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Items: 1 to 20 of 89

1.

QTc prolongation and family history of sudden death in a patient with desmin cardiomyopathy.

Sung RK, Ursell PC, Rame JE, Bailey H, Caleshu C, Nussbaum RL, Scheinman MM.

Pacing Clin Electrophysiol. 2011 Dec;34(12):e105-8. doi: 10.1111/j.1540-8159.2010.02826.x. Epub 2010 Jul 15.

PMID:
20636320
2.

Investigation of ion channel gene variants in patients with long QT syndrome.

Ernesto C, Cruz FE, Lima FS, Coutinho JL, Silva R, Urményi TP, Carvalho AC, Rondinelli E.

Arq Bras Cardiol. 2011 Mar;96(3):172-8. Epub 2011 Feb 4. English, Portuguese, Spanish.

3.
4.

The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.

Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J.

J Cardiovasc Electrophysiol. 2012 Oct;23(10):1092-8. doi: 10.1111/j.1540-8167.2012.02371.x. Epub 2012 Aug 6.

PMID:
22882672
5.

Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?

Kiehne N, Kauferstein S.

Forensic Sci Int Genet. 2007 Jun;1(2):170-4. doi: 10.1016/j.fsigen.2007.01.009. Epub 2007 Feb 26.

PMID:
19083750
6.

The inherited long QT syndrome: from ion channel to bedside.

Vincent GM, Timothy K, Fox J, Zhang L.

Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Review.

PMID:
10348966
7.

Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.

Trolle C, Mortensen KH, Pedersen LN, Berglund A, Jensen HK, Andersen NH, Gravholt CH.

PLoS One. 2013 Jul 25;8(7):e69614. doi: 10.1371/journal.pone.0069614. Print 2013.

8.

Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.

Barc J, Briec F, Schmitt S, Kyndt F, Le Cunff M, Baron E, Vieyres C, Sacher F, Redon R, Le Caignec C, Le Marec H, Probst V, Schott JJ.

J Am Coll Cardiol. 2011 Jan 4;57(1):40-7. doi: 10.1016/j.jacc.2010.08.621.

9.
10.

Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutation.

Barsheshet A, Moss AJ, McNitt S, Polonsky S, Lopes CM, Zareba W, Robinson JL, Ackerman MJ, Benhorin J, Kaufman ES, Towbin JA, Vincent GM, Qi M, Goldenberg I.

Circ Cardiovasc Genet. 2011 Oct;4(5):491-9. doi: 10.1161/CIRCGENETICS.111.960179. Epub 2011 Aug 10.

11.

LQT3: who is at risk for sudden cardiac death?

Eckardt L.

Heart Rhythm. 2009 Jan;6(1):121-2. doi: 10.1016/j.hrthm.2008.12.004. Epub 2008 Dec 6. No abstract available.

PMID:
19121812
12.

[Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].

Shi RM, Ma AQ, Zhang YM, Yang C, Huang C, Zhou XH, Liu XH.

Zhonghua Er Ke Za Zhi. 2009 Dec;47(12):926-30. Chinese.

PMID:
20193146
13.

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.

Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P; D.E.S.I.R. Study Group.

Eur J Hum Genet. 2005 Nov;13(11):1213-22.

14.

Molecular autopsy for sudden unexplained death? Time to discuss pros and cons.

Mazzanti A, Priori SG.

J Cardiovasc Electrophysiol. 2012 Oct;23(10):1099-102. doi: 10.1111/j.1540-8167.2012.02430.x. Epub 2012 Sep 11. No abstract available.

PMID:
22966897
15.

Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant.

Crotti L, Hu D, Barajas-Martinez H, De Ferrari GM, Oliva A, Insolia R, Pollevick GD, Dagradi F, Guerchicoff A, Greco F, Schwartz PJ, Viskin S, Antzelevitch C.

Heart Rhythm. 2012 Jul;9(7):1104-12. doi: 10.1016/j.hrthm.2012.02.014. Epub 2012 Feb 13.

16.

Genetics of long QT syndrome.

Tester DJ, Ackerman MJ.

Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):29-33. Review.

17.

The long QT syndromes: genetic basis and clinical implications.

Chiang CE, Roden DM.

J Am Coll Cardiol. 2000 Jul;36(1):1-12. Review.

18.

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.

Circ Arrhythm Electrophysiol. 2010 Apr;3(2):120-5. doi: 10.1161/CIRCEP.109.907865. Epub 2010 Jan 9.

19.

25th anniversary of the International Long-QT Syndrome Registry: an ongoing quest to uncover the secrets of long-QT syndrome.

Moss AJ, Schwartz PJ.

Circulation. 2005 Mar 8;111(9):1199-201. Review. No abstract available.

20.

Molecular genetic basis of sudden cardiac death.

Towbin JA.

Pediatr Clin North Am. 2004 Oct;51(5):1229-55. Review.

PMID:
15331282

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