Similar articles for PMID: 18452873

Year	Number of Results
1996	1
1997	1
1998	1
1999	3
2000	3
2001	2
2002	4
2003	4
2004	6
2005	3
2006	5
2007	4
2008	8
2009	5
2010	6
2011	6
2012	10
2013	8
2014	6
2015	5
2016	3
2017	1
2018	5
2019	2
2020	1
2022	1
2023	1
2024	0

1

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome.

Johnson JN, Tester DJ, Perry J, Salisbury BA, Reed CR, Ackerman MJ. Johnson JN, et al. Heart Rhythm. 2008 May;5(5):704-9. doi: 10.1016/j.hrthm.2008.02.007. Epub 2008 Feb 8. Heart Rhythm. 2008. PMID: 18452873 Free PMC article.

2

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.

Tester DJ, Will ML, Haglund CM, Ackerman MJ. Tester DJ, et al. Heart Rhythm. 2005 May;2(5):507-17. doi: 10.1016/j.hrthm.2005.01.020. Heart Rhythm. 2005. PMID: 15840476

3

Atrial Fibrillation in Long QT Syndrome by Genotype.

Platonov PG, McNitt S, Polonsky B, Rosero SZ, Zareba W. Platonov PG, et al. Circ Arrhythm Electrophysiol. 2019 Oct;12(10):e007213. doi: 10.1161/CIRCEP.119.007213. Epub 2019 Oct 15. Circ Arrhythm Electrophysiol. 2019. PMID: 31610692 Free PMC article.

4

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.

Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ. Kapplinger JD, et al. Heart Rhythm. 2009 Sep;6(9):1297-303. doi: 10.1016/j.hrthm.2009.05.021. Epub 2009 Jun 23. Heart Rhythm. 2009. PMID: 19716085 Free PMC article.

5

Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.

Wong JA, Gula LJ, Klein GJ, Yee R, Skanes AC, Krahn AD. Wong JA, et al. Circ Arrhythm Electrophysiol. 2010 Apr;3(2):120-5. doi: 10.1161/CIRCEP.109.907865. Epub 2010 Jan 9. Circ Arrhythm Electrophysiol. 2010. PMID: 20071715 Clinical Trial.

6

Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.

Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, Schwartz PJ, Vincent GM, Priori SG, Benhorin J, Towbin JA, Robinson JL, Andrews ML, Napolitano C, Timothy K, Zhang L, Medina A; International Long QT Syndrome Registry. Zareba W, et al. J Am Coll Cardiol. 2003 Jul 2;42(1):103-9. doi: 10.1016/s0735-1097(03)00554-0. J Am Coll Cardiol. 2003. PMID: 12849668 Free article.

7

A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation.

Benito B, Brugada R, Perich RM, Lizotte E, Cinca J, Mont L, Berruezo A, Tolosana JM, Freixa X, Brugada P, Brugada J. Benito B, et al. Heart Rhythm. 2008 Oct;5(10):1434-40. doi: 10.1016/j.hrthm.2008.07.013. Epub 2008 Jul 19. Heart Rhythm. 2008. PMID: 18929331

8

Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.

Tester DJ, Cronk LB, Carr JL, Schulz V, Salisbury BA, Judson RS, Ackerman MJ. Tester DJ, et al. Heart Rhythm. 2006 Jul;3(7):815-21. doi: 10.1016/j.hrthm.2006.03.016. Epub 2006 Mar 16. Heart Rhythm. 2006. PMID: 16818214

9

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy.

Johnson JN, Hofman N, Haglund CM, Cascino GD, Wilde AA, Ackerman MJ. Johnson JN, et al. Neurology. 2009 Jan 20;72(3):224-31. doi: 10.1212/01.wnl.0000335760.02995.ca. Epub 2008 Nov 26. Neurology. 2009. PMID: 19038855 Free PMC article.

10

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.

Olesen MS, Yuan L, Liang B, Holst AG, Nielsen N, Nielsen JB, Hedley PL, Christiansen M, Olesen SP, Haunsø S, Schmitt N, Jespersen T, Svendsen JH. Olesen MS, et al. Circ Cardiovasc Genet. 2012 Aug 1;5(4):450-9. doi: 10.1161/CIRCGENETICS.111.962597. Epub 2012 Jun 8. Circ Cardiovasc Genet. 2012. PMID: 22685113

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