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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 …
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.
Meta-analysis of T(peak)-T(end) and T(peak)-T(end)/QT ratio for risk stratification in congenital long QT syndrome.
Tse G, Gong M, Meng L, Wong CW, Georgopoulos S, Bazoukis G, Wong MCS, Letsas KP, Vassiliou VS, Xia Y, Baranchuk AM, Yan GX, Liu T. Tse G, et al. J Electrocardiol. 2018 May-Jun;51(3):396-401. doi: 10.1016/j.jelectrocard.2018.03.001. Epub 2018 Mar 6. J Electrocardiol. 2018. PMID: 29550106
BACKGROUND AND OBJECTIVES: Congenital long QT syndrome (LQTS) predisposes affected individuals to ventricular tachycardia/fibrillation (VF/VF), potentially resulting in sudden cardiac death. ...
BACKGROUND AND OBJECTIVES: Congenital long QT syndrome (LQTS) predisposes affected individuals to ventricular ta …
Effect of female sex on cardiac arrhythmias.
Gowd BM, Thompson PD. Gowd BM, et al. Cardiol Rev. 2012 Nov-Dec;20(6):297-303. doi: 10.1097/CRD.0b013e318259294b. Cardiol Rev. 2012. PMID: 22531673 Review.
Women are generally less prone to ventricular arrhythmias, but they comprise a higher percentage of symptomatic subjects with congenital long QT syndrome and are more often affected by drugs that prolong the QT. ...
Women are generally less prone to ventricular arrhythmias, but they comprise a higher percentage of symptomatic subjects with congenital …
Implantable defibrillators versus medical therapy for cardiac channelopathies.
McNamara DA, Goldberger JJ, Berendsen MA, Huffman MD. McNamara DA, et al. Cochrane Database Syst Rev. 2015 Oct 7;2015(10):CD011168. doi: 10.1002/14651858.CD011168.pub2. Cochrane Database Syst Rev. 2015. PMID: 26445202 Free PMC article. Review.
SELECTION CRITERIA: We included all randomized controlled trials of people aged 18 years and older with ion channelopathies, including congenital long QT syndrome, congenital short QT syndrome, Brugada syndrome, or catecholaminergic polymorphic ventric …
SELECTION CRITERIA: We included all randomized controlled trials of people aged 18 years and older with ion channelopathies, including co …