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 *

255 related articles for article (PubMed ID: 24776766)

  • 1. Clinical severity of Gitelman syndrome determined by serum magnesium.
    Jiang L; Chen C; Yuan T; Qin Y; Hu M; Li X; Xing X; Lee X; Nie M; Chen L
    Am J Nephrol; 2014; 39(4):357-66. PubMed ID: 24776766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. NORMOMAGNESEMIC GITELMAN SYNDROME PATIENTS EXHIBIT A STRONGER REACTION TO THIAZIDE THAN HYPOMAGNESEMIC PATIENTS.
    Jiang L; Peng X; Ma J; Yuan T; Qin Y; Wang O; Wang H; Wang Y; Chen G; Yue C; Li C; Nie M; Xing X; Li X; Lee X; Chen L
    Endocr Pract; 2015 Sep; 21(9):1017-25. PubMed ID: 26121437
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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; 21(1):328. PubMed ID: 32758178
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome.
    Peng X; Jiang L; Chen C; Qin Y; Yuan T; Wang O; Xing X; Li X; Nie M; Chen L
    PLoS One; 2017; 12(7):e0180811. PubMed ID: 28700713
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome.
    Balavoine AS; Bataille P; Vanhille P; Azar R; Noël C; Asseman P; Soudan B; Wémeau JL; Vantyghem MC
    Eur J Endocrinol; 2011 Oct; 165(4):665-73. PubMed ID: 21753071
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Expert consensus for the diagnosis and treatment of patients with Gitelman syndrome].
    Gitelman Syndrome Collaborative Study Group
    Zhonghua Nei Ke Za Zhi; 2017 Sep; 56(9):712-716. PubMed ID: 28870047
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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; 99(5):474-480. PubMed ID: 36562655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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; 23(1):170. PubMed ID: 35509038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 102(24):e33959. PubMed ID: 37327293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A pedigree analysis of two homozygous mutant Gitelman syndrome cases.
    Luo J; Yang X; Liang J; Li W
    Endocr J; 2015; 62(1):29-36. PubMed ID: 25273610
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemia.
    Nakamura A; Shimizu C; Nagai S; Yoshida M; Aoki K; Kondo T; Miyoshi H; Wada N; Tajima T; Terauchi Y; Yoshioka N; Koike T
    Clin Endocrinol (Oxf); 2010 Feb; 72(2):272-6. PubMed ID: 19508680
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
    Blanchard A; Bockenhauer D; Bolignano D; Calò LA; Cosyns E; Devuyst O; Ellison DH; Karet Frankl FE; Knoers NV; Konrad M; Lin SH; Vargas-Poussou R
    Kidney Int; 2017 Jan; 91(1):24-33. PubMed ID: 28003083
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Gitelman´s syndrome as common cause of hypokalemia and hypomagnesemia].
    Ryšavá R; Reiterová J; Urbanová M; Štekrová J; Lněnička P; Tesař V
    Vnitr Lek; 2016; 62 Suppl 6():78-83. PubMed ID: 28124936
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 6(1):37-9. PubMed ID: 23282232
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome.
    Liu T; Wang C; Lu J; Zhao X; Lang Y; Shao L
    Am J Nephrol; 2016; 44(2):159-68. PubMed ID: 27529443
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simultaneous Homozygous Mutations in
    Mou L; Wu F
    Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33807568
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.