These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 28685938)

  • 1. Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review.
    Gu X; Su Z; Chen M; Xu Y; Wang Y
    Nephrology (Carlton); 2017 Aug; 22(8):652-655. PubMed ID: 28685938
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Acquired Gitelman syndrome in a patient with primary Sjögren syndrome.
    Kim YK; Song HC; Kim WY; Yoon HE; Choi YJ; Ki CS; Park CW; Yang CW; Kim J; Kim YS; Choi EJ; Bang BK
    Am J Kidney Dis; 2008 Dec; 52(6):1163-7. PubMed ID: 18805608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gitelman's syndrome with vomiting manifested by severe metabolic alkalosis and progressive renal insufficiency.
    Lee JH; Lee J; Han JS
    Tohoku J Exp Med; 2013 Nov; 231(3):165-9. PubMed ID: 24162365
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Quadriparesis due to Gitelman's syndrome diagnosed with thiazide diuretic test response.
    Mukhopadhyay S; Jana S; Chatterjee A; Roy M; Sarkar A; Mukhopadhyay J
    Saudi J Kidney Dis Transpl; 2016 Mar; 27(2):407-10. PubMed ID: 26997401
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.
    Yang W; Zhao S; Xie Y; Mo Z
    BMC Nephrol; 2018 Dec; 19(1):362. PubMed ID: 30558554
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation.
    Kusuda T; Hosoya T; Mori T; Ihara K; Nishida H; Chiga M; Sohara E; Rai T; Koike R; Uchida S; Kohsaka H
    Intern Med; 2016; 55(21):3201-3204. PubMed ID: 27803420
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A NOVEL COMPOUND HETEROZYGOUS VARIANT OF SLC12A3 GENE IN A PEDIGREE WITH GITELMAN SYNDROME CO-EXISTENT WITH THYROID DYSFUNCTION.
    Liu S; Ke J; Zhang B; Yu C; Feng Y; Zhao D
    Endocr Pract; 2018 Oct; 24(10):889-893. PubMed ID: 30084681
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gitelman syndrome in a South African family presenting with hypokalaemia and unusual food cravings.
    van der Merwe PD; Rensburg MA; Haylett WL; Bardien S; Davids MR
    BMC Nephrol; 2017 Jan; 18(1):38. PubMed ID: 28125972
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous
    Zhang JH; Ruan DD; Hu YN; Ruan XL; Zhu YB; Yang X; Wu JB; Lin XF; Luo JW; Tang FQ
    Biomed Res Int; 2021; 2021():9973161. PubMed ID: 34046503
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 14(1):198. PubMed ID: 34348722
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 31(1):47-54. PubMed ID: 26770037
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 19(1):114. PubMed ID: 30999883
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel SLC12A3 mutation in Gitelman syndrome.
    Veríssimo R; Leite de Sousa L; Carvalho TJ; Fidalgo P
    BMJ Case Rep; 2021 Jan; 14(1):. PubMed ID: 33462018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A rare case of Gitelman's syndrome with hypophosphatemia.
    Akhtar N; Hafeez F
    J Coll Physicians Surg Pak; 2009 Apr; 19(4):257-9. PubMed ID: 19356345
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gitelman's syndrome: towards genotype-phenotype correlations?
    Riveira-Munoz E; Chang Q; Bindels RJ; Devuyst O
    Pediatr Nephrol; 2007 Mar; 22(3):326-32. PubMed ID: 17061123
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 19(1):17. PubMed ID: 29378538
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel compound heterozygous mutation of Gitelman's syndrome in Japan, as diagnosed by an extraordinary response of the fractional excretion rate of chloride in the trichlormethiazide loading test.
    Ueda K; Makita N; Kawarazaki H; Fujiwara T; Unuma S; Monkawa T; Hayashi M; Fujita T
    Intern Med; 2012; 51(12):1549-53. PubMed ID: 22728489
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypokalaemic paralysis and metabolic alkalosis in a patient with Sjögren syndrome: a case report and literature review.
    Ranaweerage R; Perera S; Gunapala A
    BMC Nephrol; 2021 Apr; 22(1):159. PubMed ID: 33931020
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 31(1):259-262. PubMed ID: 32129221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 42(9):1035-1040. PubMed ID: 32712837
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.