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Journal Abstract Search

190 related items for PubMed ID: 21525970

  • 1. 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; 24(8):930-5. PubMed ID: 21525970
    [Abstract] [Full Text] [Related]

  • 2. Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunit.
    Rossi E, Farnetti E, Debonneville A, Nicoli D, Grasselli C, Regolisti G, Negro A, Perazzoli F, Casali B, Mantero F, Staub O.
    J Hypertens; 2008 May; 26(5):921-7. PubMed ID: 18398334
    [Abstract] [Full Text] [Related]

  • 3. 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; 125(8):1401-4. PubMed ID: 22613642
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  • 4. 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; 15(10):1091-100. PubMed ID: 9350583
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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
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  • 8. Two sporadic cases of Liddle's syndrome caused by De novo ENaC mutations.
    Yamashita Y, Koga M, Takeda Y, Enomoto N, Uchida S, Hashimoto K, Yamano S, Dohi K, Marumo F, Sasaki S.
    Am J Kidney Dis; 2001 Mar 17; 37(3):499-504. PubMed ID: 11228173
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  • 9. 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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  • 10. 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
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  • 11. 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 23; 82(4):1071-4. PubMed ID: 9100575
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  • 12. [Monogenic hypertension].
    Bähr V, Oelkers W, Diederich S.
    Med Klin (Munich); 2003 Apr 15; 98(4):208-17. PubMed ID: 12715144
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  • 13. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome.
    Hansson JH, Nelson-Williams C, Suzuki H, Schild L, Shimkets R, Lu Y, Canessa C, Iwasaki T, Rossier B, Lifton RP.
    Nat Genet; 1995 Sep 15; 11(1):76-82. PubMed ID: 7550319
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  • 14. 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 15; 162(1):166-70. PubMed ID: 22809657
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  • 16. 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
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  • 17. 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
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  • 18. 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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  • 19. Common variants of the beta and gamma subunits of the epithelial sodium channel and their relation to plasma renin and aldosterone levels in essential hypertension.
    Hannila-Handelberg T, Kontula K, Tikkanen I, Tikkanen T, Fyhrquist F, Helin K, Fodstad H, Piippo K, Miettinen HE, Virtamo J, Krusius T, Sarna S, Gautschi I, Schild L, Hiltunen TP.
    BMC Med Genet; 2005 Jan 20; 6():4. PubMed ID: 15661075
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  • 20. 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 20; 22(1):85-9. PubMed ID: 19344079
    [Abstract] [Full Text] [Related]

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