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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 3
1985 1
1987 1
1989 1
1990 3
1991 2
1992 3
1993 10
1994 3
1995 4
1996 10
1997 12
1998 10
1999 17
2000 25
2001 12
2002 30
2003 20
2004 15
2005 24
2006 20
2007 15
2008 20
2009 19
2010 17
2011 8
2012 16
2013 24
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2015 16
2016 16
2017 12
2018 14
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2020 12
2021 9
2022 9
2023 7
2024 2

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441 results

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Page 1
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 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
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, ph
Congenital long QT syndrome (LQTS) encompasses a group of heritable conditions that are associated with cardiac
Fetal Arrhythmia Diagnosis and Pharmacologic Management.
Strasburger JF, Eckstein G, Butler M, Noffke P, Wacker-Gussmann A. Strasburger JF, et al. J Clin Pharmacol. 2022 Sep;62 Suppl 1(Suppl 1):S53-S66. doi: 10.1002/jcph.2129. J Clin Pharmacol. 2022. PMID: 36106782 Free PMC article. Review.
Additionally, transient or hidden arrhythmias such as bundle branch block, QT prolongation, and torsades de pointes, which can lead to cardiomyopathy and sudden unexplained death in the fetus, may also need pharmacologic treatment. ...
Additionally, transient or hidden arrhythmias such as bundle branch block, QT prolongation, and torsades de pointes, which can lead t …
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 …
Muscle channelopathies.
Vivekanandam V, Jayaseelan D, Hanna MG. Vivekanandam V, et al. Handb Clin Neurol. 2023;195:521-532. doi: 10.1016/B978-0-323-98818-6.00006-6. Handb Clin Neurol. 2023. PMID: 37562884 Review.
As genetic testing expands, so have the spectrum of phenotypes seen including pediatric presentations and congenital myopathies. Management of these conditions requires a multidisciplinary approach with extra support needed when patients require anesthetics or when pregnan …
As genetic testing expands, so have the spectrum of phenotypes seen including pediatric presentations and congenital myopathies. Mana …
Fetal dysrhythmias.
Carvalho JS. Carvalho JS. Best Pract Res Clin Obstet Gynaecol. 2019 Jul;58:28-41. doi: 10.1016/j.bpobgyn.2019.01.002. Epub 2019 Jan 9. Best Pract Res Clin Obstet Gynaecol. 2019. PMID: 30738635 Review.
Sinus bradycardia (rate <3rd centile) may be a prenatal marker for long-QT syndrome....
Sinus bradycardia (rate <3rd centile) may be a prenatal marker for long-QT syndrome....
Vandetanib.
Al-Ghusn AI, Bakheit AH, Attwa MW, AlRabiah H. Al-Ghusn AI, et al. Profiles Drug Subst Excip Relat Methodol. 2023;48:109-134. doi: 10.1016/bs.podrm.2022.11.004. Epub 2023 Feb 2. Profiles Drug Subst Excip Relat Methodol. 2023. PMID: 37061272 Review.
Because Vandetanib can make the Q-T interval last longer, it shouldn't be given to people with serious heart problems like congenital long QT syndrome or heart failure that hasn't been fixed yet. ...
Because Vandetanib can make the Q-T interval last longer, it shouldn't be given to people with serious heart problems like congenital
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
Genetic and clinical advances in congenital long QT syndrome.
Mizusawa Y, Horie M, Wilde AA. Mizusawa Y, et al. Circ J. 2014;78(12):2827-33. doi: 10.1253/circj.cj-14-0905. Epub 2014 Oct 1. Circ J. 2014. PMID: 25274057 Free article. Review.
Congenital long QT syndrome (LQTS) is an inherited arrhythmia syndrome characterized by a prolonged QT interval on the 12-lead ECG, torsades de pointes and a higher chance of sudden cardiac death. LQTS segregates in a Mendelian fashion, w
Congenital long QT syndrome (LQTS) is an inherited arrhythmia syndrome characterized by a prolonged QT
441 results