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Vincent Procaccio

Showing results (81-90 of 197) with videos related to

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Frontiers in Psychiatry|April 25, 2022
Neuropsychological Features of Children and Adolescents With Mitochondrial Disorders: A Descriptive Case SeriesElise Riquin, Magalie Barth, Thomas Le Nerzé, et al.
Frontiers in Psychiatry|August 6, 2021
Psychiatric Symptoms of Children and Adolescents With Mitochondrial Disorders: A Descriptive Case SeriesElise Riquin, Thomas Le Nerzé, Natwin Pasquini, et al.
Molecular Vision|March 28, 2009
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defectYannick Nochez, Sophie Arsene, Naig Gueguen, et al.
Annals of Clinical and Translational Neurology|July 26, 2023
Infantile-onset parkinsonism, dyskinesia, and developmental delay: do not forget polyglutamine defects!Heidy Baide-Mairena, Arthur Coget, Nicolas Leboucq, et al.
Molecular Neurodegeneration|February 26, 2021
Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathyMajida Charif, Yvette C Wong, Soojin Kim, et al.
Frontiers in Endocrinology|June 7, 2024
Ketogenic diet enhances the anti-cancer effects of PD-L1 blockade in renal cell carcinomaJeremy Richard, Céline Beauvillain, Maxime Benoit, et al.
Journal of Gynecology Obstetrics and Human Reproduction|February 7, 2020
The cytokine profile of follicular fluid changes during ovarian ageingPierre-Emmanuel Bouet, Thomas Boueilh, Juan Manuel Chao de la Barca, et al.
Progress in Neurobiology|September 27, 2019
Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in miceFloris Chabrun, Xavier Dieu, Guillaume Rousseau, et al.
Annales De Biologie Clinique|February 15, 2021
[Usefulness of combined sequencing of the mitochondrial genome and a targeted panel of nuclear genes involved in mitochondrial diseases]Benoit Rucheton, Flavie Ader, David Goudenege, et al.
Brain : a Journal of Neurology|December 23, 2011
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotypeCécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Pageof 20

Showing results (81-90 of 197) with videos related to

Sort By:
Pageof 20
Frontiers in Psychiatry|April 25, 2022
Neuropsychological Features of Children and Adolescents With Mitochondrial Disorders: A Descriptive Case SeriesElise Riquin, Magalie Barth, Thomas Le Nerzé, et al.
Frontiers in Psychiatry|August 6, 2021
Psychiatric Symptoms of Children and Adolescents With Mitochondrial Disorders: A Descriptive Case SeriesElise Riquin, Thomas Le Nerzé, Natwin Pasquini, et al.
Molecular Vision|March 28, 2009
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defectYannick Nochez, Sophie Arsene, Naig Gueguen, et al.
Annals of Clinical and Translational Neurology|July 26, 2023
Infantile-onset parkinsonism, dyskinesia, and developmental delay: do not forget polyglutamine defects!Heidy Baide-Mairena, Arthur Coget, Nicolas Leboucq, et al.
Molecular Neurodegeneration|February 26, 2021
Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathyMajida Charif, Yvette C Wong, Soojin Kim, et al.
Frontiers in Endocrinology|June 7, 2024
Ketogenic diet enhances the anti-cancer effects of PD-L1 blockade in renal cell carcinomaJeremy Richard, Céline Beauvillain, Maxime Benoit, et al.
Journal of Gynecology Obstetrics and Human Reproduction|February 7, 2020
The cytokine profile of follicular fluid changes during ovarian ageingPierre-Emmanuel Bouet, Thomas Boueilh, Juan Manuel Chao de la Barca, et al.
Progress in Neurobiology|September 27, 2019
Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in miceFloris Chabrun, Xavier Dieu, Guillaume Rousseau, et al.
Annales De Biologie Clinique|February 15, 2021
[Usefulness of combined sequencing of the mitochondrial genome and a targeted panel of nuclear genes involved in mitochondrial diseases]Benoit Rucheton, Flavie Ader, David Goudenege, et al.
Brain : a Journal of Neurology|December 23, 2011
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotypeCécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Pageof 20