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 *

285 related articles for article (PubMed ID: 31285285)

  • 21. Genetic Analysis of Gitelman Syndrome: Co-existence with Hyperthyroidism in a Two-year-old Boy.
    Yu S; Wang C
    Endocr Metab Immune Disord Drug Targets; 2021; 21(8):1524-1530. PubMed ID: 33121425
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.
    Viering D; Schlingmann KP; Hureaux M; Nijenhuis T; Mallett A; Chan MMY; van Beek A; van Eerde AM; Coulibaly JM; Vallet M; Decramer S; Pelletier S; Klaus G; Kömhoff M; Beetz R; Patel C; Shenoy M; Steenbergen EJ; Anderson G; Bongers EMHF; Bergmann C; Panneman D; Rodenburg RJ; Kleta R; Houillier P; Konrad M; Vargas-Poussou R; Knoers NVAM; Bockenhauer D; de Baaij JHF;
    J Am Soc Nephrol; 2022 Feb; 33(2):305-325. PubMed ID: 34607911
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature.
    Koca O; Alay MT; Murt A; Kalayci Yigin A; Seven M; Bavunoglu I
    CEN Case Rep; 2024 Oct; 13(5):330-338. PubMed ID: 38308744
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genotype, phenotype, and follow-up in Taiwanese patients with salt-losing tubulopathy associated with SLC12A3 mutation.
    Tseng MH; Yang SS; Hsu YJ; Fang YW; Wu CJ; Tsai JD; Hwang DY; Lin SH
    J Clin Endocrinol Metab; 2012 Aug; 97(8):E1478-82. PubMed ID: 22679066
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Abnormal glucose metabolism and insulin sensitivity in Chinese patients with Gitelman syndrome.
    Ren H; Qin L; Wang W; Ma J; Zhang W; Shen PY; Shi H; Li X; Chen N
    Am J Nephrol; 2013; 37(2):152-7. PubMed ID: 23392128
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review.
    Xu J; He J; Xu S; Wang R; Peng N; Zhang M
    BMC Nephrol; 2023 May; 24(1):123. PubMed ID: 37131142
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Novel mutation in the SLC12A3 gene in a Sri Lankan family with Gitelman syndrome & coexistent diabetes: a case report.
    Subasinghe CJ; Sirisena ND; Herath C; Berge KE; Leren TP; Bulugahapitiya U; Dissanayake VHW
    BMC Nephrol; 2017 Apr; 18(1):140. PubMed ID: 28446151
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Sectio Caesarea under Gitelman Syndrome].
    Rombach S; Benner A; Schick MA
    Anasthesiol Intensivmed Notfallmed Schmerzther; 2021 Apr; 56(4):289-295. PubMed ID: 33890260
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 67(3):673-677. PubMed ID: 31808035
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases.
    Kondo A; Nagano C; Ishiko S; Omori T; Aoto Y; Rossanti R; Sakakibara N; Horinouchi T; Yamamura T; Nagai S; Okada E; Shima Y; Nakanishi K; Ninchoji T; Kaito H; Takeda H; Nagase H; Morisada N; Iijima K; Nozu K
    Sci Rep; 2021 Aug; 11(1):16099. PubMed ID: 34373523
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical and genetic analyses of Chinese patients with Gitelman syndrome.
    Miao M; Zhao CQ; Wang XL; Shan ZY
    Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173320
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Gitelman syndrome: an analysis of the underlying pathophysiologic mechanisms of acid-base and electrolyte abnormalities.
    Filippatos TD; Rizos CV; Tzavella E; Elisaf MS
    Int Urol Nephrol; 2018 Jan; 50(1):91-96. PubMed ID: 28744758
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene.
    Wolyniec W; Jakubowska SK; Nagel M; Wolyniec Z; Obolonczyk L; Swiatkowska-Stodulska R; Sworczak K; Renke M
    Nefrologia; 2016; 36(3):304-9. PubMed ID: 26306968
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus.
    Iio K; Mori T; Bessho S; Imai Y; Hatanaka M; Omori H; Kouhara H; Chiga M; Sohara E; Uchida S; Kaimori JY
    CEN Case Rep; 2022 May; 11(2):191-195. PubMed ID: 34617250
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.