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Year Number of Results
1990 3
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1994 4
1995 4
1996 6
1997 3
1998 7
1999 10
2000 6
2001 5
2002 19
2003 18
2004 14
2005 16
2006 15
2007 15
2008 20
2009 21
2010 20
2011 15
2012 14
2013 15
2014 7
2015 16
2016 10
2017 16
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2024 2

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351 results

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Page 1
Congenital Long QT Syndrome.
Krahn AD, Laksman Z, Sy RW, Postema PG, Ackerman MJ, Wilde AAM, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 May;8(5):687-706. doi: 10.1016/j.jacep.2022.02.017. JACC Clin Electrophysiol. 2022. PMID: 35589186 Free article. Review.
Congenital long QT syndrome (LQTS) encompasses a group of heritable conditions that are associated with cardiac repolarization dysfunction. ...
Congenital long QT syndrome (LQTS) encompasses a group of heritable conditions that are associated with cardiac …
Diagnosis, management and therapeutic strategies for congenital long QT syndrome.
Wilde AAM, Amin AS, Postema PG. Wilde AAM, et al. Heart. 2022 Mar;108(5):332-338. doi: 10.1136/heartjnl-2020-318259. Epub 2021 May 26. Heart. 2022. PMID: 34039680 Free PMC article. Review.
Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation and life-threatening arrhythmias, leading to syncope and sudden death. ...
Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation and life-th …
CONGENITAL LONG QT SYNDROME: A SYSTEMATIC REVIEW.
Galić E, Bešlić P, Kilić P, Planinić Z, Pašalić A, Galić I, Ćubela VV, Pekić P. Galić E, et al. Acta Clin Croat. 2021 Dec;60(4):739-748. doi: 10.20471/acc.2021.60.04.22. Acta Clin Croat. 2021. PMID: 35734489 Free PMC article. Review.
Congenital long QT syndrome (LQTS) is a disorder of myocardial repolarization defined by a prolonged QT interval on electrocardiogram (ECG) that can cause ventricular arrhythmias and lead to sudden cardiac death. ...
Congenital long QT syndrome (LQTS) is a disorder of myocardial repolarization defined by a prolonged QT interval …
The genetics underlying acquired long QT syndrome: impact for genetic screening.
Itoh H, Crotti L, Aiba T, Spazzolini C, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M. Itoh H, et al. Eur Heart J. 2016 May 7;37(18):1456-64. doi: 10.1093/eurheartj/ehv695. Epub 2015 Dec 28. Eur Heart J. 2016. PMID: 26715165 Free PMC article.
Based on control QTc (without triggers), subjects were designated 'true aLQTS' (QTc within normal limits) or 'unmasked cLQTS' (all others) and compared for QTc and genetics with 2379 members of 1010 genotyped congenital long QT syndrome (cLQTS) familie …
Based on control QTc (without triggers), subjects were designated 'true aLQTS' (QTc within normal limits) or 'unmasked cLQTS' (all others) a …
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.
Adler A, Novelli V, Amin AS, Abiusi E, Care M, Nannenberg EA, Feilotter H, Amenta S, Mazza D, Bikker H, Sturm AC, Garcia J, Ackerman MJ, Hershberger RE, Perez MV, Zareba W, Ware JS, Wilde AAM, Gollob MH. Adler A, et al. Circulation. 2020 Feb 11;141(6):418-428. doi: 10.1161/CIRCULATIONAHA.119.043132. Epub 2020 Jan 27. Circulation. 2020. PMID: 31983240 Free PMC article.
Congenital long QT syndrome: a clinician's guide.
Lankaputhra M, Voskoboinik A. Lankaputhra M, et al. Intern Med J. 2021 Dec;51(12):1999-2011. doi: 10.1111/imj.15437. Intern Med J. 2021. PMID: 34151491 Review.
Congenital long QT syndrome (LQTS) is a familial cardiac ion channelopathy first described over 60 years ago. ...
Congenital long QT syndrome (LQTS) is a familial cardiac ion channelopathy first described over 60 years ago. .. …
Management of Congenital Long-QT Syndrome: Commentary From the Experts.
Kaufman ES, Eckhardt LL, Ackerman MJ, Aziz PF, Behr ER, Cerrone M, Chung MK, Cutler MJ, Etheridge SP, Krahn AD, Lubitz SA, Perez MV, Priori SG, Roberts JD, Roden DM, Schulze-Bahr E, Schwartz PJ, Shimizu W, Shoemaker MB, Sy RW, Towbin JA, Viskin S, A M Wilde A, Zareba W. Kaufman ES, et al. Circ Arrhythm Electrophysiol. 2021 Jul;14(7):e009726. doi: 10.1161/CIRCEP.120.009726. Epub 2021 Jul 9. Circ Arrhythm Electrophysiol. 2021. PMID: 34238011 Free PMC article. Review.
Acquired long QT syndrome and phosphoinositide 3-kinase.
Cohen IS, Lin RZ, Ballou LM. Cohen IS, et al. Trends Cardiovasc Med. 2017 Oct;27(7):451-459. doi: 10.1016/j.tcm.2017.05.005. Epub 2017 May 17. Trends Cardiovasc Med. 2017. PMID: 28687226 Free PMC article. Review.
While it is well known that mutation of several different ion channels can cause congenital long QT syndrome, block of I(Kr) is widely thought to be responsible for most cases of drug-induced acquired long QT syndrome (aLQTS). ...
While it is well known that mutation of several different ion channels can cause congenital long QT syndrome, bl …
Congenital long QT syndrome.
Crotti L, Celano G, Dagradi F, Schwartz PJ. Crotti L, et al. Orphanet J Rare Dis. 2008 Jul 7;3:18. doi: 10.1186/1750-1172-3-18. Orphanet J Rare Dis. 2008. PMID: 18606002 Free PMC article. Review.
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias. ...
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT int …
Sports participation in long QT syndrome.
Aziz PF, Saarel EV. Aziz PF, et al. Cardiol Young. 2017 Jan;27(S1):S43-S48. doi: 10.1017/S1047951116002225. Cardiol Young. 2017. PMID: 28084960 Review.
Untreated congenital long QT syndrome may result in potentially lethal ventricular tachycardia. ...
Untreated congenital long QT syndrome may result in potentially lethal ventricular tachycardia. ...
351 results