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128 related items for PubMed ID: 35661050

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 26; 20(1):389. PubMed ID: 31655555
    [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 Oct 26; 40(2):107-111. PubMed ID: 28718682
    [Abstract] [Full Text] [Related]

  • 5. A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review.
    Lu Y, Liu X, Sun L, Zhang D, Fan P, Yang K, Zhang L, Liu Y, Zhou X.
    Mol Med Rep; 2024 Feb 26; 29(2):. PubMed ID: 38099339
    [Abstract] [Full Text] [Related]

  • 6. 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 17; 32(8):752-758. PubMed ID: 30977777
    [Abstract] [Full Text] [Related]

  • 7. Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.
    Fan P, Pan XC, Zhang D, Yang KQ, Zhang Y, Tian T, Luo F, Ma WJ, Liu YX, Wang LP, Zhang HM, Song L, Cai J, Zhou XL.
    Am J Hypertens; 2020 Jul 18; 33(7):670-675. PubMed ID: 32161960
    [Abstract] [Full Text] [Related]

  • 8. 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 18; 82(4):611-4. PubMed ID: 25378078
    [Abstract] [Full Text] [Related]

  • 9. 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 11; 19(3):. PubMed ID: 29534496
    [Abstract] [Full Text] [Related]

  • 10. 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 Mar 11; 45(4):603-611. PubMed ID: 32698182
    [Abstract] [Full Text] [Related]

  • 11. 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 11; 162(1):166-70. PubMed ID: 22809657
    [Abstract] [Full Text] [Related]

  • 12. 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 Jan 11; 49(1):831-838. PubMed ID: 39236685
    [Abstract] [Full Text] [Related]

  • 13. Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel SCNN1G mutation is discovered.
    Yang Y, Wu C, Qu D, Xu X, Chen L, Sun Q, Zhao X.
    Blood Press; 2022 Dec 11; 31(1):139-145. PubMed ID: 35723567
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 19(5):610-619. PubMed ID: 38265765
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 2(6):a001255. PubMed ID: 27900368
    [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 Nov 01; 32(4):1163-1165. PubMed ID: 35229818
    [Abstract] [Full Text] [Related]

  • 17. [Liddle syndrome as a rare cause of hypertension - a case report].
    Bielawska-Niekludow J, Rybi-Szumińska A, Wasilewska A.
    Pol Merkur Lekarski; 2019 Nov 29; 47(281):190-192. PubMed ID: 31812974
    [Abstract] [Full Text] [Related]

  • 18. Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family.
    Fan P, Lu CX, Yang KQ, Lu PP, Hao SF, Luo F, Zhang HM, Song L, Wu HY, Cai J, Zhang X, Zhou XL.
    Kidney Blood Press Res; 2019 Nov 29; 44(5):942-949. PubMed ID: 31437854
    [Abstract] [Full Text] [Related]

  • 19. Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients.
    Liu K, Qin F, Sun X, Zhang Y, Wang J, Wu Y, Ma W, Wang W, Wu X, Qin Y, Zhang H, Zhou X, Wu H, Hui R, Zou Y, Jiang X, Song L.
    J Hypertens; 2018 Mar 29; 36(3):502-509. PubMed ID: 28915228
    [Abstract] [Full Text] [Related]

  • 20. Phenotype-genotype analysis in two Chinese families with Liddle syndrome.
    Gong L, Chen J, Shao L, Song W, Hui R, Wang Y.
    Mol Biol Rep; 2014 Mar 29; 41(3):1569-75. PubMed ID: 24474657
    [Abstract] [Full Text] [Related]

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