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Claude Jardel

Showing results (31-40 of 52) with videos related to

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Frontiers in Neurology|October 23, 2019
Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic VariantsAriadna González-Del Angel, Michela Bisciglia, Steven Vargas-Cañas, et al.
Mitochondrion|April 3, 2014
Phenotypic diversity associated with the MT-TV gene m.1644G>A mutation, a matter of quantityMatthew J Fraidakis, Claude Jardel, Stéphane Allouche, et al.
AIDS (London, England)|May 7, 2009
Long-term follow-up of liver transplanted HIV/hepatitis B virus coinfected patients: perfect control of hepatitis B virus replication and absence of mitochondrial toxicityMariagrazia Tateo, Anne-Marie Roque-Afonso, Teresa Maria Antonini, et al.
Molecular Genetics and Metabolism|March 20, 2013
Exercise intolerance in Glycogen Storage Disease Type III: weakness or energy deficiency?Nicolai Preisler, Agnès Pradel, Edith Husu, et al.
Journal of Inherited Metabolic Disease|February 10, 2018
Targeted versus untargeted omics - the CAFSA storyMaria Del Mar Amador, Benoit Colsch, Foudil Lamari, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 6, 2018
eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing dataDavid Goudenège, Celine Bris, Virginie Hoffmann, et al.
Journal of Hepatology|May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fastingLaura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Impaired glucose tolerance in patients with amyotrophic lateral sclerosisPierre-Francois Pradat, Gaelle Bruneteau, Paul H Gordon, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
Plos Genetics|March 28, 2015
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesisAymeric Chartier, Pierre Klein, Stéphanie Pierson, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Frontiers in Neurology|October 23, 2019
Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic VariantsAriadna González-Del Angel, Michela Bisciglia, Steven Vargas-Cañas, et al.
Mitochondrion|April 3, 2014
Phenotypic diversity associated with the MT-TV gene m.1644G>A mutation, a matter of quantityMatthew J Fraidakis, Claude Jardel, Stéphane Allouche, et al.
AIDS (London, England)|May 7, 2009
Long-term follow-up of liver transplanted HIV/hepatitis B virus coinfected patients: perfect control of hepatitis B virus replication and absence of mitochondrial toxicityMariagrazia Tateo, Anne-Marie Roque-Afonso, Teresa Maria Antonini, et al.
Molecular Genetics and Metabolism|March 20, 2013
Exercise intolerance in Glycogen Storage Disease Type III: weakness or energy deficiency?Nicolai Preisler, Agnès Pradel, Edith Husu, et al.
Journal of Inherited Metabolic Disease|February 10, 2018
Targeted versus untargeted omics - the CAFSA storyMaria Del Mar Amador, Benoit Colsch, Foudil Lamari, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 6, 2018
eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing dataDavid Goudenège, Celine Bris, Virginie Hoffmann, et al.
Journal of Hepatology|May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fastingLaura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 27, 2010
Impaired glucose tolerance in patients with amyotrophic lateral sclerosisPierre-Francois Pradat, Gaelle Bruneteau, Paul H Gordon, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
Plos Genetics|March 28, 2015
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesisAymeric Chartier, Pierre Klein, Stéphanie Pierson, et al.
Pageof 6