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 *

289 related articles for article (PubMed ID: 30084681)

  • 21. 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]  

  • 22. 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]  

  • 23. 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; 99(29):e21123. PubMed ID: 32702863
    [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. 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]  

  • 26. The first compound heterozygous mutations in SLC12A3 and PDX1 genes: a unique presentation of Gitelman syndrome with distinct insulin resistance and familial diabetes insights.
    Yin Y; Li L; Yu S; Xin Y; Zhu L; Hu X; Chen K; Gu W; Mu Y; Zang L; Lyu Z
    Front Endocrinol (Lausanne); 2023; 14():1327729. PubMed ID: 38333726
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Clinical and genetic characteristics of Gitelman syndrome in 5 pedigrees].
    Shi RR; Li CC; Fang L; Xu J; Guan QB; Zhou XL; Guo J; Han WX; Chen Q; Feng L; Zhao JJ; Xu C
    Zhonghua Nei Ke Za Zhi; 2017 Feb; 56(2):104-111. PubMed ID: 28162179
    [No Abstract]   [Full Text] [Related]  

  • 28. Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study.
    Blanchard A; Vallet M; Dubourg L; Hureaux M; Allard J; Haymann JP; de la Faille R; Arnoux A; Dinut A; Bergerot D; Becker PH; Courand PY; Baron S; Houillier P; Tack I; Devuyst O; Jeunemaitre X; Azizi M; Vargas-Poussou R
    J Am Soc Nephrol; 2019 Aug; 30(8):1534-1545. PubMed ID: 31285285
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family.
    Yagi H; Yahata K; Usui T; Hasegawa C; Seta K; Sugawara A
    Intern Med; 2011; 50(11):1211-4. PubMed ID: 21628937
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic analysis of the Gitelman syndrome coexisting with Osteogenesis imperfecta.
    Park SJ; Kim JY; Ahn HJ; Baik HW; Kang JH
    Clin Chim Acta; 2021 Jul; 518():116-122. PubMed ID: 33775700
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identification of two novel mutations in SLC12A3 gene in two Chinese pedigrees with Gitelman syndrome and review of literature.
    Li C; Zhou X; Han W; Jiang X; Liu J; Fang L; Wang H; Guan Q; Gao L; Zhao J; Xu J; Xu C
    Clin Endocrinol (Oxf); 2015 Dec; 83(6):985-93. PubMed ID: 25990047
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A novel heterozygous duplication of the
    Fanis P; Efstathiou E; Neocleous V; Phylactou LA; Hadjipanayis A
    J Genet; 2019 Mar; 98():. PubMed ID: 30945685
    [TBL] [Abstract][Full Text] [Related]  

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

  • 34. Analysis of mutations of two Gitelman syndrome family SLC12A3 genes and proposed treatments using Chinese medicine.
    Luo JW; Meng XR; Yang X; Liang JX; Hong FY; Zheng XY; Li WH
    Chin J Integr Med; 2017 Jun; 23(6):461-468. PubMed ID: 26825084
    [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. Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome.
    Lo YF; Nozu K; Iijima K; Morishita T; Huang CC; Yang SS; Sytwu HK; Fang YW; Tseng MH; Lin SH
    Clin J Am Soc Nephrol; 2011 Mar; 6(3):630-9. PubMed ID: 21051746
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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; 102(35):e34967. PubMed ID: 37657006
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome.
    Zhong F; Ying H; Jia W; Zhou X; Zhang H; Guan Q; Xu J; Fang L; Zhao J; Xu C
    J Endocrinol Invest; 2019 Jun; 42(6):653-665. PubMed ID: 30413979
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detecting pathogenic deep intronic variants in Gitelman syndrome.
    Rossanti R; Horinouchi T; Sakakibara N; Yamamura T; Nagano C; Ishiko S; Aoto Y; Kondo A; Nagai S; Awano H; Nagase H; Matsuo M; Iijima K; Nozu K
    Am J Med Genet A; 2022 Sep; 188(9):2576-2583. PubMed ID: 35785516
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Exonic mutations in the SLC12A3 gene cause exon skipping and premature termination in Gitelman syndrome.
    Takeuchi Y; Mishima E; Shima H; Akiyama Y; Suzuki C; Suzuki T; Kobayashi T; Suzuki Y; Nakayama T; Takeshima Y; Vazquez N; Ito S; Gamba G; Abe T
    J Am Soc Nephrol; 2015 Feb; 26(2):271-9. PubMed ID: 25060058
    [TBL] [Abstract][Full Text] [Related]  

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