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[Usefulness of combined sequencing of the mitochondrial genome and a targeted panel of nuclear genes involved in mitochondrial diseases].
Ann Biol Clin (Paris). 2021 Feb 1;79(1):28-40. doi: 10.1684/abc.2021.1621.
Ann Biol Clin (Paris). 2021.
PMID: 33586649
Free article.
French.
Homoplasmic deleterious MT-ATP6/8 mutations in adult patients.
Rucheton B, Jardel C, Filaut S, Amador MDM, Maisonobe T, Serre I, Romero NB, Leonard-Louis S, Haraux F, Lombès A.
Rucheton B, et al. Among authors: filaut s.
Mitochondrion. 2020 Nov;55:64-77. doi: 10.1016/j.mito.2020.08.004. Epub 2020 Aug 26.
Mitochondrion. 2020.
PMID: 32858252
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Homoplasmic mitochondrial tRNAPro mutation causing exercise-induced muscle swelling and fatigue.
Auré K, Fayet G, Chicherin I, Rucheton B, Filaut S, Heckel AM, Eichler J, Caillon F, Péréon Y, Entelis N, Tarassov I, Lombès A.
Auré K, et al. Among authors: filaut s.
Neurol Genet. 2020 Jul 15;6(4):e480. doi: 10.1212/NXG.0000000000000480. eCollection 2020 Aug.
Neurol Genet. 2020.
PMID: 32802947
Free PMC article.
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Severe respiratory complex III defect prevents liver adaptation to prolonged fasting.
Kremer LS, L'hermitte-Stead C, Lesimple P, Gilleron M, Filaut S, Jardel C, Haack TB, Strom TM, Meitinger T, Azzouz H, Tebib N, Ogier de Baulny H, Touati G, Prokisch H, Lombès A.
Kremer LS, et al. Among authors: filaut s.
J Hepatol. 2016 Aug;65(2):377-85. doi: 10.1016/j.jhep.2016.04.017. Epub 2016 May 2.
J Hepatol. 2016.
PMID: 27151179
Free PMC article.
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A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy.
Mahjoub S, Sternberg D, Boussaada R, Filaut S, Gmira F, Mechmech R, Jardel C, Arab SB.
Mahjoub S, et al. Among authors: filaut s.
Diagn Mol Pathol. 2007 Dec;16(4):238-42. doi: 10.1097/PDM.0b013e3180cc313b.
Diagn Mol Pathol. 2007.
PMID: 18043288
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