These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 28396810)

  • 1. Management of Liddle Syndrome in Pregnancy: A Case Report and Literature Review.
    Awadalla M; Patwardhan M; Alsamsam A; Imran N
    Case Rep Obstet Gynecol; 2017; 2017():6279460. PubMed ID: 28396810
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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 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]  

  • 7. [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]  

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

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 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. 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]  

  • 15. 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]  

  • 16. A case report of three children with secondary hypertension caused by Liddle syndrome.
    Teoh Z; Shah S
    Clin Nephrol Case Stud; 2020; 8():37-40. PubMed ID: 32566444
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Rare Case of Familiar Hypertension Presenting with Hypertensive Encephalopathy in an Elderly Patient: A Diagnostic Dilemma: A Presentation of Liddle's Syndrome due to Novel Mutation in SCNN1G Gene.
    Suman S; Sudhir M; Nitin S; Vikas M; Simran K; Preet SM
    Saudi J Kidney Dis Transpl; 2021; 32(4):1163-1165. PubMed ID: 35229818
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Liddle syndrome: A case report.
    Jin Y; Qiu W; Yao J
    Med Clin (Barc); 2021 Jun; ():. PubMed ID: 34147249
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Monogenic form of secondary arterial hypertension].
    Bustos-Merlo A; Rosales-Castillo A; Jaén-Águila F
    Hipertens Riesgo Vasc; 2022; 39(3):135-137. PubMed ID: 35660099
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.