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25. 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]
26. Identification of a single cytosine base insertion mutation at Arg-597 of the beta subunit of the human epithelial sodium channel in a family with Liddle's disease. Inoue T; Okauchi Y; Matsuzaki Y; Kuwajima K; Kondo H; Horiuchi N; Nakao K; Iwata M; Yokogoshi Y; Shintani Y; Bando H; Saito S Eur J Endocrinol; 1998 Jun; 138(6):691-7. PubMed ID: 9678538 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system. Schild L; Canessa CM; Shimkets RA; Gautschi I; Lifton RP; Rossier BC Proc Natl Acad Sci U S A; 1995 Jun; 92(12):5699-703. PubMed ID: 7777572 [TBL] [Abstract][Full Text] [Related]
30. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. Shimkets RA; Warnock DG; Bositis CM; Nelson-Williams C; Hansson JH; Schambelan M; Gill JR; Ulick S; Milora RV; Findling JW Cell; 1994 Nov; 79(3):407-14. PubMed ID: 7954808 [TBL] [Abstract][Full Text] [Related]
32. Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel. Snyder PM; Price MP; McDonald FJ; Adams CM; Volk KA; Zeiher BG; Stokes JB; Welsh MJ Cell; 1995 Dec; 83(6):969-78. PubMed ID: 8521520 [TBL] [Abstract][Full Text] [Related]
33. The ENaC channel as the primary determinant of two human diseases: Liddle syndrome and pseudohypoaldosteronism. Schild L Nephrologie; 1996; 17(7):395-400. PubMed ID: 8987044 [TBL] [Abstract][Full Text] [Related]
34. 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; 28(4):e4-e6. PubMed ID: 29144530 [TBL] [Abstract][Full Text] [Related]
35. In Liddle Syndrome, Epithelial Sodium Channel Is Hyperactive Mainly in the Early Part of the Aldosterone-Sensitive Distal Nephron. Nesterov V; Krueger B; Bertog M; Dahlmann A; Palmisano R; Korbmacher C Hypertension; 2016 Jun; 67(6):1256-62. PubMed ID: 27170740 [TBL] [Abstract][Full Text] [Related]
36. Liddle syndrome caused by P616R mutation of the epithelial sodium channel beta subunit. Ciechanowicz A; Dolezel Z; Placha G; Starha J; Góra J; Gaciong Z; Brodkiewicz A; Adler G Pediatr Nephrol; 2005 Jun; 20(6):837-8. PubMed ID: 15856328 [No Abstract] [Full Text] [Related]
37. 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]
38. Cell surface expression of the epithelial Na channel and a mutant causing Liddle syndrome: a quantitative approach. Firsov D; Schild L; Gautschi I; Mérillat AM; Schneeberger E; Rossier BC Proc Natl Acad Sci U S A; 1996 Dec; 93(26):15370-5. PubMed ID: 8986818 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]