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Pascal Reynier

Showing results (111-120 of 245) with videos related to

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Analytical Chemistry|December 20, 2016
A Nontargeted UHPLC-HRMS Metabolomics Pipeline for Metabolite Identification: Application to Cardiac Remote Ischemic PreconditioningJudith Kouassi Nzoughet, Cinzia Bocca, Gilles Simard, et al.
Journal of Clinical Medicine|July 9, 2020
Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed EntityXavier Dieu, Nathalie Bouzamondo, Claire Briet, et al.
Brain : a Journal of Neurology|November 1, 2022
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probandsAude Rocatcher, Valérie Desquiret-Dumas, Majida Charif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathyCédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Human Mutation|November 27, 2021
NR2F1 database: 112 variants and 84 patients support refining the clinical synopsis of Bosch-Boonstra-Schaaf optic atrophy syndromeBenjamin Billiet, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, et al.
The Ocular Surface|July 31, 2021
Tear metabolomics highlights new potential biomarkers for differentiating between Sjögren's syndrome and other causes of dry eyeGeoffrey Urbanski, Sophie Assad, Floris Chabrun, et al.
Cell Reports|February 24, 2015
A mitochondria-specific isoform of FASTK is present in mitochondrial RNA granules and regulates gene expression and functionAlexis A Jourdain, Mirko Koppen, Christopher D Rodley, et al.
Annales D'Endocrinologie|October 9, 2019
Apparent resistance to thyroid hormones: From biological interference to geneticsXavier Dieu, Guillaume Sueur, Valérie Moal, et al.
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.
Pageof 25

Showing results (111-120 of 245) with videos related to

Sort By:
Pageof 25
Analytical Chemistry|December 20, 2016
A Nontargeted UHPLC-HRMS Metabolomics Pipeline for Metabolite Identification: Application to Cardiac Remote Ischemic PreconditioningJudith Kouassi Nzoughet, Cinzia Bocca, Gilles Simard, et al.
Journal of Clinical Medicine|July 9, 2020
Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed EntityXavier Dieu, Nathalie Bouzamondo, Claire Briet, et al.
Brain : a Journal of Neurology|November 1, 2022
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probandsAude Rocatcher, Valérie Desquiret-Dumas, Majida Charif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathyCédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Human Mutation|November 27, 2021
NR2F1 database: 112 variants and 84 patients support refining the clinical synopsis of Bosch-Boonstra-Schaaf optic atrophy syndromeBenjamin Billiet, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, et al.
The Ocular Surface|July 31, 2021
Tear metabolomics highlights new potential biomarkers for differentiating between Sjögren's syndrome and other causes of dry eyeGeoffrey Urbanski, Sophie Assad, Floris Chabrun, et al.
Cell Reports|February 24, 2015
A mitochondria-specific isoform of FASTK is present in mitochondrial RNA granules and regulates gene expression and functionAlexis A Jourdain, Mirko Koppen, Christopher D Rodley, et al.
Annales D'Endocrinologie|October 9, 2019
Apparent resistance to thyroid hormones: From biological interference to geneticsXavier Dieu, Guillaume Sueur, Valérie Moal, et al.
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.
Pageof 25