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Journal Abstract Search

184 related items for PubMed ID: 37058043

  • 1. 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]

  • 2. Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing.
    Yang L, Fan J, Liu Y, Ren Y, Liu Z, Fu H, Qi H, Yang J.
    Medicine (Baltimore); 2023 Jun 16; 102(24):e33959. PubMed ID: 37327293
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  • 3. 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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  • 4. 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 17; 6(1):37-9. PubMed ID: 23282232
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  • 5. Gitelman syndrome.
    Knoers NV, Levtchenko EN.
    Orphanet J Rare Dis; 2008 Jul 30; 3():22. PubMed ID: 18667063
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  • 6. Concurrent Gitelman Syndrome and Hyperthyroidism: Diagnostic Challenges in a 51-Year-Old Patient.
    Zhang Y, Yu H, Li J, Cheng L.
    Am J Case Rep; 2024 Aug 30; 25():e944909. PubMed ID: 39210578
    [Abstract] [Full Text] [Related]

  • 7. Clinical and genetic analysis of a case of Gitelman syndrome accompanied with Graves disease and adrenocortical adenoma: A case report.
    Qiao Y, Zhao J, Wu J, Cao L, Song G, Mao J.
    Medicine (Baltimore); 2024 Apr 12; 103(15):e37770. PubMed ID: 38608089
    [Abstract] [Full Text] [Related]

  • 8. Gitelman syndrome with primary hyperparathyroidism: A case report.
    Yu S, Sun J, Mou L.
    Medicine (Baltimore); 2024 Aug 23; 103(34):e39447. PubMed ID: 39183425
    [Abstract] [Full Text] [Related]

  • 9. 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 Aug 23; 31(1):259-262. PubMed ID: 32129221
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  • 13. 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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  • 15. Novel heterozygous mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome: A care-compliant case report.
    Bi Y, Kuang MY, Li ML.
    Medicine (Baltimore); 2023 Sep 01; 102(35):e34967. PubMed ID: 37657006
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  • 19. A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.
    Yang W, Zhao S, Xie Y, Mo Z.
    BMC Nephrol; 2018 Dec 17; 19(1):362. PubMed ID: 30558554
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  • 20. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.
    Zhang JH, Ruan DD, Hu YN, Ruan XL, Zhu YB, Yang X, Wu JB, Lin XF, Luo JW, Tang FQ.
    Biomed Res Int; 2021 Dec 17; 2021():9973161. PubMed ID: 34046503
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