Stéphane Allouche
4PUBLICATIONS
6CO-AUTHORS
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Publications (4)
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|Feb 27, 2026
Mitochondrial Dysfunctions in Human Primary Coenzyme Q10 Deficiencies.Fanny Fontaine, Romain Pénicaud, Stéphane Allouche
|Jun 27, 2025
Homozygous COQ9 mutation: a new cause of potentially treatable hereditary spastic paraplegia.Fanny Fontaine, Audrey Labalme, Chloé Laurencin
|Feb 24, 2021
Is plasma concentration of coenzyme Q10 a predictive marker for left ventricular remodelling after revascularization for ST-segment elevation myocardial infarction?Fanny Fontaine, Damien Legallois, Christian Créveuil
|Jun 29, 2019
Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome.Sarah Snanoudj, Patrick Mordel, Quentin Dupas
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