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.
22. [Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age]. Akkerhuis JM; Baars HF; Marcelis CL; Akkerhuis KM; Wilde AA Ned Tijdschr Geneeskd; 2007 Oct; 151(43):2357-64. PubMed ID: 18019210 [TBL] [Abstract][Full Text] [Related]
23. Do patients with long QT syndrome remain at risk for sudden cardiac death after 40 years of age? Postema PG; Wilde AA Nat Clin Pract Cardiovasc Med; 2008 Oct; 5(10):602-3. PubMed ID: 18665134 [TBL] [Abstract][Full Text] [Related]
24. Efficacy of different beta-blockers in the treatment of long QT syndrome. Abu-Zeitone A; Peterson DR; Polonsky B; McNitt S; Moss AJ J Am Coll Cardiol; 2014 Sep; 64(13):1352-8. PubMed ID: 25257637 [TBL] [Abstract][Full Text] [Related]
25. Mutation-specific risk in two genetic forms of type 3 long QT syndrome. Liu JF; Moss AJ; Jons C; Benhorin J; Schwartz PJ; Spazzolini C; Crotti L; Ackerman MJ; McNitt S; Robinson JL; Qi M; Goldenberg I; Zareba W Am J Cardiol; 2010 Jan; 105(2):210-3. PubMed ID: 20102920 [TBL] [Abstract][Full Text] [Related]
32. Clinical aspects of the three major genetic forms of long QT syndrome (LQT1, LQT2, LQT3). Kutyifa V; Daimee UA; McNitt S; Polonsky B; Lowenstein C; Cutter K; Lopes C; Zareba W; Moss AJ Ann Noninvasive Electrocardiol; 2018 May; 23(3):e12537. PubMed ID: 29504689 [TBL] [Abstract][Full Text] [Related]
33. Risk Stratification of Type 2 Long-QT Syndrome Mutation Carriers With Normal QTc Interval: The Value of Sex, T-Wave Morphology, and Mutation Type. Platonov PG; McNitt S; Polonsky B; Rosero SZ; Kutyifa V; Huang A; Moss AJ; Zareba W Circ Arrhythm Electrophysiol; 2018 Jul; 11(7):e005918. PubMed ID: 30012873 [TBL] [Abstract][Full Text] [Related]
34. Clinical and genetic profile of congenital long QT syndrome in Hong Kong: a 20-year experience in paediatrics. Kwok SY; Liu AP; Chan CY; Lun KS; Fung JL; Mak CC; Chung BH; Yung TC Hong Kong Med J; 2018 Dec; 24(6):561-570. PubMed ID: 30530868 [TBL] [Abstract][Full Text] [Related]
35. Syncope in genotype-negative long QT syndrome family members. Olde Nordkamp LR; Ruwald MH; Goldenberg I; Wieling W; McNitt S; Polonsky B; Wilde AA; van Dijk N; Moss AJ Am J Cardiol; 2014 Oct; 114(8):1223-8. PubMed ID: 25173441 [TBL] [Abstract][Full Text] [Related]
37. Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study. Lampert R; Day S; Ainsworth B; Burg M; Marino BS; Salberg L; Tome Esteban MT; Abrams DJ; Aziz PF; Barth C; Behr ER; Bell C; Berul CI; Bos JM; Bradley D; Cannom DS; Cannon BC; Concannon MA; Cerrone M; Czosek RJ; Dubin AM; Dziura J; Erickson CC; Estes NAM; Etheridge SP; Goldenberg I; Gray B; Haglund-Turnquist C; Harmon K; James CA; Johnsrude C; Kannankeril P; Lara A; Law IH; Li F; Link MS; Molossi SM; Olshansky B; Noseworthy PA; Saarel EV; Sanatani S; Shah M; Simone L; Skinner J; Tomaselli GF; Ware JS; Webster G; Zareba W; Zipes DP; Ackerman MJ Circulation; 2024 Aug; 150(7):516-530. PubMed ID: 39051104 [TBL] [Abstract][Full Text] [Related]
38. The importance of the epinephrine provocation test for the hidden type-1 congenital long QT syndrome. Atici A; Asoğlu R; Barman HA; Sahin I Turk Kardiyol Dern Ars; 2020 Jun; 48(4):434-438. PubMed ID: 32519984 [TBL] [Abstract][Full Text] [Related]
39. Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry. Chen CJ; Juang JJ; Lin LY; Liu YB; Ho LT; Yu CC; Huang HC; Lin TT; Liao MC; Chen JJ; Hwang JJ; Chen WJ; Yeh SS; Yang DH; Chiang FT; Lin JL; Lai LP; Horie M; QJM; 2019 May; 112(5):343-350. PubMed ID: 30690642 [TBL] [Abstract][Full Text] [Related]