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Page 1
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. ...Based on the results of a pro
Congenital long QT syndrome (LQTS) is a disorder of myocardial repolarization defined by a prolonged QT i
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
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. It is characterised by prolonged ventricular repolarisation (long QT on electrocardiography), ventricular arrhythmias and associ
Congenital long QT syndrome (LQTS) is a familial cardiac ion channelopathy first described over 60 years ago. It
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.
While published guidelines are useful in the care of patients with long-QT syndrome, it can be difficult to decide how to apply the guidelines to individual patients, particularly those with intermediate risk. We explored the diversity of opinion among 24 cli …
While published guidelines are useful in the care of patients with long-QT syndrome, it can be difficult to decide how …
Congenital Long QT syndrome and torsade de pointes.
El-Sherif N, Turitto G, Boutjdir M. El-Sherif N, et al. Ann Noninvasive Electrocardiol. 2017 Nov;22(6):e12481. doi: 10.1111/anec.12481. Epub 2017 Jul 2. Ann Noninvasive Electrocardiol. 2017. PMID: 28670758 Free PMC article. Review.
Since its initial description by Jervell and Lange-Nielsen in 1957, the congenital long QT syndrome (LQTS) has been the most investigated cardiac ion channelopathy. ...Congenital as well as acquired alterations in certain cardiac ion channels ca …
Since its initial description by Jervell and Lange-Nielsen in 1957, the congenital long QT syndrome (LQTS) has b …
Precision therapy in congenital long QT syndrome.
Neves R, Bains S, Bos JM, MacIntyre C, Giudicessi JR, Ackerman MJ. Neves R, et al. Trends Cardiovasc Med. 2024 Jan;34(1):39-47. doi: 10.1016/j.tcm.2022.06.006. Epub 2022 Jun 27. Trends Cardiovasc Med. 2024. PMID: 35772688 Review.
Long QT syndrome (LQTS) is a potentially life-threatening, but highly treatable genetic heart disease. ...
Long QT syndrome (LQTS) is a potentially life-threatening, but highly treatable genetic heart disease. ...
Molecular Pathophysiology of Congenital Long QT Syndrome.
Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, Kass RS. Bohnen MS, et al. Physiol Rev. 2017 Jan;97(1):89-134. doi: 10.1152/physrev.00008.2016. Physiol Rev. 2017. PMID: 27807201 Free PMC article. Review.
Here we review the molecular determinants, pathogenesis, and pharmacology of congenital Long QT Syndrome. We examine mechanisms of dysfunction associated with three critical cardiac currents that comprise the majority of congenital Long
Here we review the molecular determinants, pathogenesis, and pharmacology of congenital Long QT Syndrome. We exa …
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. ...However, there are a few exceptions: patients with Timothy
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT
Congenital long QT syndrome: considerations for primary care physicians.
Levine E, Rosero SZ, Budzikowski AS, Moss AJ, Zareba W, Daubert JP. Levine E, et al. Cleve Clin J Med. 2008 Aug;75(8):591-600. doi: 10.3949/ccjm.75.8.591. Cleve Clin J Med. 2008. PMID: 18756841 Free article. Review.
Congenital long QT syndrome is an inherited disorder of cardiac repolarization that predisposes to syncope and to sudden death from polymorphic ventricular tachycardia. ...We can now classify some types of congenital long QT syn
Congenital long QT syndrome is an inherited disorder of cardiac repolarization that predisposes to syncope and t
[Congenital long QT syndrome].
Lupoglazoff JM, Denjoy I, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Arch Pediatr. 2001 May;8(5):525-34. doi: 10.1016/s0929-693x(00)00261-x. Arch Pediatr. 2001. PMID: 11396115 Review. French.
Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome characterized by a lengthening of the QT interval on the surface ECG and a propensity to severe ventricular arrhythmias such as torsades de pointes and ventricular fib
Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome characterized by a lengthening of
1,996 results