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 *

213 related articles for article (PubMed ID: 35668994)

  • 1. The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing.
    Stevenson M; Pagnamenta AT; Mack HG; Savige J; Giacopuzzi E; Lines KE; Taylor JC; Thakker RV
    J Endocr Soc; 2022 Jul; 6(7):bvac079. PubMed ID: 35668994
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

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

  • 4. 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]  

  • 5. [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]  

  • 6. Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathy.
    Nozu K; Yamamura T; Horinouchi T; Nagano C; Sakakibara N; Ishikura K; Hamada R; Morisada N; Iijima K
    Pediatr Int; 2020 Apr; 62(4):428-437. PubMed ID: 31830341
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
    Brochard K; Boyer O; Blanchard A; Loirat C; Niaudet P; Macher MA; Deschenes G; Bensman A; Decramer S; Cochat P; Morin D; Broux F; Caillez M; Guyot C; Novo R; Jeunemaître X; Vargas-Poussou R
    Nephrol Dial Transplant; 2009 May; 24(5):1455-64. PubMed ID: 19096086
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.
    Zelikovic I; Szargel R; Hawash A; Labay V; Hatib I; Cohen N; Nakhoul F
    Kidney Int; 2003 Jan; 63(1):24-32. PubMed ID: 12472765
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Gitelman syndrome.
    Knoers NV; Levtchenko EN
    Orphanet J Rare Dis; 2008 Jul; 3():22. PubMed ID: 18667063
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.
    Jeck N; Konrad M; Peters M; Weber S; Bonzel KE; Seyberth HW
    Pediatr Res; 2000 Dec; 48(6):754-8. PubMed ID: 11102542
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis.
    Najafi M; Kordi-Tamandani DM; Behjati F; Sadeghi-Bojd S; Bakey Z; Karimiani EG; Schüle I; Azarfar A; Schmidts M
    Orphanet J Rare Dis; 2019 Feb; 14(1):41. PubMed ID: 30760291
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The utility of next generation sequencing in the correct diagnosis of congenital hypochloremic hypokalemic metabolic alkalosis.
    Ben-David Y; Halevy R; Sakran W; Zehavi Y; Spiegel R
    Eur J Med Genet; 2019 Oct; 62(10):103728. PubMed ID: 31325522
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.