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S Dimauro

Showing results (41-50 of 421) with videos related to

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Advances in Pediatrics|January 1, 1994
Hereditary metabolic cardiomyopathiesS Servidei, E Bertini, S DiMauro
Biology of the Neonate|January 1, 1990
Mitochondrial defects of brain and muscleD C De Vivo, S DiMauro
Annals of Neurology|July 1, 1996
Genetic heterogeneity in Leigh syndromeS DiMauro, D C De Vivo
The Journal of Pediatrics|September 1, 1994
Myophosphorylase deficiency: an unusually severe form with myoglobinuriaK Kristjánsson, S Tsujino, S DiMauro
Revue Neurologique|January 1, 1989
Mitochondrial encephalomyopathiesA Lombes, E Bonilla, S Dimauro
Neurologic Clinics|February 5, 2000
Glycogen storage myopathiesS Tsujino, I Nonaka, S DiMauro
The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauro
Current Opinion in Cardiology|May 18, 2001
Mitochondria and the heartM Hirano, M Davidson, S DiMauro
Journal of Neuropathology and Experimental Neurology|July 1, 1971
Nervous system in Pompe's disease. Ultrastructure and biochemistryP Gambetti, S DiMauro, L Baker
Experimental Neurology|June 1, 1984
Multiple neutral maltase activities in normal and acid maltase-deficient human muscleS Shanske, N Bresolin, S DiMauro
Pageof 43

Showing results (41-50 of 421) with videos related to

Sort By:
Pageof 43
Advances in Pediatrics|January 1, 1994
Hereditary metabolic cardiomyopathiesS Servidei, E Bertini, S DiMauro
Biology of the Neonate|January 1, 1990
Mitochondrial defects of brain and muscleD C De Vivo, S DiMauro
Annals of Neurology|July 1, 1996
Genetic heterogeneity in Leigh syndromeS DiMauro, D C De Vivo
The Journal of Pediatrics|September 1, 1994
Myophosphorylase deficiency: an unusually severe form with myoglobinuriaK Kristjánsson, S Tsujino, S DiMauro
Revue Neurologique|January 1, 1989
Mitochondrial encephalomyopathiesA Lombes, E Bonilla, S Dimauro
Neurologic Clinics|February 5, 2000
Glycogen storage myopathiesS Tsujino, I Nonaka, S DiMauro
The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauro
Current Opinion in Cardiology|May 18, 2001
Mitochondria and the heartM Hirano, M Davidson, S DiMauro
Journal of Neuropathology and Experimental Neurology|July 1, 1971
Nervous system in Pompe's disease. Ultrastructure and biochemistryP Gambetti, S DiMauro, L Baker
Experimental Neurology|June 1, 1984
Multiple neutral maltase activities in normal and acid maltase-deficient human muscleS Shanske, N Bresolin, S DiMauro
Pageof 43