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Journal Abstract Search

199 related items for PubMed ID: 11798604

  • 1. [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; 40(6):390-3. PubMed ID: 11798604
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  • 2. 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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  • 3. 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; 16(8):1131-5. PubMed ID: 9794716
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  • 5. 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; 82(4):1071-4. PubMed ID: 9100575
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  • 10. A family with Liddle's syndrome caused by a new missense mutation in the beta subunit of the epithelial sodium channel.
    Inoue J, Iwaoka T, Tokunaga H, Takamune K, Naomi S, Araki M, Takahama K, Yamaguchi K, Tomita K.
    J Clin Endocrinol Metab; 1998 Jun; 83(6):2210-3. PubMed ID: 9626162
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  • 11. 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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  • 12. Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension.
    Melander O, Orho M, Fagerudd J, Bengtsson K, Groop PH, Mattiasson I, Groop L, Hulthén UL.
    Hypertension; 1998 May 23; 31(5):1118-24. PubMed ID: 9576123
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  • 13. Identification of a single cytosine base insertion mutation at Arg-597 of the beta subunit of the human epithelial sodium channel in a family with Liddle's disease.
    Inoue T, Okauchi Y, Matsuzaki Y, Kuwajima K, Kondo H, Horiuchi N, Nakao K, Iwata M, Yokogoshi Y, Shintani Y, Bando H, Saito S.
    Eur J Endocrinol; 1998 Jun 23; 138(6):691-7. PubMed ID: 9678538
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  • 14. 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
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  • 16. 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 23; 26(5):921-7. PubMed ID: 18398334
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  • 17. Diagnosis of Liddle syndrome by genetic analysis of beta and gamma subunits of epithelial sodium channel--a report of five affected family members.
    Gao PJ, Zhang KX, Zhu DL, He X, Han ZY, Zhan YM, Yang LW.
    J Hypertens; 2001 May 23; 19(5):885-9. PubMed ID: 11393671
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  • 18. 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
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  • 20. Liddle's syndrome caused by a novel mutation in the proline-rich PY motif of the epithelial sodium channel beta-subunit.
    Furuhashi M, Kitamura K, Adachi M, Miyoshi T, Wakida N, Ura N, Shikano Y, Shinshi Y, Sakamoto K, Hayashi M, Satoh N, Nishitani T, Tomita K, Shimamoto K.
    J Clin Endocrinol Metab; 2005 Jan 23; 90(1):340-4. PubMed ID: 15483078
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