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Year Number of Results
1977 1
1979 1
1984 3
1985 4
1986 2
1987 2
1988 2
1989 6
1990 9
1991 9
1992 17
1993 26
1994 20
1995 22
1996 30
1997 32
1998 41
1999 65
2000 69
2001 61
2002 87
2003 87
2004 71
2005 114
2006 88
2007 84
2008 84
2009 75
2010 109
2011 66
2012 75
2013 90
2014 78
2015 89
2016 76
2017 68
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2019 56
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2023 52
2024 14

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1,991 results

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Page 1
Long QT Syndrome: A Comprehensive Review of the Literature and Current Evidence.
Shah SR, Park K, Alweis R. Shah SR, et al. Curr Probl Cardiol. 2019 Mar;44(3):92-106. doi: 10.1016/j.cpcardiol.2018.04.002. Epub 2018 May 10. Curr Probl Cardiol. 2019. PMID: 29784533 Review.
Long QT syndrome (LQT) represents a heterogeneous family of cardiac electrophysiologic disorders characterized by QT prolongation and T-wave abnormalities on the electrocardiogram. ...Awareness should be raised regarding possible circumstances that cou …
Long QT syndrome (LQT) represents a heterogeneous family of cardiac electrophysiologic disorders characterized by QT …
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 …
Long QT Syndrome: Genetics and Future Perspective.
Wallace E, Howard L, Liu M, O'Brien T, Ward D, Shen S, Prendiville T. Wallace E, et al. Pediatr Cardiol. 2019 Oct;40(7):1419-1430. doi: 10.1007/s00246-019-02151-x. Epub 2019 Aug 22. Pediatr Cardiol. 2019. PMID: 31440766 Free PMC article. Review.
Long QT syndrome (LQTS) is an inherited primary arrhythmia syndrome that may present with malignant arrhythmia and, rarely, risk of sudden death. ...This predisposition to malignant arrhythmia is from a cardiac ion channelopathy that results in delayed …
Long QT syndrome (LQTS) is an inherited primary arrhythmia syndrome that may present with malignant arrhythmia a …
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 …
Long-QT syndrome: from genetics to management.
Schwartz PJ, Crotti L, Insolia R. Schwartz PJ, et al. Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):868-77. doi: 10.1161/CIRCEP.111.962019. Circ Arrhythm Electrophysiol. 2012. PMID: 22895603 Free PMC article. Review. No abstract available.
Managing drug-induced QT prolongation in clinical practice.
Khatib R, Sabir FRN, Omari C, Pepper C, Tayebjee MH. Khatib R, et al. Postgrad Med J. 2021 Jul;97(1149):452-458. doi: 10.1136/postgradmedj-2020-138661. Epub 2020 Oct 29. Postgrad Med J. 2021. PMID: 33122341 Free PMC article. Review.
As the QT interval varies with a change in heart rate, various formulae can adjust for this, producing a 'corrected QT' (QTc) value. ...To support clinicians, who are likely to prescribe such medicines in their daily practice, we developed a simple algorithm to help …
As the QT interval varies with a change in heart rate, various formulae can adjust for this, producing a 'corrected QT' (QTc) …
Pharmacological treatment of acquired QT prolongation and torsades de pointes.
Thomas SH, Behr ER. Thomas SH, et al. Br J Clin Pharmacol. 2016 Mar;81(3):420-7. doi: 10.1111/bcp.12726. Epub 2015 Oct 26. Br J Clin Pharmacol. 2016. PMID: 26183037 Free PMC article. Review.
Acquired long QT syndromes are mainly caused by cardiac disease, electrolyte abnormalities or exposure to drugs that block rectifying potassium channels, especially IKr. Management of TdP or marked QT prolongation includes removal or correction of precipitant …
Acquired long QT syndromes are mainly caused by cardiac disease, electrolyte abnormalities or exposure to drugs that block rec …
Long-QT syndrome.
Kramer DB, Zimetbaum PJ. Kramer DB, et al. Cardiol Rev. 2011 Sep-Oct;19(5):217-25. doi: 10.1097/CRD.0b013e3182203504. Cardiol Rev. 2011. PMID: 21808164 Review.
Acquired and hereditary long-QT syndromes are important causes of sudden cardiac death. Both categories are characterized by abnormally prolonged cardiac repolarization arising from a complex interaction between genetic and environmental factors. ...In this review, …
Acquired and hereditary long-QT syndromes are important causes of sudden cardiac death. Both categories are characterized by a …
1,991 results