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Journal Abstract Search

547 related items for PubMed ID: 28870047

  • 1.
    ; . PubMed ID:
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  • 3. Gitelman syndrome.
    Knoers NV, Levtchenko EN.
    Orphanet J Rare Dis; 2008 Jul 30; 3():22. PubMed ID: 18667063
    [Abstract] [Full Text] [Related]

  • 4. Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome.
    Lee JW, Lee J, Heo NJ, Cheong HI, Han JS.
    J Korean Med Sci; 2016 Jan 30; 31(1):47-54. PubMed ID: 26770037
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  • 6. Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathy.
    Nozu K, Yamamura T, Horinouchi T, Nagano C, Sakakibara N, Ishikura K, Hamada R, Morisada N, Iijima K.
    Pediatr Int; 2020 Apr 30; 62(4):428-437. PubMed ID: 31830341
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  • 7. 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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  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Gitelman syndrome as a cause of psychomotor retardation in a toddler.
    Skalova S, Neuman D, Lnenicka P, Stekrova J.
    Arab J Nephrol Transplant; 2013 Jan 04; 6(1):37-9. PubMed ID: 23282232
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  • 11. [Bartter-Gitelman syndromes].
    Blanchard A, Courand PY, Livrozet M, Vargas-Poussou R.
    Nephrol Ther; 2020 Jul 04; 16(4):233-243. PubMed ID: 32622651
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  • 12. 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 04; 99(5):474-480. PubMed ID: 36562655
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  • 13. 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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  • 14. Gitelman syndrome with normocalciuria - a case report.
    Flisiński M, Skalska E, Mączyńska B, Butt-Hussaim N, Sobczyńska-Tomaszewska A, Haus O, Manitius J.
    BMC Nephrol; 2022 May 04; 23(1):170. PubMed ID: 35509038
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  • 15. 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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  • 16. Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome.
    Kong Y, Xu K, Yuan K, Zhu J, Gu W, Liang L, Wang C.
    BMC Pediatr; 2019 Apr 18; 19(1):114. PubMed ID: 30999883
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  • 17. Renal calcium and magnesium handling in Gitelman syndrome.
    Reyes JV, Medina PMB.
    Am J Transl Res; 2022 Apr 18; 14(1):1-19. PubMed ID: 35173827
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  • 18.
    Parmar MS, Muppidi V, Bashir K.
    ; 2024 01 18. PubMed ID: 29083583
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  • 19. Persistent hypokalemia due to a rare mutation in gitelman's syndrome.
    Mamalis D, Stratigou T, Vallianou NG, Ioannidis GG, Apostolou T.
    Saudi J Kidney Dis Transpl; 2020 01 18; 31(1):259-262. PubMed ID: 32129221
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  • 20. A case report of Gitelman syndrome in children.
    Ying J, Wu H, Zhang R, Wu P, Sui F, Li Z.
    Medicine (Baltimore); 2023 Apr 14; 102(15):e33509. PubMed ID: 37058043
    [Abstract] [Full Text] [Related]

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