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Journal Abstract Search

221 related items for PubMed ID: 29144530

  • 1. Liddle's syndrome in an African male due to a novel frameshift mutation in the beta-subunit of the epithelial sodium channel gene.
    Freercks R, Meldau S, Jones E, Ensor J, Weimers-Willard C, Rayner B.
    Cardiovasc J Afr; 2017 Sep 23; 28(4):e4-e6. PubMed ID: 29144530
    [Abstract] [Full Text] [Related]

  • 2. Liddle's syndrome associated with a point mutation in the extracellular domain of the epithelial sodium channel gamma subunit.
    Hiltunen TP, Hannila-Handelberg T, Petäjäniemi N, Kantola I, Tikkanen I, Virtamo J, Gautschi I, Schild L, Kontula K.
    J Hypertens; 2002 Dec 23; 20(12):2383-90. PubMed ID: 12473862
    [Abstract] [Full Text] [Related]

  • 3. 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 23; 11(3):136-139. PubMed ID: 28236585
    [Abstract] [Full Text] [Related]

  • 4. A novel mutation in the beta-subunit of the epithelial sodium channel gene (SCNN1B) in a Thai family with Liddle's syndrome.
    Sawathiparnich P, Sumboonnanonda A, Weerakulwattana P, Limwongse C.
    J Pediatr Endocrinol Metab; 2009 Jan 23; 22(1):85-9. PubMed ID: 19344079
    [Abstract] [Full Text] [Related]

  • 5. Aldosterone responsiveness of the epithelial sodium channel (ENaC) in colon is increased in a mouse model for Liddle's syndrome.
    Bertog M, Cuffe JE, Pradervand S, Hummler E, Hartner A, Porst M, Hilgers KF, Rossier BC, Korbmacher C.
    J Physiol; 2008 Jan 15; 586(2):459-75. PubMed ID: 18006588
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [A study of mutation(s) of the epithelial sodium channel gene in a Liddle's syndrome family].
    Ma X, Tian Y, Gao Y, Guo X.
    Zhonghua Nei Ke Za Zhi; 2001 Jun 26; 40(6):390-3. PubMed ID: 11798604
    [Abstract] [Full Text] [Related]

  • 8. The R563Q mutation of the epithelial sodium channel beta-subunit is associated with hypertension.
    Jones ES, Owen EP, Davidson JS, Van Der Merwe L, Rayner BL.
    Cardiovasc J Afr; 2011 Jun 26; 22(5):241-4. PubMed ID: 21107496
    [Abstract] [Full Text] [Related]

  • 9. Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome.
    Jeunemaitre X, Bassilana F, Persu A, Dumont C, Champigny G, Lazdunski M, Corvol P, Barbry P.
    J Hypertens; 1997 Oct 26; 15(10):1091-100. PubMed ID: 9350583
    [Abstract] [Full Text] [Related]

  • 10. Genetic analysis of the epithelial sodium channel in Liddle's syndrome.
    Uehara Y, Sasaguri M, Kinoshita A, Tsuji E, Kiyose H, Taniguchi H, Noda K, Ideishi M, Inoue J, Tomita K, Arakawa K.
    J Hypertens; 1998 Aug 26; 16(8):1131-5. PubMed ID: 9794716
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndrome.
    Rossi E, Farnetti E, Nicoli D, Sazzini M, Perazzoli F, Regolisti G, Grasselli C, Santi R, Negro A, Mazzeo V, Mantero F, Luiselli D, Casali B.
    Am J Hypertens; 2011 Aug 17; 24(8):930-5. PubMed ID: 21525970
    [Abstract] [Full Text] [Related]

  • 13. Molecular genetics of Liddle's syndrome.
    Yang KQ, Xiao Y, Tian T, Gao LG, Zhou XL.
    Clin Chim Acta; 2014 Sep 25; 436():202-6. PubMed ID: 24882431
    [Abstract] [Full Text] [Related]

  • 14. 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 Sep 25; 32(4):1163-1165. PubMed ID: 35229818
    [Abstract] [Full Text] [Related]

  • 15. 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 25; 82(4):611-4. PubMed ID: 25378078
    [Abstract] [Full Text] [Related]

  • 16. Liddle's Syndrome: A Case Report.
    Phoojaroenchanachai M, Buranakitjaroen P, Limwongse C.
    J Med Assoc Thai; 2015 Oct 25; 98(10):1035-40. PubMed ID: 26638596
    [Abstract] [Full Text] [Related]

  • 17. Liddle's-like syndrome associated with nephrotic syndrome secondary to membranous nephropathy: the first case report.
    Yamaguchi E, Yoshikawa K, Nakaya I, Kato K, Miyasato Y, Nakagawa T, Kakizoe Y, Mukoyama M, Soma J.
    BMC Nephrol; 2018 May 23; 19(1):122. PubMed ID: 29792170
    [Abstract] [Full Text] [Related]

  • 18. 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 23; 36(3):502-509. PubMed ID: 28915228
    [Abstract] [Full Text] [Related]

  • 19. 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 23; 30(5):291-299. PubMed ID: 34223773
    [Abstract] [Full Text] [Related]

  • 20. A family with liddle's syndrome caused by a mutation in the beta subunit of the epithelial sodium channel.
    Kyuma M, Ura N, Torii T, Takeuchi H, Takizawa H, Kitamura K, Tomita K, Sasaki S, Shimamoto K.
    Clin Exp Hypertens; 2001 Aug 23; 23(6):471-8. PubMed ID: 11478429
    [Abstract] [Full Text] [Related]

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