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 *

245 related articles for article (PubMed ID: 29900164)

  • 1. Bartter Syndrome Type 3: Phenotype-Genotype Correlation and Favorable Response to Ibuprofen.
    Yang X; Zhang G; Wang M; Yang H; Li Q
    Front Pediatr; 2018; 6():153. PubMed ID: 29900164
    [No Abstract]   [Full Text] [Related]  

  • 2. Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes.
    Shaer AJ
    Am J Med Sci; 2001 Dec; 322(6):316-32. PubMed ID: 11780689
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical Course and Prognosis of Tubulopathies Characterized by Metabolic Alkalosis in Children.
    Huseynli B; Atmış B; Cevizli D; Bişgin A; Karabay Bayazıt A
    Turk Arch Pediatr; 2022 Nov; 57(6):644-650. PubMed ID: 36314956
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Thirteen novel CLCNKB variants and genotype/phenotype association study in 42 Chinese patients with Bartter syndrome type 3.
    Han Y; Cheng H; Shao S; Lang Y; Zhao X; Lin Y; Wang S; Shi X; Liu Z; Shao L
    Endocrine; 2020 Apr; 68(1):192-202. PubMed ID: 31834604
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation.
    Piao Y; Chen C; Wu D; Liu M; Li W; Chen J; Sang Y
    Mol Genet Metab Rep; 2024 Sep; 40():101112. PubMed ID: 39071140
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Antenatal Bartter Syndrome: A Case Report.
    Akther M; Moni SC; Jahan I; Shabuj KH; Dey SK; Mannan MA; Shahidullah M
    Mymensingh Med J; 2020 Apr; 29(2):469-472. PubMed ID: 32506108
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.
    Rodríguez-Soriano J; Vallo A; Pérez de Nanclares G; Bilbao JR; Castaño L
    Pediatr Nephrol; 2005 Jul; 20(7):891-6. PubMed ID: 15875219
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Bartter syndrome and pseudo-Bartter syndrome--a case report].
    Gläser V; Hallebach V; Hans S
    Z Urol Nephrol; 1986 Jan; 79(1):19-27. PubMed ID: 3515804
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
    Seys E; Andrini O; Keck M; Mansour-Hendili L; Courand PY; Simian C; Deschenes G; Kwon T; Bertholet-Thomas A; Bobrie G; Borde JS; Bourdat-Michel G; Decramer S; Cailliez M; Krug P; Cozette P; Delbet JD; Dubourg L; Chaveau D; Fila M; Jourde-Chiche N; Knebelmann B; Lavocat MP; Lemoine S; Djeddi D; Llanas B; Louillet F; Merieau E; Mileva M; Mota-Vieira L; Mousson C; Nobili F; Novo R; Roussey-Kesler G; Vrillon I; Walsh SB; Teulon J; Blanchard A; Vargas-Poussou R
    J Am Soc Nephrol; 2017 Aug; 28(8):2540-2552. PubMed ID: 28381550
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.
    García Castaño A; Pérez de Nanclares G; Madariaga L; Aguirre M; Madrid Á; Chocrón S; Nadal I; Navarro M; Lucas E; Fijo J; Espino M; Espitaletta Z; García Nieto V; Barajas de Frutos D; Loza R; Pintos G; Castaño L; ; Ariceta G
    PLoS One; 2017; 12(3):e0173581. PubMed ID: 28288174
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Progress of research on the role of CLCNKB gene in classical Bartter syndrome].
    Zhou J; Wang C; Bao H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):573-577. PubMed ID: 32335890
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bartter syndrome type III with only a synonymous mutation of the
    Xue Y; Wang B; Tang R; Ni H; Chen P; Liu BC; Zhang X
    Clin Nephrol; 2019 Dec; 92(6):325-328. PubMed ID: 31661060
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Genetic basis of Bartter syndrome in Korea.
    Lee BH; Cho HY; Lee H; Han KH; Kang HG; Ha IS; Lee JH; Park YS; Shin JI; Lee DY; Kim SY; Choi Y; Cheong HI
    Nephrol Dial Transplant; 2012 Apr; 27(4):1516-21. PubMed ID: 21865213
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mixed Bartter-Gitelman syndrome: an inbred family with a heterogeneous phenotype expression of a novel variant in the CLCNKB gene.
    Al-Shibli A; Yusuf M; Abounajab I; Willems PJ
    Springerplus; 2014; 3():96. PubMed ID: 24711981
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bartter syndrome type III with glomerular dysplasia and chronic kidney disease: A case report.
    Liu J; Zhang Y; Wu X; Li Y
    Front Pediatr; 2023; 11():1169486. PubMed ID: 37063660
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.