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 *

353 related articles for article (PubMed ID: 29534496)

  • 1. Liddle Syndrome: Review of the Literature and Description of a New Case.
    Tetti M; Monticone S; Burrello J; Matarazzo P; Veglio F; Pasini B; Jeunemaitre X; Mulatero P
    Int J Mol Sci; 2018 Mar; 19(3):. PubMed ID: 29534496
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report.
    Kozina AA; Trofimova TA; Okuneva EG; Baryshnikova NV; Obuhova VA; Krasnenko AY; Tsukanov KY; Klimchuk OI; Surkova EI; Shatalov PA; Ilinsky VV
    BMC Nephrol; 2019 Oct; 20(1):389. PubMed ID: 31655555
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Liddle Syndrome with a SCNN1A Mutation: A Case Report and Literature Review.
    Tian J; Xiang F; Wang L; Wu X; Shao L; Ma L; Fang C
    Kidney Blood Press Res; 2024; 49(1):831-838. PubMed ID: 39236685
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.
    Yang KQ; Lu CX; Fan P; Zhang Y; Meng X; Dong XQ; Luo F; Liu YX; Zhang HM; Wu HY; Cai J; Zhang X; Zhou XL
    Clin Exp Hypertens; 2018; 40(2):107-111. PubMed ID: 28718682
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A frameshift mutation in the
    Lu Y; Liu X; Sun L; Zhang D; Fan P; Yang K; Zhang L; Liu Y; Zhou X
    Mol Med Rep; 2024 Feb; 29(2):. PubMed ID: 38099339
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel nonsense mutation in the β-subunit of the epithelial sodium channel causing Liddle syndrome.
    Mareš Š; Filipovský J; Vlková K; Pešta M; Černá V; Hrabák J; Mlíková Seidlerová J; Mayer O
    Blood Press; 2021 Oct; 30(5):291-299. PubMed ID: 34223773
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case.
    Yang KQ; Lu CX; Xiao Y; Liu YX; Jiang XJ; Zhang X; Zhou XL
    Clin Endocrinol (Oxf); 2015 Apr; 82(4):611-4. PubMed ID: 25378078
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome.
    Granhøj J; Nøhr TK; Hinrichs GR; Rasmussen M; Svenningsen P
    Clin J Am Soc Nephrol; 2024 May; 19(5):610-619. PubMed ID: 38265765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
    Fan P; Zhao YM; Zhang D; Liao Y; Yang KQ; Tian T; Lou Y; Luo F; Ma WJ; Zhang HM; Song L; Cai J; Liu YX; Zhou XL
    Am J Hypertens; 2019 Jul; 32(8):752-758. PubMed ID: 30977777
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Family with Liddle Syndrome Caused by a Novel Stop-Gain Mutation in the γ Subunit of Epithelial Sodium Channels.
    Wang X; Cao C; Yao Q; Guo L; Li C; Li J
    Nephron; 2022; 146(6):647-651. PubMed ID: 35661050
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In Liddle Syndrome, Epithelial Sodium Channel Is Hyperactive Mainly in the Early Part of the Aldosterone-Sensitive Distal Nephron.
    Nesterov V; Krueger B; Bertog M; Dahlmann A; Palmisano R; Korbmacher C
    Hypertension; 2016 Jun; 67(6):1256-62. PubMed ID: 27170740
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A family with Liddle syndrome caused by a novel missense mutation in the PY motif of the beta-subunit of the epithelial sodium channel.
    Gao L; Wang L; Liu Y; Zhou X; Hui R; Hu A
    J Pediatr; 2013 Jan; 162(1):166-70. PubMed ID: 22809657
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel
    Yang Y; Wu C; Qu D; Xu X; Chen L; Sun Q; Zhao X
    Blood Press; 2022 Dec; 31(1):139-145. PubMed ID: 35723567
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.
    Fan P; Zhang D; Pan XC; Yang KQ; Zhang QY; Lu YT; Zhang Y; Liu XY; Ma WJ; Zhang HM; Song L; Cai J; Liu YX; Zhou XL
    Kidney Blood Press Res; 2020; 45(4):603-611. PubMed ID: 32698182
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The importance of genetic counseling and genetic screening: a case report of a 16-year-old boy with resistant hypertension and severe hypokalemia.
    Kuang ZM; Wang Y; Wang JJ; Liu JH; Zeng R; Zhou Q; Yu ZQ; Jiang L
    J Am Soc Hypertens; 2017 Mar; 11(3):136-139. PubMed ID: 28236585
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Rare Case of Familiar Hypertension Presenting with Hypertensive Encephalopathy in an Elderly Patient: A Diagnostic Dilemma: A Presentation of Liddle's Syndrome due to Novel Mutation in SCNN1G Gene.
    Suman S; Sudhir M; Nitin S; Vikas M; Simran K; Preet SM
    Saudi J Kidney Dis Transpl; 2021; 32(4):1163-1165. PubMed ID: 35229818
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome.
    Polfus LM; Boerwinkle E; Gibbs RA; Metcalf G; Muzny D; Veeraraghavan N; Grove M; Shete S; Wallace S; Milewicz D; Hanchard N; Lupski JR; Hashmi SS; Gupta-Malhotra M
    Cold Spring Harb Mol Case Stud; 2016 Nov; 2(6):a001255. PubMed ID: 27900368
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Liddle syndrome as a rare cause of hypertension - a case report].
    Bielawska-Niekludow J; Rybi-Szumińska A; Wasilewska A
    Pol Merkur Lekarski; 2019 Nov; 47(281):190-192. PubMed ID: 31812974
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Missense Mutation in the Extracellular Domain of
    Salih M; Gautschi I; van Bemmelen MX; Di Benedetto M; Brooks AS; Lugtenberg D; Schild L; Hoorn EJ
    J Am Soc Nephrol; 2017 Nov; 28(11):3291-3299. PubMed ID: 28710092
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Liddle syndrome].
    Mareš Š; Filipovský J
    Vnitr Lek; 2022; 68(E-8):8-11. PubMed ID: 36575060
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.