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Marc Ferré

Showing results (31-40 of 40) with videos related to

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Brain : a Journal of Neurology|July 12, 2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Dominique Bonneau, Estelle Colin, Florine Oca, et al.
Journal of Clinical Medicine|March 4, 2020
A Plasma Metabolomic Profiling of Exudative Age-Related Macular Degeneration Showing Carnosine and Mitochondrial DeficienciesJuan M Chao de la Barca, Barnabé Rondet-Courbis, Marc Ferré, et al.
Nature Communications|June 30, 2023
Author Correction: Endogenous IL-1 receptor antagonist restricts healthy and malignant myeloproliferationAlicia Villatoro, Vincent Cuminetti, Aurora Bernal, et al.
Nature Communications|January 3, 2023
Endogenous IL-1 receptor antagonist restricts healthy and malignant myeloproliferationAlicia Villatoro, Vincent Cuminetti, Aurora Bernal, 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.
American Journal of Human Genetics|December 4, 2014
Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndromeEstelle Colin, Evelyne Huynh Cong, Géraldine Mollet, 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.
Nature Communications|February 5, 2026
Succinate receptor 1 restricts hematopoiesis and prevents acute myeloid leukemia progressionVincent Cuminetti, Emeline Boet, Marcel Heugel, et al.
JAMA Ophthalmology|April 9, 2026
Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic AtrophyCléis Beaulieu, Aymane Bouzidi, Valérie Desquiret-Dumas, et al.
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Brain : a Journal of Neurology|July 12, 2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Dominique Bonneau, Estelle Colin, Florine Oca, et al.
Journal of Clinical Medicine|March 4, 2020
A Plasma Metabolomic Profiling of Exudative Age-Related Macular Degeneration Showing Carnosine and Mitochondrial DeficienciesJuan M Chao de la Barca, Barnabé Rondet-Courbis, Marc Ferré, et al.
Nature Communications|June 30, 2023
Author Correction: Endogenous IL-1 receptor antagonist restricts healthy and malignant myeloproliferationAlicia Villatoro, Vincent Cuminetti, Aurora Bernal, et al.
Nature Communications|January 3, 2023
Endogenous IL-1 receptor antagonist restricts healthy and malignant myeloproliferationAlicia Villatoro, Vincent Cuminetti, Aurora Bernal, 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.
American Journal of Human Genetics|December 4, 2014
Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndromeEstelle Colin, Evelyne Huynh Cong, Géraldine Mollet, 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.
Nature Communications|February 5, 2026
Succinate receptor 1 restricts hematopoiesis and prevents acute myeloid leukemia progressionVincent Cuminetti, Emeline Boet, Marcel Heugel, et al.
JAMA Ophthalmology|April 9, 2026
Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic AtrophyCléis Beaulieu, Aymane Bouzidi, Valérie Desquiret-Dumas, et al.
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Pageof 4