranes|June 1, 1994
Mitochondrial encephalomyopathies: clinical and molecular analysisE A Schon, M Hirano, S DiMauro
Muscle & Nerve. Supplement|January 1, 1995
The molecular genetic basis of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, I Nonaka, et al.
Birth Defects Original Article Series|February 1, 1971
Glycogen storage diseases of muscle problems in biochemical geneticsL P Rowland, S Dimauro, W J Bank
Pediatric Research|September 1, 1973
Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and VS DiMauro, L P Rowland, W J Mellman
Archives of Neurology|December 1, 1979
Adult polysaccharidosis. Clinicopathological, ultrastructural, and biochemical featuresN S Peress, S DiMauro, V A Roxburgh
Archives of Neurology|December 1, 1970
Control of glycogen metabolism in human muscle. Evidence from glycogen storage diseasesS DiMauro, L P Rowland, P M DiMauro
Pageof 43