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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. ...The management of LQTS involves conservative measures such as the avoidance of QT-prolonging drugs, pharmacol …
Congenital long QT syndrome (LQTS) encompasses a group of heritable conditions that are associated with cardiac repolar …
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. ...The initial diagnostic evaluation of …
Congenital long QT syndrome (LQTS) is a disorder of myocardial repolarization defined by a prolonged QT interval …
Drug-induced QT Interval Prolongation in the Intensive Care Unit.
Etchegoyen CV, Keller GA, Mrad S, Cheng S, Di Girolamo G. Etchegoyen CV, et al. Curr Clin Pharmacol. 2017;12(4):210-222. doi: 10.2174/1574884713666180223123947. Curr Clin Pharmacol. 2017. PMID: 29473523 Review.
BACKGROUND: The most common acquired cause of Long QT syndrome (LQTS) is drug induced QT interval prolongation. It is an electrophysiological entity, which is characterized by an extended duration of the ventricular repolarization. Reflected as a prolo …
BACKGROUND: The most common acquired cause of Long QT syndrome (LQTS) is drug induced QT interval prolongation. …
CACNA1C-Related Channelopathies.
Herold KG, Hussey JW, Dick IE. Herold KG, et al. Handb Exp Pharmacol. 2023;279:159-181. doi: 10.1007/164_2022_624. Handb Exp Pharmacol. 2023. PMID: 36598608 Free PMC article. Review.
The first mutations identified within CACNA1C were shown to cause a severe, multisystem disorder known as Timothy syndrome (TS), which is characterized by neurodevelopmental deficits, long-QT syndrome, life-threatening cardiac arrhythmias, craniofacial …
The first mutations identified within CACNA1C were shown to cause a severe, multisystem disorder known as Timothy syndrome (TS), whic …
Calmodulin Mutations in Human Disease.
Hussey JW, Limpitikul WB, Dick IE. Hussey JW, et al. Channels (Austin). 2023 Dec;17(1):2165278. doi: 10.1080/19336950.2023.2165278. Channels (Austin). 2023. PMID: 36629534 Free PMC article. Review.
Mutations within any of these three genes may lead to severe cardiac deficits including severe long QT syndrome (LQTS) and/or catecholaminergic polymorphic ventricular tachycardia (CPVT). ...
Mutations within any of these three genes may lead to severe cardiac deficits including severe long QT syndrome (LQTS) …
Repolarization syndromes.
Bhatia A, Sra J, Akhtar M. Bhatia A, et al. Curr Probl Cardiol. 2012 Aug;37(8):317-62. doi: 10.1016/j.cpcardiol.2012.03.004. Curr Probl Cardiol. 2012. PMID: 22749026 Review.
Repolarization syndromes, including early repolarization, Brugada, and short and long QT, have been implicated increasingly as causes of sudden cardiac death (SCD) despite no obvious mechanical cardiac abnormalities. ...Underlying mechanisms for ventricular tachycar …
Repolarization syndromes, including early repolarization, Brugada, and short and long QT, have been implicated increasingly as …
Update on long QT syndrome.
Neira V, Enriquez A, Simpson C, Baranchuk A. Neira V, et al. J Cardiovasc Electrophysiol. 2019 Dec;30(12):3068-3078. doi: 10.1111/jce.14227. Epub 2019 Oct 14. J Cardiovasc Electrophysiol. 2019. PMID: 31596038 Review.
Long QT syndrome (LQTS) is an inherited disorder characterized by a prolonged QT interval in the 12-lead electrocardiogram and increased risk of malignant arrhythmias in patients with a structurally normal heart. ...
Long QT syndrome (LQTS) is an inherited disorder characterized by a prolonged QT interval in the 12-lead …
Genetics of long-QT syndrome.
Nakano Y, Shimizu W. Nakano Y, et al. J Hum Genet. 2016 Jan;61(1):51-5. doi: 10.1038/jhg.2015.74. Epub 2015 Jun 25. J Hum Genet. 2016. PMID: 26108145 Review.
Congenital long QT syndrome (LQTS) is an inherited arrhythmia syndrome characterized by a prolonged QT interval in the 12-lead ECG, torsades de pointes and not negligible prevalence of sudden cardiac death. ...A total of 15 genes have bee …
Congenital long QT syndrome (LQTS) is an inherited arrhythmia syndrome characterized by a prolonged QT in …
Genome Editing and Cardiac Arrhythmias.
Moore OM, Ho KS, Copeland JS, Parthasarathy V, Wehrens XHT. Moore OM, et al. Cells. 2023 May 11;12(10):1363. doi: 10.3390/cells12101363. Cells. 2023. PMID: 37408197 Free PMC article. Review.
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 associated sy …
Congenital long QT syndrome (LQTS) is a familial cardiac ion channelopathy first described over 60 years ago. It is cha …
202 results