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

Year Number of Results
2004 1
2005 18
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2007 9
2008 13
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2011 6
2012 8
2013 11
2014 9
2015 10
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2017 6
2018 10
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170 results

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Page 1
Inherited cardiac arrhythmias.
Schwartz PJ, Ackerman MJ, Antzelevitch C, Bezzina CR, Borggrefe M, Cuneo BF, Wilde AAM. Schwartz PJ, et al. Nat Rev Dis Primers. 2020 Jul 16;6(1):58. doi: 10.1038/s41572-020-0188-7. Nat Rev Dis Primers. 2020. PMID: 32678103 Free PMC article. Review.
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricular tachycardia and Brugada syndrome. ...
The main inherited cardiac arrhythmias are long QT syndrome, short QT syndrome, catecholaminergic polymorphic ventricul …
Latent Causes of Sudden Cardiac Arrest.
Krahn AD, Tfelt-Hansen J, Tadros R, Steinberg C, Semsarian C, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 Jun;8(6):806-821. doi: 10.1016/j.jacep.2021.12.014. JACC Clin Electrophysiol. 2022. PMID: 35738861 Free article. Review.
Less common and typically less apparent conditions that may not be readily evident include catecholaminergic polymorphic ventricular tachycardia, short QT syndrome and early repolarization syndrome. In cardiac arrest patients whose extensive testing does not …
Less common and typically less apparent conditions that may not be readily evident include catecholaminergic polymorphic ventricular tachyca …
The measurement of the QT interval.
Postema PG, Wilde AA. Postema PG, et al. Curr Cardiol Rev. 2014 Aug;10(3):287-94. doi: 10.2174/1573403x10666140514103612. Curr Cardiol Rev. 2014. PMID: 24827793 Free PMC article. Review.
Diagnosis and management of short QT syndrome.
Bjerregaard P. Bjerregaard P. Heart Rhythm. 2018 Aug;15(8):1261-1267. doi: 10.1016/j.hrthm.2018.02.034. Epub 2018 Mar 2. Heart Rhythm. 2018. PMID: 29501667 Review.
Establishing a definition of short QT syndrome (SQTS), including symptomatology and QT-interval duration, is still a work in progress. ...
Establishing a definition of short QT syndrome (SQTS), including symptomatology and QT-interval duration, is still a wo …
Pharmacology of Cenobamate: Mechanism of Action, Pharmacokinetics, Drug-Drug Interactions and Tolerability.
Roberti R, De Caro C, Iannone LF, Zaccara G, Lattanzi S, Russo E. Roberti R, et al. CNS Drugs. 2021 Jun;35(6):609-618. doi: 10.1007/s40263-021-00819-8. Epub 2021 May 16. CNS Drugs. 2021. PMID: 33993416 Review.
The most relevant safety issues are currently represented by the risk of severe skin reactions (apparently avoidable by a slow titration) and QT shortening (the drug is contraindicated in patients with familial short QT syndrome or taking QT-shortening drugs) …
The most relevant safety issues are currently represented by the risk of severe skin reactions (apparently avoidable by a slow titration) an …
Short QT syndrome review.
Van Houzen NE, Alsheikh-Ali AA, Garlitski AC, Homoud MK, Weinstock J, Link MS, Estes NA 3rd. Van Houzen NE, et al. J Interv Card Electrophysiol. 2008 Oct;23(1):1-5. doi: 10.1007/s10840-008-9201-x. Epub 2008 Feb 26. J Interv Card Electrophysiol. 2008. PMID: 18299973 Review. No abstract available.
Short QT syndrome in pediatrics.
Pereira R, Campuzano O, Sarquella-Brugada G, Cesar S, Iglesias A, Brugada J, Cruz Filho FES, Brugada R. Pereira R, et al. Clin Res Cardiol. 2017 Jun;106(6):393-400. doi: 10.1007/s00392-017-1094-1. Epub 2017 Mar 16. Clin Res Cardiol. 2017. PMID: 28303324 Review.
Short QT syndrome is a malignant cardiac disease characterized by the presence of ventricular tachyarrhythmias leading to syncope and sudden cardiac death. ...In recent years, clinical, genetic and molecular advances in pathophysiological mechanisms related t
Short QT syndrome is a malignant cardiac disease characterized by the presence of ventricular tachyarrhythmias leading
Short QT syndrome: a review.
Patel U, Pavri BB. Patel U, et al. Cardiol Rev. 2009 Nov-Dec;17(6):300-3. doi: 10.1097/CRD.0b013e3181c07592. Cardiol Rev. 2009. PMID: 19829181 Review.
The initial emphasis was directed toward the congenital long QT syndrome and the Brugada syndrome. Recently, the hereditary short QT syndrome has emerged as yet another rare channelopathy. ...The ability of quinidine and disopyramide to prolong the QT interva …
The initial emphasis was directed toward the congenital long QT syndrome and the Brugada syndrome. Recently, the hereditary short
HERG1 channelopathies.
Sanguinetti MC. Sanguinetti MC. Pflugers Arch. 2010 Jul;460(2):265-76. doi: 10.1007/s00424-009-0758-8. Epub 2009 Nov 22. Pflugers Arch. 2010. PMID: 20544339 Free PMC article. Review.
A single gain-of-function mutation has been described that causes short QT syndrome and cardiac arrhythmia. In addition, up-regulation of hERG1 channel expression has been demonstrated in specific tumors and has been associated with skeletal muscle atrophy in …
A single gain-of-function mutation has been described that causes short QT syndrome and cardiac arrhythmia. In addition …
Short QT syndrome: mechanisms, diagnosis and treatment.
Bjerregaard P, Gussak I. Bjerregaard P, et al. Nat Clin Pract Cardiovasc Med. 2005 Feb;2(2):84-7. doi: 10.1038/ncpcardio0097. Nat Clin Pract Cardiovasc Med. 2005. PMID: 16265378 Review.
Short QT syndrome is an inheritable primary electrical disease of the heart that was discovered in 1999. ...Shortening of the effective refractory period combined with increased dispersion of repolarization is the likely substrate for re-entry and life-threat
Short QT syndrome is an inheritable primary electrical disease of the heart that was discovered in 1999. ...Shortening
170 results