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Claude Jardel

Showing results (1-10 of 52) with videos related to

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Annales De Pathologie|December 6, 2005
[Mitochondrial diseases: molecular mechanisms, clinical presentations and diagnosis investigations]Karine Auré, Claude Jardel, Anne Lombès
Biologie Aujourd'Hui|October 31, 2015
[Pathophysiology of human mitochondrial diseases]Anne Lombès, Karine Auré, Claude Jardel
Biochimie|August 27, 2013
Unsolved issues related to human mitochondrial diseasesAnne Lombès, Karine Auré, Christine Bellanné-Chantelot, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|June 29, 2016
Progressive Ataxia and Palatal Tremor: Think about POLG MutationsMarie Mongin, Cécile Delorme, Timothée Lenglet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 9, 2005
Soluble transferrin receptor in hemochromatosis patients during phlebotomy therapyLaurence Piéroni, Fatiha Mekhloufi, Jean-Marie Thiolières, et al.
Mitochondrion|February 24, 2018
Quantitative neuroimaging biomarkers in a series of 20 adult patients with POLG mutationsMarion Masingue, Isaac Adanyeguh, Maya Tchikviladzé, et al.
Brain : a Journal of Neurology|April 19, 2007
Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?Karine Auré, Hélène Ogier de Baulny, Pascal Laforêt, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 25, 2018
Adult-onset Generalized Dystonia as the Main Manifestation of MEGDEL SyndromeCamille Giron, Emmanuel Roze, Bertrand Degos, et al.
Gastroenterology|April 7, 2009
Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstructionAurélien Amiot, Maya Tchikviladzé, Francisca Joly, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 29, 2007
A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathySinda Mahjoub, Damien Sternberg, Rafik Boussaada, et al.
Pageof 6

Showing results (1-10 of 52) with videos related to

Sort By:
Pageof 6
Annales De Pathologie|December 6, 2005
[Mitochondrial diseases: molecular mechanisms, clinical presentations and diagnosis investigations]Karine Auré, Claude Jardel, Anne Lombès
Biologie Aujourd'Hui|October 31, 2015
[Pathophysiology of human mitochondrial diseases]Anne Lombès, Karine Auré, Claude Jardel
Biochimie|August 27, 2013
Unsolved issues related to human mitochondrial diseasesAnne Lombès, Karine Auré, Christine Bellanné-Chantelot, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|June 29, 2016
Progressive Ataxia and Palatal Tremor: Think about POLG MutationsMarie Mongin, Cécile Delorme, Timothée Lenglet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 9, 2005
Soluble transferrin receptor in hemochromatosis patients during phlebotomy therapyLaurence Piéroni, Fatiha Mekhloufi, Jean-Marie Thiolières, et al.
Mitochondrion|February 24, 2018
Quantitative neuroimaging biomarkers in a series of 20 adult patients with POLG mutationsMarion Masingue, Isaac Adanyeguh, Maya Tchikviladzé, et al.
Brain : a Journal of Neurology|April 19, 2007
Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression?Karine Auré, Hélène Ogier de Baulny, Pascal Laforêt, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|April 25, 2018
Adult-onset Generalized Dystonia as the Main Manifestation of MEGDEL SyndromeCamille Giron, Emmanuel Roze, Bertrand Degos, et al.
Gastroenterology|April 7, 2009
Frequency of mitochondrial defects in patients with chronic intestinal pseudo-obstructionAurélien Amiot, Maya Tchikviladzé, Francisca Joly, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 29, 2007
A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathySinda Mahjoub, Damien Sternberg, Rafik Boussaada, et al.
Pageof 6