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149 related items for PubMed ID: 20376790
21. Mutation analysis of SCNN1B in a family with Liddle's syndrome. Wang W, Zhou W, Jiang L, Cui B, Ye L, Su T, Wang J, Li X, Ning G. Endocrine; 2006 Jun; 29(3):385-90. PubMed ID: 16943574 [Abstract] [Full Text] [Related]
22. Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension. Melander O, Orho M, Fagerudd J, Bengtsson K, Groop PH, Mattiasson I, Groop L, Hulthén UL. Hypertension; 1998 May; 31(5):1118-24. PubMed ID: 9576123 [Abstract] [Full Text] [Related]
23. 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 [Abstract] [Full Text] [Related]
28. Liddle's syndrome in an African male due to a novel frameshift mutation in the beta-subunit of the epithelial sodium channel gene. Freercks R, Meldau S, Jones E, Ensor J, Weimers-Willard C, Rayner B. Cardiovasc J Afr; 2017 Sep 23; 28(4):e4-e6. PubMed ID: 29144530 [Abstract] [Full Text] [Related]
37. 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 04; 19(5):885-9. PubMed ID: 11393671 [Abstract] [Full Text] [Related]
38. Vasopressin-stimulated CFTR Cl- currents are increased in the renal collecting duct cells of a mouse model of Liddle's syndrome. Chang CT, Bens M, Hummler E, Boulkroun S, Schild L, Teulon J, Rossier BC, Vandewalle A. J Physiol; 2005 Jan 01; 562(Pt 1):271-84. PubMed ID: 15513933 [Abstract] [Full Text] [Related]
39. 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 [Abstract] [Full Text] [Related]