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Journal Abstract Search

149 related items for PubMed ID: 20376790

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  • 5. Premature Stroke Secondary to Severe Hypertension Results from Liddle Syndrome Caused by a Novel SCNN1B Mutation.
    Fan P, Zhang D, Pan XC, Yang KQ, Zhang QY, Lu YT, Zhang Y, Liu XY, Ma WJ, Zhang HM, Song L, Cai J, Liu YX, Zhou XL.
    Kidney Blood Press Res; 2020; 45(4):603-611. PubMed ID: 32698182
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  • 6. 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. 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 17; 30(5):291-299. PubMed ID: 34223773
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  • 12. 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 17; 162(1):166-70. PubMed ID: 22809657
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  • 13. 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 17; 82(4):611-4. PubMed ID: 25378078
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  • 14. 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
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  • 15. 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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  • 16. 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 Jul 18; 146(6):647-651. PubMed ID: 35661050
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  • 17. 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 Jul 18; 44(5):942-949. PubMed ID: 31437854
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  • 20. 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 18; 16(8):1131-5. PubMed ID: 9794716
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