BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 30496127)

  • 1. Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B.
    Fan P; Lu CX; Zhang D; Yang KQ; Lu PP; Zhang Y; Meng X; Hao SF; Luo F; Liu YX; Zhang HM; Song L; Cai J; Zhang X; Zhou XL
    Endocr Connect; 2018 Dec; 7(12):1528-1534. PubMed ID: 30496127
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 32(8):752-758. PubMed ID: 30977777
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 82(4):611-4. PubMed ID: 25378078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A frameshift mutation in the
    Lu Y; Liu X; Sun L; Zhang D; Fan P; Yang K; Zhang L; Liu Y; Zhou X
    Mol Med Rep; 2024 Feb; 29(2):. PubMed ID: 38099339
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 33(7):670-675. PubMed ID: 32161960
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 20(1):389. PubMed ID: 31655555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 30(5):291-299. PubMed ID: 34223773
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 40(2):107-111. PubMed ID: 28718682
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel epithelial sodium channel gamma-subunit de novo frameshift mutation leads to Liddle syndrome.
    Wang Y; Zheng Y; Chen J; Wu H; Zheng D; Hui R
    Clin Endocrinol (Oxf); 2007 Nov; 67(5):801-4. PubMed ID: 17634077
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Novel Frame-Shift Mutation in
    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; 9():896564. PubMed ID: 35774371
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 162(1):166-70. PubMed ID: 22809657
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 146(6):647-651. PubMed ID: 35661050
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel
    Yang Y; Wu C; Qu D; Xu X; Chen L; Sun Q; Zhao X
    Blood Press; 2022 Dec; 31(1):139-145. PubMed ID: 35723567
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Liddle Syndrome due to a Novel c.1713 Deletion in the Epithelial Sodium Channel β-Subunit in a Normotensive Adolescent.
    Brower RK; Ghlichloo IA; Shabgahi V; Elsholz D; Menon RK; Vyas AK
    AACE Clin Case Rep; 2021; 7(1):65-68. PubMed ID: 33851023
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 19(3):. PubMed ID: 29534496
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 19(5):610-619. PubMed ID: 38265765
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Liddle syndrome as a rare cause of hypertension - a case report].
    Bielawska-Niekludow J; Rybi-Szumińska A; Wasilewska A
    Pol Merkur Lekarski; 2019 Nov; 47(281):190-192. PubMed ID: 31812974
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and genetic characteristics of the patients with hypertension and hypokalemia carrying a novel
    Chen M; Lv X; Li J; Guo M; Ma S
    Scand J Clin Lab Invest; 2022; 82(7-8):576-580. PubMed ID: 36336351
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.