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2018 1
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2023 8
2024 1

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Page 1
Genome-wide analysis identifies MYH11 compound heterozygous variants leading to visceral myopathy corresponding to late-onset form of megacystis-microcolon-intestinal hypoperistalsis syndrome.
Billon C, Piccoli GB, de Sainte Agathe JM, Stoeva R, Derive N, Heidet L, Berrebi D, Bruneval P, Jeunemaitre X, Hureaux M. Billon C, et al. Among authors: hureaux m. Mol Genet Genomics. 2024 Apr 16;299(1):44. doi: 10.1007/s00438-024-02136-3. Mol Genet Genomics. 2024. PMID: 38625590
Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome.
Hernández NEG, Pérez LIE, Aguilera D, Camargo-Muñiz MD, Espinosa CFC, Jaramillo MCR, Salvador C, González ZL, Hureaux M, Vargas-Poussou R. Hernández NEG, et al. Among authors: hureaux m. Arch Med Res. 2023 Sep;54(6):102859. doi: 10.1016/j.arcmed.2023.102859. Epub 2023 Jul 27. Arch Med Res. 2023. PMID: 37516009
[Major advances in pediatric nephro-genetics].
Hureaux M, Heidet L, Vargas-Poussou R, Dorval G. Hureaux M, et al. Med Sci (Paris). 2023 Mar;39(3):234-245. doi: 10.1051/medsci/2023028. Epub 2023 Mar 21. Med Sci (Paris). 2023. PMID: 36943120 Free article. Review. French.
New advances in endocrine hypertension: from genes to biomarkers.
Fernandes-Rosa FL, Boulkroun S, Fedlaoui B, Hureaux M, Travers-Allard S, Drossart T, Favier J, Zennaro MC. Fernandes-Rosa FL, et al. Among authors: hureaux m. Kidney Int. 2023 Mar;103(3):485-500. doi: 10.1016/j.kint.2022.12.021. Epub 2023 Jan 13. Kidney Int. 2023. PMID: 36646167 Review.
Genetic basis of nephrogenic diabetes insipidus.
Hureaux M, Vargas-Poussou R. Hureaux M, et al. Mol Cell Endocrinol. 2023 Jan 15;560:111825. doi: 10.1016/j.mce.2022.111825. Epub 2022 Nov 30. Mol Cell Endocrinol. 2023. PMID: 36460218 Review.
Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman Syndrome.
Viering DHHM, Hureaux M, Neveling K, Latta F, Kwint M, Blanchard A, Konrad M, Bindels RJM, Schlingmann KP, Vargas-Poussou R, de Baaij JHF. Viering DHHM, et al. Among authors: hureaux m. J Am Soc Nephrol. 2023 Feb 1;34(2):333-345. doi: 10.1681/ASN.2022050627. Epub 2022 Nov 9. J Am Soc Nephrol. 2023. PMID: 36302598 Free PMC article.
Possible role for rare TRPM7 variants in patients with hypomagnesaemia with secondary hypocalcaemia.
Vargas-Poussou R, Claverie-Martin F, Prot-Bertoye C, Carotti V, van der Wijst J, Perdomo-Ramirez A, Fraga-Rodriguez GM, Hureaux M, Bos C, Latta F, Houillier P, Hoenderop JGJ, de Baaij JHF. Vargas-Poussou R, et al. Among authors: hureaux m. Nephrol Dial Transplant. 2023 Feb 28;38(3):679-690. doi: 10.1093/ndt/gfac182. Nephrol Dial Transplant. 2023. PMID: 35561741 Free PMC article.
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