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Journal Abstract Search

352 related items for PubMed ID: 34046503

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  • 2. Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes.
    Dong B, Chen Y, Liu X, Wang Y, Wang F, Zhao Y, Sun X, Zhao W.
    BMC Nephrol; 2020 Aug 05; 21(1):328. PubMed ID: 32758178
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  • 3. A pedigree analysis of two homozygous mutant Gitelman syndrome cases.
    Luo J, Yang X, Liang J, Li W.
    Endocr J; 2015 Aug 05; 62(1):29-36. PubMed ID: 25273610
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  • 5. A novel compound heterozygous mutation of SLC12A3 gene in a pedigree with Gitelman syndrome and literature review.
    Yang M, Dong Y, Tian J, Yan L, Chen Y, Qiu H, Liu W, Hu Y.
    Genes Genomics; 2020 Sep 05; 42(9):1035-1040. PubMed ID: 32712837
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  • 6. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree.
    Chen Y, Zhang Z, Lin X, Pan Q, Zheng F, Li H.
    BMC Med Genet; 2018 Jan 29; 19(1):17. PubMed ID: 29378538
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  • 7. A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene.
    Chen Q, Wu Y, Zhao J, Jia Y, Wang W.
    BMC Nephrol; 2018 Oct 19; 19(1):275. PubMed ID: 30340552
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  • 8. Gitelman syndrome and glomerular proteinuria: a link between loss of sodium-chloride cotransporter and podocyte dysfunction?
    Demoulin N, Aydin S, Cosyns JP, Dahan K, Cornet G, Auberger I, Loffing J, Devuyst O.
    Nephrol Dial Transplant; 2014 Sep 19; 29 Suppl 4():iv117-20. PubMed ID: 25165177
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  • 11. Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome.
    Ying Q, Ye Z, Zhang W, Pan Y, Dai L, Lin K, Feng X, Dong X, He F.
    Clin Endocrinol (Oxf); 2023 Nov 19; 99(5):474-480. PubMed ID: 36562655
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  • 14. A novel homozygous mutation (p.N958K) of SLC12A3 in Gitelman syndrome is associated with endoplasmic reticulum stress.
    Tang W, Huang X, Liu Y, Lv Q, Li T, Song Y, Zhang X, Chen X, Shi Y.
    J Endocrinol Invest; 2021 Mar 19; 44(3):471-480. PubMed ID: 32642858
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  • 16. A novel compound heterozygous mutation of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome.
    Wang X, Ding Y, Liu Q, Yang G.
    Endocrine; 2020 Mar 19; 67(3):673-677. PubMed ID: 31808035
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  • 17. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report.
    Liu Z, Wang S, Zhang R, Wang C, Lu J, Shao L.
    BMC Med Genomics; 2021 Aug 04; 14(1):198. PubMed ID: 34348722
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  • 18. Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome.
    Zhong F, Ying H, Jia W, Zhou X, Zhang H, Guan Q, Xu J, Fang L, Zhao J, Xu C.
    J Endocrinol Invest; 2019 Jun 04; 42(6):653-665. PubMed ID: 30413979
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  • 19. Type 2 diabetes mellitus caused by Gitelman syndrome-related hypokalemia: A case report.
    He G, Gang X, Sun Z, Wang P, Wang G, Guo W.
    Medicine (Baltimore); 2020 Jul 17; 99(29):e21123. PubMed ID: 32702863
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