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DiMauro

Showing results (141-150 of 1,071) with videos related to

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Pediatric Nursing|February 7, 2018
Pediatric Diabetes Telemedicine Program Improves Access to Care for Rural Families: Role of APRNsNancy Marie Smith, Rosemarie DiMauro Satyshur
Muscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauro
Neurologic Clinics|November 16, 2002
Mitochondrial diseasesTuan H Vu, Michio Hirano, Salvatore DiMauro
Molecular and Cellular Biochemistry|October 6, 1997
Carnitine palmitoyltransferase II deficiency: diagnosis by molecular analysis of bloodP Kaufmann, M el-Schahawi, S DiMauro
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
Journal of Bioenergetics and Biomembranes|April 1, 1997
Mitochondrial DNA mutations and pathogenesisE A Schon, E Bonilla, S DiMauro
Neurochemical Research|November 10, 2006
Human coenzyme Q10 deficiencyCatarina M Quinzii, Salvatore DiMauro, Michio Hirano
The Journal of Clinical Investigation|March 3, 2007
Mutations in coenzyme Q10 biosynthetic genesSalvatore DiMauro, Catarina M Quinzii, Michio Hirano
Annals of Neurology|January 1, 1983
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Advances in Experimental Medicine and Biology|June 26, 2012
The many clinical faces of cytochrome c oxidase deficiencySalvatore DiMauro, Kurenai Tanji, Eric A Schon
Pageof 108

Showing results (141-150 of 1,071) with videos related to

Sort By:
Pageof 108
Pediatric Nursing|February 7, 2018
Pediatric Diabetes Telemedicine Program Improves Access to Care for Rural Families: Role of APRNsNancy Marie Smith, Rosemarie DiMauro Satyshur
Muscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauro
Neurologic Clinics|November 16, 2002
Mitochondrial diseasesTuan H Vu, Michio Hirano, Salvatore DiMauro
Molecular and Cellular Biochemistry|October 6, 1997
Carnitine palmitoyltransferase II deficiency: diagnosis by molecular analysis of bloodP Kaufmann, M el-Schahawi, S DiMauro
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
Journal of Bioenergetics and Biomembranes|April 1, 1997
Mitochondrial DNA mutations and pathogenesisE A Schon, E Bonilla, S DiMauro
Neurochemical Research|November 10, 2006
Human coenzyme Q10 deficiencyCatarina M Quinzii, Salvatore DiMauro, Michio Hirano
The Journal of Clinical Investigation|March 3, 2007
Mutations in coenzyme Q10 biosynthetic genesSalvatore DiMauro, Catarina M Quinzii, Michio Hirano
Annals of Neurology|January 1, 1983
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Advances in Experimental Medicine and Biology|June 26, 2012
The many clinical faces of cytochrome c oxidase deficiencySalvatore DiMauro, Kurenai Tanji, Eric A Schon
Pageof 108