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Michio Hirano

Showing results (61-70 of 291) with videos related to

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Nature Reviews. Neurology|July 10, 2013
The clinical maze of mitochondrial neurologySalvatore DiMauro, Eric A Schon, Valerio Carelli, et al.
Clinical Chemistry and Laboratory Medicine|August 28, 2003
Alteration of nucleotide metabolism: a new mechanism for mitochondrial disordersRamon Martí, Yutaka Nishigaki, Maya R Vilá, et al.
Plos One|February 24, 2012
Effects of inhibiting CoQ10 biosynthesis with 4-nitrobenzoate in human fibroblastsCatarina M Quinzii, Saba Tadesse, Ali Naini, et al.
Journal of Neuromuscular Diseases|January 31, 2022
Advances in Thymidine Kinase 2 Deficiency: Clinical Aspects, Translational Progress, and Emerging TherapiesAndres Berardo, Cristina Domínguez-González, Kristin Engelstad, et al.
Muscle & Nerve|February 13, 2010
Myopathy and parkinsonism in phosphoglycerate kinase deficiencyEvangelia Sotiriou, Paul Greene, Sindu Krishna, et al.
Trends in Molecular Medicine|June 18, 2010
Therapeutic prospects for mitochondrial diseaseEric A Schon, Salvatore DiMauro, Michio Hirano, et al.
Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.
Advances in Experimental Medicine and Biology|March 13, 2010
Coenzyme Q10 deficiencies in neuromuscular diseasesRafael Artuch, Leonardo Salviati, Sandra Jackson, et al.
Nature Reviews. Genetics|November 3, 2021
Implications of mitochondrial DNA mutations in human induced pluripotent stem cellsValerio Carelli, Michio Hirano, José Antonio Enríquez, et al.
Pharmacotherapy|April 28, 2007
Severe lactic acidosis associated with linezolid use in a patient with the mitochondrial DNA A2706G polymorphismJohn Carson, Jorge Cerda, Jong-Hee Chae, et al.
Pageof 30

Showing results (61-70 of 291) with videos related to

Sort By:
Pageof 30
Nature Reviews. Neurology|July 10, 2013
The clinical maze of mitochondrial neurologySalvatore DiMauro, Eric A Schon, Valerio Carelli, et al.
Clinical Chemistry and Laboratory Medicine|August 28, 2003
Alteration of nucleotide metabolism: a new mechanism for mitochondrial disordersRamon Martí, Yutaka Nishigaki, Maya R Vilá, et al.
Plos One|February 24, 2012
Effects of inhibiting CoQ10 biosynthesis with 4-nitrobenzoate in human fibroblastsCatarina M Quinzii, Saba Tadesse, Ali Naini, et al.
Journal of Neuromuscular Diseases|January 31, 2022
Advances in Thymidine Kinase 2 Deficiency: Clinical Aspects, Translational Progress, and Emerging TherapiesAndres Berardo, Cristina Domínguez-González, Kristin Engelstad, et al.
Muscle & Nerve|February 13, 2010
Myopathy and parkinsonism in phosphoglycerate kinase deficiencyEvangelia Sotiriou, Paul Greene, Sindu Krishna, et al.
Trends in Molecular Medicine|June 18, 2010
Therapeutic prospects for mitochondrial diseaseEric A Schon, Salvatore DiMauro, Michio Hirano, et al.
Neuromuscular Disorders : NMD|February 13, 2010
A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)Andres Berardo, Jorida Coku, Bulent Kurt, et al.
Advances in Experimental Medicine and Biology|March 13, 2010
Coenzyme Q10 deficiencies in neuromuscular diseasesRafael Artuch, Leonardo Salviati, Sandra Jackson, et al.
Nature Reviews. Genetics|November 3, 2021
Implications of mitochondrial DNA mutations in human induced pluripotent stem cellsValerio Carelli, Michio Hirano, José Antonio Enríquez, et al.
Pharmacotherapy|April 28, 2007
Severe lactic acidosis associated with linezolid use in a patient with the mitochondrial DNA A2706G polymorphismJohn Carson, Jorge Cerda, Jong-Hee Chae, et al.
Pageof 30