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Journal Abstract Search

278 related items for PubMed ID: 28236585

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

  • 2. 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]

  • 3. 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]

  • 4. 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 25; 36(3):502-509. PubMed ID: 28915228
    [Abstract] [Full Text] [Related]

  • 5. 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
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  • 6. 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
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  • 7. 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]

  • 8. 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 Jul 17; 40(2):107-111. PubMed ID: 28718682
    [Abstract] [Full Text] [Related]

  • 9. 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 17; 22(1):85-9. PubMed ID: 19344079
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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 23; 24(8):930-5. PubMed ID: 21525970
    [Abstract] [Full Text] [Related]

  • 12. Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.
    Wang LP, Gao LG, Zhou XL, Wu HY, Zhang L, Wen D, Li YH, Liu YX, Tian T, Fan XH, Jiang XJ, Zhang HM, Hui RT.
    Chin Med J (Engl); 2012 Apr 23; 125(8):1401-4. PubMed ID: 22613642
    [Abstract] [Full Text] [Related]

  • 13. 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
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  • 18. Liddle's syndrome: prospective genetic screening and suppressed aldosterone secretion in an extended kindred.
    Findling JW, Raff H, Hansson JH, Lifton RP.
    J Clin Endocrinol Metab; 1997 Apr 01; 82(4):1071-4. PubMed ID: 9100575
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  • 19. 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
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