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 *

170 related articles for article (PubMed ID: 30496127)

  • 21. Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.
    Wang LP; Gao LG; Zhou XL; Wu HY; Zhang L; Wen D; Li YH; Liu YX; Tian T; Fan XH; Jiang XJ; Zhang HM; Hui RT
    Chin Med J (Engl); 2012 Apr; 125(8):1401-4. PubMed ID: 22613642
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A frameshift mutation of beta subunit of epithelial sodium channel in a case of isolated Liddle syndrome.
    Nakano Y; Ishida T; Ozono R; Matsuura H; Yamamoto Y; Kambe M; Chayama K; Oshima T
    J Hypertens; 2002 Dec; 20(12):2379-82. PubMed ID: 12473861
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Use of constant denaturant capillary electrophoresis of pooled blood samples to identify single-nucleotide polymorphisms in the genes (Scnn1a and Scnn1b) encoding the alpha and beta subunits of the epithelial sodium channel.
    Xue MZ; Bonny O; Morgenthaler S; Bochud M; Mooser V; Thilly WG; Schild L; Leong-Morgenthaler PM
    Clin Chem; 2002 May; 48(5):718-28. PubMed ID: 11978598
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Liddle's syndrome associated with a point mutation in the extracellular domain of the epithelial sodium channel gamma subunit.
    Hiltunen TP; Hannila-Handelberg T; Petäjäniemi N; Kantola I; Tikkanen I; Virtamo J; Gautschi I; Schild L; Kontula K
    J Hypertens; 2002 Dec; 20(12):2383-90. PubMed ID: 12473862
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel mutation in the beta-subunit of the epithelial sodium channel gene (SCNN1B) in a Thai family with Liddle's syndrome.
    Sawathiparnich P; Sumboonnanonda A; Weerakulwattana P; Limwongse C
    J Pediatr Endocrinol Metab; 2009 Jan; 22(1):85-9. PubMed ID: 19344079
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A case report of a young boy with low renin and high aldosterone levels induced by Liddle syndrome who was previously misdiagnosed with primary aldosteronism.
    Jin Y; Qiu W; Yao J
    J Pediatr Endocrinol Metab; 2023 Feb; 36(2):212-215. PubMed ID: 36473093
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome.
    Polfus LM; Boerwinkle E; Gibbs RA; Metcalf G; Muzny D; Veeraraghavan N; Grove M; Shete S; Wallace S; Milewicz D; Hanchard N; Lupski JR; Hashmi SS; Gupta-Malhotra M
    Cold Spring Harb Mol Case Stud; 2016 Nov; 2(6):a001255. PubMed ID: 27900368
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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; 41(3):1569-75. PubMed ID: 24474657
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The diagnosis of Liddle syndrome by identification of a mutation in the beta subunit of the epithelial sodium channel.
    Jackson SN; Williams B; Houtman P; Trembath RC
    J Med Genet; 1998 Jun; 35(6):510-2. PubMed ID: 9643296
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

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

  • 32. A family with Liddle's syndrome caused by a new c.1721 deletion mutation in the epithelial sodium channel β-subunit.
    Ding X; Jia N; Zhao C; Zhong Y; Dai D; Zhao Y; Xu C; Cai J; Wang Q; He Q
    Exp Ther Med; 2019 Apr; 17(4):2777-2784. PubMed ID: 30930974
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Liddle's Syndrome: A Case Report.
    Phoojaroenchanachai M; Buranakitjaroen P; Limwongse C
    J Med Assoc Thai; 2015 Oct; 98(10):1035-40. PubMed ID: 26638596
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The importance of genetic counseling and genetic screening: a case report of a 16-year-old boy with resistant hypertension and severe hypokalemia.
    Kuang ZM; Wang Y; Wang JJ; Liu JH; Zeng R; Zhou Q; Yu ZQ; Jiang L
    J Am Soc Hypertens; 2017 Mar; 11(3):136-139. PubMed ID: 28236585
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese Population.
    Wang LP; Yang KQ; Jiang XJ; Wu HY; Zhang HM; Zou YB; Song L; Bian J; Hui RT; Liu YX; Zhou XL
    J Clin Hypertens (Greenwich); 2015 Nov; 17(11):902-7. PubMed ID: 26075967
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A Missense Mutation in the Extracellular Domain of
    Salih M; Gautschi I; van Bemmelen MX; Di Benedetto M; Brooks AS; Lugtenberg D; Schild L; Hoorn EJ
    J Am Soc Nephrol; 2017 Nov; 28(11):3291-3299. PubMed ID: 28710092
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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; 19(5):885-9. PubMed ID: 11393671
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 26(5):921-7. PubMed ID: 18398334
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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; 24(8):930-5. PubMed ID: 21525970
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.