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Community detection of long QT syndrome with a clinical registry: an alternative to ECG screening programs?

Earle N, Crawford J, Smith W, Hayes I, Shelling A, Hood M, Stiles M, Maxwell F, Heaven D, Love DR, Skinner JR.

Heart Rhythm. 2013 Feb;10(2):233-8. doi: 10.1016/j.hrthm.2012.10.043. Epub 2012 Nov 1.


Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome.

Earle N, Yeo Han D, Pilbrow A, Crawford J, Smith W, Shelling AN, Cameron V, Love DR, Skinner JR.

Heart Rhythm. 2014 Jan;11(1):76-82. doi: 10.1016/j.hrthm.2013.10.005. Epub 2013 Oct 3.


Common Genotypes of Long QT Syndrome in China and the Role of ECG Prediction.

Gao Y, Liu W, Li C, Qiu X, Qin X, Guo B, Liu X, Li J, Yuan Y, Li X, Liang L, Li L, Hong K, Pu J, Liu J, Wang Q, Zhang L, Hu DY.

Cardiology. 2016;133(2):73-8. doi: 10.1159/000440608. Epub 2015 Oct 24.


Diagnostic accuracy of screening electrocardiograms in long QT syndrome I.

Miller MD, Porter Cb, Ackerman MJ.

Pediatrics. 2001 Jul;108(1):8-12.


Routine ECG screening in infancy and early childhood should not be performed.

Skinner JR, Van Hare GF.

Heart Rhythm. 2014 Dec;11(12):2322-7. doi: 10.1016/j.hrthm.2014.09.046. Epub 2014 Sep 18. Review.


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.


Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.

Kumar S, Peters S, Thompson T, Morgan N, Maccicoca I, Trainer A, Zentner D, Kalman JM, Winship I, Vohra JK.

Heart Rhythm. 2013 Nov;10(11):1653-60. doi: 10.1016/j.hrthm.2013.08.022. Epub 2013 Aug 22.


Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.

Tester DJ, Ackerman MJ.

J Am Coll Cardiol. 2007 Jan 16;49(2):240-6. Epub 2006 Dec 29.


Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.

Stattin EL, Boström IM, Winbo A, Cederquist K, Jonasson J, Jonsson BA, Diamant UB, Jensen SM, Rydberg A, Norberg A.

BMC Cardiovasc Disord. 2012 Oct 25;12:95. doi: 10.1186/1471-2261-12-95.


Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.

Locati EH, Zareba W, Moss AJ, Schwartz PJ, Vincent GM, Lehmann MH, Towbin JA, Priori SG, Napolitano C, Robinson JL, Andrews M, Timothy K, Hall WJ.

Circulation. 1998 Jun 9;97(22):2237-44.


Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome.

Theilade J, Kanters J, Henriksen FL, Gilså-Hansen M, Svendsen JH, Eschen O, Toft E, Reimers JI, Tybjærg-Hansen A, Christiansen M, Jensen HK, Bundgaard H.

Cardiology. 2013;126(2):131-7. doi: 10.1159/000350825. Epub 2013 Aug 21.


Diagnostic value of epinephrine test for genotyping LQT1, LQT2, and LQT3 forms of congenital long QT syndrome.

Shimizu W, Noda T, Takaki H, Nagaya N, Satomi K, Kurita T, Suyama K, Aihara N, Sunagawa K, Echigo S, Miyamoto Y, Yoshimasa Y, Nakamura K, Ohe T, Towbin JA, Priori SG, Kamakura S.

Heart Rhythm. 2004 Sep;1(3):276-83.


Long QT syndrome in children.

Zareba W, Moss AJ.

J Electrocardiol. 2001;34 Suppl:167-71.


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.

Heart Rhythm. 2005 May;2(5):507-17.


Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals.

Goldenberg I, Horr S, Moss AJ, Lopes CM, Barsheshet A, McNitt S, Zareba W, Andrews ML, Robinson JL, Locati EH, Ackerman MJ, Benhorin J, Kaufman ES, Napolitano C, Platonov PG, Priori SG, Qi M, Schwartz PJ, Shimizu W, Towbin JA, Vincent GM, Wilde AA, Zhang L.

J Am Coll Cardiol. 2011 Jan 4;57(1):51-9. doi: 10.1016/j.jacc.2010.07.038.


Long QT and Brugada syndrome gene mutations in New Zealand.

Chung SK, MacCormick JM, McCulley CH, Crawford J, Eddy CA, Mitchell EA, Shelling AN, French JK, Skinner JR, Rees MI.

Heart Rhythm. 2007 Oct;4(10):1306-14. Epub 2007 Jul 14.


Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.

Horigome H, Nagashima M, Sumitomo N, Yoshinaga M, Ushinohama H, Iwamoto M, Shiono J, Ichihashi K, Hasegawa S, Yoshikawa T, Matsunaga T, Goto H, Waki K, Arima M, Takasugi H, Tanaka Y, Tauchi N, Ikoma M, Inamura N, Takahashi H, Shimizu W, Horie M.

Circ Arrhythm Electrophysiol. 2010 Feb;3(1):10-7. doi: 10.1161/CIRCEP.109.882159. Epub 2009 Dec 8. Erratum in: Circ Arrhythm Electrophysiol. 2012 Dec;5(6):e120-2.


Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes.

Zhang L, Timothy KW, Vincent GM, Lehmann MH, Fox J, Giuli LC, Shen J, Splawski I, Priori SG, Compton SJ, Yanowitz F, Benhorin J, Moss AJ, Schwartz PJ, Robinson JL, Wang Q, Zareba W, Keating MT, Towbin JA, Napolitano C, Medina A.

Circulation. 2000 Dec 5;102(23):2849-55.


[A novel KCNQ1 mutation in Chinese with congenital long QT syndrome].

Liang L, Du ZD, Cai LL, Wu JX, Zheng T, Qi TX.

Zhonghua Er Ke Za Zhi. 2003 Oct;41(10):724-7. Chinese.


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