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Journal Abstract Search

144 related items for PubMed ID: 31437854

  • 1. 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; 44(5):942-949. PubMed ID: 31437854
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  • 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
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  • 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
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  • 8. 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 18; 162(1):166-70. PubMed ID: 22809657
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  • 11. 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 Jan 18; 40(2):107-111. PubMed ID: 28718682
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  • 12. 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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  • 14. 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 Mar 11; 146(6):647-651. PubMed ID: 35661050
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  • 16. 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
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  • 17. [Liddle's syndrome caused by a novel mutation of the gamma-subunit of epithelial sodium channel gene SCNN1G in Chinese].
    Shi JY, Chen X, Ren Y, Long Y, Tian HM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr 11; 27(2):132-5. PubMed ID: 20376790
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  • 18. A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension.
    Lu YT, Liu XC, Zhou ZM, Zhang D, Sun L, Zhang Y, Fan P, Zhang L, Liu YX, Luo F, Zhou XL.
    Front Cardiovasc Med; 2022 Apr 11; 9():896564. PubMed ID: 35774371
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  • 19. 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 11; 41(3):1569-75. PubMed ID: 24474657
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  • 20. 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 Mar 11; 49(1):831-838. PubMed ID: 39236685
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