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Dominique Bonneau

Showing results (91-100 of 253) with videos related to

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Neurology. Genetics|December 22, 2017
Novel <i>NDUFS4</i> gene mutation in an atypical late-onset mitochondrial form of multifocal dystoniaCeline Bris, Tiphaine Rouaud, Valerie Desquiret-Dumas, et al.
Journal of Cellular and Molecular Medicine|April 6, 2017
Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophyMariame Selma Kane, Jennifer Alban, Valérie Desquiret-Dumas, et al.
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.
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.
Neuropsychologia|June 10, 2011
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's diseasePhilippe Allain, Véronique Gaura, Luciano Fasotti, 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.
Hormone Research in Paediatrics|May 27, 2020
Hypopituitarism in Patients with Blepharophimosis and FOXL2 MutationsSarah Castets, Florence Roucher-Boulez, Alexandru Saveanu, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2026
COQ7-Related Neuropathy: Two New Cases and Review of the LiteratureJulian Theuriet, Shams Ribault, Fanny Fontaine, et al.
Journal of Cellular Physiology|December 15, 2006
Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesisAurélien Olichon, Thomas Landes, Laetitia Arnauné-Pelloquin, 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.
Pageof 26

Showing results (91-100 of 253) with videos related to

Sort By:
Pageof 26
Neurology. Genetics|December 22, 2017
Novel <i>NDUFS4</i> gene mutation in an atypical late-onset mitochondrial form of multifocal dystoniaCeline Bris, Tiphaine Rouaud, Valerie Desquiret-Dumas, et al.
Journal of Cellular and Molecular Medicine|April 6, 2017
Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophyMariame Selma Kane, Jennifer Alban, Valérie Desquiret-Dumas, et al.
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.
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.
Neuropsychologia|June 10, 2011
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's diseasePhilippe Allain, Véronique Gaura, Luciano Fasotti, 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.
Hormone Research in Paediatrics|May 27, 2020
Hypopituitarism in Patients with Blepharophimosis and FOXL2 MutationsSarah Castets, Florence Roucher-Boulez, Alexandru Saveanu, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2026
COQ7-Related Neuropathy: Two New Cases and Review of the LiteratureJulian Theuriet, Shams Ribault, Fanny Fontaine, et al.
Journal of Cellular Physiology|December 15, 2006
Effects of OPA1 mutations on mitochondrial morphology and apoptosis: relevance to ADOA pathogenesisAurélien Olichon, Thomas Landes, Laetitia Arnauné-Pelloquin, 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.
Pageof 26