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Amino acids and vitamins status during continuous renal replacement therapy: An ancillary prospective observational study of a randomised control trial.
Schneider AG, Picard W, Honoré PM, Dewitte A, Mesli S, Redonnet-Vernhet I, Fleureau C, Ouattara A, Berger MM, Joannes-Boyau O. Schneider AG, et al. Among authors: mesli s. Anaesth Crit Care Pain Med. 2021 Apr;40(2):100813. doi: 10.1016/j.accpm.2021.100813. Epub 2021 Feb 12. Anaesth Crit Care Pain Med. 2021. PMID: 33588088 Clinical Trial.
Adult-onset diagnosis of urea cycle disorders: Results of a French cohort of 71 patients.
Toquet S, Spodenkiewicz M, Douillard C, Maillot F, Arnoux JB, Damaj L, Odent S, Moreau C, Redonnet-Vernhet I, Mesli S, Servais A, Noel E, Charriere S, Rigalleau V, Lavigne C, Kaphan E, Roubertie A, Besson G, Bigot A, Servettaz A, Mochel F, Garnotel R. Toquet S, et al. Among authors: mesli s. J Inherit Metab Dis. 2021 Sep;44(5):1199-1214. doi: 10.1002/jimd.12403. Epub 2021 Jun 7. J Inherit Metab Dis. 2021. PMID: 34014557
[Review of nutritional components in Covid-19: what about micronutrients?].
Bost M, Richard E, Redonnet-Vernhet I, Parant F, Boulet L, Dupré T, Collin-Chavagnac D, Mesli S, Beauvieux MC; Groupe de Travail de la SFBC « Marqueurs biochimiques de Covid-19 ». Bost M, et al. Among authors: mesli s. Ann Biol Clin (Paris). 2022 Jul 1;80(4):319-331. doi: 10.1684/abc.2022.1741. Ann Biol Clin (Paris). 2022. PMID: 36099350 Review. French.
Preventing hyperhomocysteinemia using vitamin B6 supplementation in Givosiran-treated acute intermittent porphyria: Highlights from a case report and brief literature review.
Redonnet-Vernhet I, Mercié P, Lebreton L, Blouin JM, Bronnimann D, Mesli S, Guibet C, Ribeiro E, Gensous N, Duffau P, Gouya L, Richard E. Redonnet-Vernhet I, et al. Among authors: mesli s. Mol Genet Metab Rep. 2024 Apr 4;39:101076. doi: 10.1016/j.ymgmr.2024.101076. eCollection 2024 Jun. Mol Genet Metab Rep. 2024. PMID: 38601120 Free PMC article.
Case report: Unveiling genetic and phenotypic variability in Nonketotic hyperglycinemia: an atypical early onset case associated with a novel GLRX5 variant.
Marin V, Lebreton L, Guibet C, Mesli S, Redonnet-Vernhet I, Dexant M, Lamireau D, Roche S, Gaschignard M, Delmas J, Margot H, Bar C. Marin V, et al. Among authors: mesli s. Front Genet. 2024 Sep 11;15:1432272. doi: 10.3389/fgene.2024.1432272. eCollection 2024. Front Genet. 2024. PMID: 39323869 Free PMC article.
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.
Carrozzo R, Verrigni D, Rasmussen M, de Coo R, Amartino H, Bianchi M, Buhas D, Mesli S, Naess K, Born AP, Woldseth B, Prontera P, Batbayli M, Ravn K, Joensen F, Cordelli DM, Santorelli FM, Tulinius M, Darin N, Duno M, Jouvencel P, Burlina A, Stangoni G, Bertini E, Redonnet-Vernhet I, Wibrand F, Dionisi-Vici C, Uusimaa J, Vieira P, Osorio AN, McFarland R, Taylor RW, Holme E, Ostergaard E. Carrozzo R, et al. Among authors: mesli s. J Inherit Metab Dis. 2016 Mar;39(2):243-52. doi: 10.1007/s10545-015-9894-9. Epub 2015 Oct 16. J Inherit Metab Dis. 2016. PMID: 26475597
39 results