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Pascal Reynier

Showing results (221-230 of 245) with videos related to

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Scientific Reports|August 12, 2025
Machine learning-assisted quantitative metabolomics of West African patients with advanced breast cancerAboubacar Dit Tietie Bissan, Mathieu Michel, Xavier Dieu, et al.
Investigative Ophthalmology & Visual Science|February 5, 2017
Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ MiceJuan Manuel Chao de la Barca, Gilles Simard, Emmanuelle Sarzi, et al.
Biomedicines|July 27, 2022
Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body ExposureSophie Belal, David Goudenège, Cinzia Bocca, et al.
Antioxidants (Basel, Switzerland)|January 22, 2024
A Metabolomic Signature of Ischemic Stroke Showing Acute Oxidative and Energetic StressMoustapha Djite, Juan Manuel Chao de la Barca, Cinzia Bocca, et al.
Brain : a Journal of Neurology|March 13, 2018
Reply: The expanding neurological phenotype of DNM1L-related disordersSylvie Gerber, Majida Charif, Arnaud Chevrollier, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chipMarianne Lévêque, Sandrine Marlin, Laurence Jonard, et al.
Brain : a Journal of Neurology|September 17, 2016
The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stressJuan Manuel Chao de la Barca, Gilles Simard, Patrizia Amati-Bonneau, et al.
Plos One|August 11, 2012
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathyAlessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
Brain : a Journal of Neurology|October 4, 2017
Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fissionSylvie Gerber, Majida Charif, Arnaud Chevrollier, et al.
Autoimmunity Reviews|June 10, 2018
Primary antiphospholipid syndrome and antiphospholipid syndrome associated to systemic lupus: Are they different entities?Cristina Belizna, Ljudmila Stojanovich, Jan Willem Cohen-Tervaert, et al.
Pageof 25

Showing results (221-230 of 245) with videos related to

Sort By:
Pageof 25
Scientific Reports|August 12, 2025
Machine learning-assisted quantitative metabolomics of West African patients with advanced breast cancerAboubacar Dit Tietie Bissan, Mathieu Michel, Xavier Dieu, et al.
Investigative Ophthalmology & Visual Science|February 5, 2017
Targeted Metabolomics Reveals Early Dominant Optic Atrophy Signature in Optic Nerves of Opa1delTTAG/+ MiceJuan Manuel Chao de la Barca, Gilles Simard, Emmanuelle Sarzi, et al.
Biomedicines|July 27, 2022
Glutamate-Induced Deregulation of Krebs Cycle in Mitochondrial Encephalopathy Lactic Acidosis Syndrome Stroke-Like Episodes (MELAS) Syndrome Is Alleviated by Ketone Body ExposureSophie Belal, David Goudenège, Cinzia Bocca, et al.
Antioxidants (Basel, Switzerland)|January 22, 2024
A Metabolomic Signature of Ischemic Stroke Showing Acute Oxidative and Energetic StressMoustapha Djite, Juan Manuel Chao de la Barca, Cinzia Bocca, et al.
Brain : a Journal of Neurology|March 13, 2018
Reply: The expanding neurological phenotype of DNM1L-related disordersSylvie Gerber, Majida Charif, Arnaud Chevrollier, et al.
European Journal of Human Genetics : EJHG|July 20, 2007
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chipMarianne Lévêque, Sandrine Marlin, Laurence Jonard, et al.
Brain : a Journal of Neurology|September 17, 2016
The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stressJuan Manuel Chao de la Barca, Gilles Simard, Patrizia Amati-Bonneau, et al.
Plos One|August 11, 2012
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathyAlessandro Achilli, Luisa Iommarini, Anna Olivieri, et al.
Brain : a Journal of Neurology|October 4, 2017
Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fissionSylvie Gerber, Majida Charif, Arnaud Chevrollier, et al.
Autoimmunity Reviews|June 10, 2018
Primary antiphospholipid syndrome and antiphospholipid syndrome associated to systemic lupus: Are they different entities?Cristina Belizna, Ljudmila Stojanovich, Jan Willem Cohen-Tervaert, et al.
Pageof 25