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Michio Hirano

Showing results (51-60 of 291) with videos related to

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Current Opinion in Neurology|August 14, 2019
Advances in primary mitochondrial myopathiesIsabella Peixoto de Barcelos, Valentina Emmanuele, Michio Hirano
Gastroenterology|October 1, 2009
Recalcitrant vomiting, disturbed eye movements, and leukoencephalopathy. Mitochondrial neurogastrointestinal encephalomyopathyVincent Zimmer, Anna Zimmer, Michio Hirano, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 15, 2014
Diagnosis of mitochondrial neurogastrointestinal encephalomyopathy: proposal of a clinical algorithmVincent Zimmer, Michio Hirano, Anna Zimmer, et al.
Neuromuscular Disorders : NMD|February 12, 2008
Lack of founder effect for an identical mtDNA depletion syndrome (MDS)-associated MPV17 mutation shared by Navajos and ItaliansAntonella Spinazzola, Valeria Massa, Michio Hirano, et al.
Internal Medicine (Tokyo, Japan)|November 2, 2006
Thymidine phosphorylase gene mutations cause mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Michio Hirano, Ichizo Nishino, Yutaka Nishigaki, et al.
Neuromuscular Disorders : NMD|October 28, 2017
International Workshop:: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adults. Consensus recommendations. 16-18 November 2016, Rome, ItalyMichelangelo Mancuso, Robert McFarland, Thomas Klopstock, et al.
Human Molecular Genetics|October 14, 2010
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensationBeatriz Dorado, Estela Area, Hasan O Akman, et al.
The Journal of Clinical Investigation|June 19, 2003
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiencyYutaka Nishigaki, Ramon Martí, William C Copeland, et al.
Neuromuscular Disorders : NMD|May 31, 2022
232nd ENMC international workshop: Recommendations for treatment of mitochondrial DNA maintenance disorders. 16 - 18 June 2017, Heemskerk, The NetherlandsCarlos López-Gómez, Yolanda Cámara, Michio Hirano, et al.
Biofactors (Oxford, England)|December 30, 2003
Primary coenzyme Q10 deficiency and the brainAli Naini, Vernice-Jackson Lewis, Michio Hirano, et al.
Pageof 30

Showing results (51-60 of 291) with videos related to

Sort By:
Pageof 30
Current Opinion in Neurology|August 14, 2019
Advances in primary mitochondrial myopathiesIsabella Peixoto de Barcelos, Valentina Emmanuele, Michio Hirano
Gastroenterology|October 1, 2009
Recalcitrant vomiting, disturbed eye movements, and leukoencephalopathy. Mitochondrial neurogastrointestinal encephalomyopathyVincent Zimmer, Anna Zimmer, Michio Hirano, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 15, 2014
Diagnosis of mitochondrial neurogastrointestinal encephalomyopathy: proposal of a clinical algorithmVincent Zimmer, Michio Hirano, Anna Zimmer, et al.
Neuromuscular Disorders : NMD|February 12, 2008
Lack of founder effect for an identical mtDNA depletion syndrome (MDS)-associated MPV17 mutation shared by Navajos and ItaliansAntonella Spinazzola, Valeria Massa, Michio Hirano, et al.
Internal Medicine (Tokyo, Japan)|November 2, 2006
Thymidine phosphorylase gene mutations cause mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Michio Hirano, Ichizo Nishino, Yutaka Nishigaki, et al.
Neuromuscular Disorders : NMD|October 28, 2017
International Workshop:: Outcome measures and clinical trial readiness in primary mitochondrial myopathies in children and adults. Consensus recommendations. 16-18 November 2016, Rome, ItalyMichelangelo Mancuso, Robert McFarland, Thomas Klopstock, et al.
Human Molecular Genetics|October 14, 2010
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensationBeatriz Dorado, Estela Area, Hasan O Akman, et al.
The Journal of Clinical Investigation|June 19, 2003
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiencyYutaka Nishigaki, Ramon Martí, William C Copeland, et al.
Neuromuscular Disorders : NMD|May 31, 2022
232nd ENMC international workshop: Recommendations for treatment of mitochondrial DNA maintenance disorders. 16 - 18 June 2017, Heemskerk, The NetherlandsCarlos López-Gómez, Yolanda Cámara, Michio Hirano, et al.
Biofactors (Oxford, England)|December 30, 2003
Primary coenzyme Q10 deficiency and the brainAli Naini, Vernice-Jackson Lewis, Michio Hirano, et al.
Pageof 30