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 *

169 related articles for article (PubMed ID: 37138571)

  • 1. A mosaic mutation in the
    Zhou L; Chen X; Xiong J; Lei L
    Front Pediatr; 2023; 11():1034923. PubMed ID: 37138571
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report.
    Zhu B; Jiang H; Cao M; Zhao X; Jiang H
    BMC Med Genet; 2019 Aug; 20(1):137. PubMed ID: 31409296
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis.
    Zhao Q; Xiang Q; Tan Y; Xiao X; Xie H; Wang H; Yang M; Liu S
    Mol Genet Genomic Med; 2022 Oct; 10(10):e2027. PubMed ID: 35913199
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel homozygous CLCNKB variant: An early presentation of classic Bartter syndrome in a neonate.
    Yaprak D; Kara H; Calisici E; Karagöl BS; Altan M
    Birth Defects Res; 2023 Oct; 115(17):1674-1679. PubMed ID: 37587715
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Chinese Girl with Bartter Syndrome Type III due to a Novel Mutation and/or Single Nucleotide Polymorphisms (SNPs) in CLCNKB Gene.
    Xiumin W; Zheng S; Meichun X; Junfen F; Li L
    Iran J Pediatr; 2013 Feb; 23(1):89-94. PubMed ID: 23550235
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation of
    Cho HW; Lee ST; Cho H; Cheong HI
    Korean J Pediatr; 2016 Nov; 59(Suppl 1):S103-S106. PubMed ID: 28018459
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Adult classic Bartter syndrome: a case report with 5-year follow-up and literature review.
    Jiang L; Li D; Guo Q; Li Y; Zan L; Ao R
    Endocr J; 2024 May; 71(5):537-542. PubMed ID: 38508775
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome.
    Yu Y; Xu C; Pan X; Ren H; Wang W; Meng X; Huang F; Chen N
    Clin Genet; 2010 Feb; 77(2):155-62. PubMed ID: 19807735
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Splicing Characterization of
    Wang C; Han Y; Zhou J; Zheng B; Zhou W; Bao H; Jia Z; Zhang A; Huang S; Ding G; Zhao F
    Front Genet; 2020; 11():81. PubMed ID: 32153641
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in
    Tian M; Peng H; Bi X; Wang YQ; Zhang YZ; Wu Y; Zhang BR
    Front Med (Lausanne); 2022; 9():862514. PubMed ID: 35463019
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bartter syndrome with long-term follow-up: a case report.
    Wu X; Yang G; Chen S; Tang M; Jian S; Chen F; Wu X
    J Int Med Res; 2020 Aug; 48(8):300060520947876. PubMed ID: 32857947
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A New Case Report of a CLCNKB Complex Heterozygous Mutation in Adult-Onset Type III Bartter Syndrome.
    Chen G; Hong P
    Clin Lab; 2024 Aug; 70(8):. PubMed ID: 39193977
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
    Andrini O; Keck M; Briones R; Lourdel S; Vargas-Poussou R; Teulon J
    Am J Physiol Renal Physiol; 2015 Jun; 308(12):F1324-34. PubMed ID: 25810436
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.
    Cheng CJ; Lo YF; Chen JC; Huang CL; Lin SH
    J Physiol; 2017 Aug; 595(16):5573-5586. PubMed ID: 28555925
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.
    Konrad M; Vollmer M; Lemmink HH; VAN DEN Heuvel LPWJ; Jeck N; Vargas-Poussou R; Lakings A; Ruf R; Deschênes G; Antignac C; Guay-Woodford L; Knoers NVAM; Seyberth HW; Feldmann D; Hildebrandt F
    J Am Soc Nephrol; 2000 Aug; 11(8):1449-1459. PubMed ID: 10906158
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel compound heterozygous CLCNKB gene mutations (c.1755A>G/c.848_850delTCT) cause classic Bartter syndrome.
    Wang C; Chen Y; Zheng B; Zhu M; Fan J; Wang J; Jia Z; Huang S; Zhang A
    Am J Physiol Renal Physiol; 2018 Oct; 315(4):F844-F851. PubMed ID: 29442545
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome.
    Hernández NEG; Pérez LIE; Aguilera D; Camargo-Muñiz MD; Espinosa CFC; Jaramillo MCR; Salvador C; González ZL; Hureaux M; Vargas-Poussou R
    Arch Med Res; 2023 Sep; 54(6):102859. PubMed ID: 37516009
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome.
    Bettinelli A; Borsa N; Syrén ML; Mattiello C; Coviello D; Edefonti A; Giani M; Travi M; Tedeschi S
    Pediatr Res; 2005 Dec; 58(6):1269-73. PubMed ID: 16306206
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome.
    Chiang WF; Lin SH; Chan JS; Lin SH
    Clin Nephrol; 2014 Feb; 81(2):146-50. PubMed ID: 22854165
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.