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DiMauro

Showing results (151-160 of 1,071) with videos related to

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Transactions of the American Neurological Association|January 1, 1981
Phosphoglycerate kinase deficiency: a new cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Muscle & Nerve|July 1, 2006
Approaches to the treatment of mitochondrial diseasesSalvatore DiMauro, Michio Hirano, Eric A Schon
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1988
[Cardiac rhythm in the newborn infant. A contribution to the definition of normality]P E Dimauro, M Pandolfi, I Giani
Nature Reviews. Genetics|November 17, 2012
Human mitochondrial DNA: roles of inherited and somatic mutationsEric A Schon, Salvatore DiMauro, Michio Hirano
The New England Journal of Medicine|July 3, 2014
Mutant COQ2 in multiple-system atrophyCatarina M Quinzii, Michio Hirano, Salvatore DiMauro
Redox Biology|March 5, 2020
Exercise, redox homeostasis and the epigenetic landscapeIvan Dimauro, Maria Paola Paronetto, Daniela Caporossi
Advances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivo
Revista De Neurologia|April 2, 1999
[Mitochondrial encephalopathies: where are we going?]S DiMauro, A L Andreu, E Bonilla
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
Pageof 108

Showing results (151-160 of 1,071) with videos related to

Sort By:
Pageof 108
Transactions of the American Neurological Association|January 1, 1981
Phosphoglycerate kinase deficiency: a new cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Muscle & Nerve|July 1, 2006
Approaches to the treatment of mitochondrial diseasesSalvatore DiMauro, Michio Hirano, Eric A Schon
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1988
[Cardiac rhythm in the newborn infant. A contribution to the definition of normality]P E Dimauro, M Pandolfi, I Giani
Nature Reviews. Genetics|November 17, 2012
Human mitochondrial DNA: roles of inherited and somatic mutationsEric A Schon, Salvatore DiMauro, Michio Hirano
The New England Journal of Medicine|July 3, 2014
Mutant COQ2 in multiple-system atrophyCatarina M Quinzii, Michio Hirano, Salvatore DiMauro
Redox Biology|March 5, 2020
Exercise, redox homeostasis and the epigenetic landscapeIvan Dimauro, Maria Paola Paronetto, Daniela Caporossi
Advances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivo
Revista De Neurologia|April 2, 1999
[Mitochondrial encephalopathies: where are we going?]S DiMauro, A L Andreu, E Bonilla
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
Pageof 108