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Year Number of Results
1990 1
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2001 1
2002 4
2003 1
2004 3
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2007 2
2008 2
2009 4
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2012 5
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2017 3
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83 results

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Page 1
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.
Mutations in KCNH2 (the gene that encodes hERG1) causes LQT2, one of the most common forms of long QT syndrome, a disorder of cardiac repolarization that predisposes affected subjects to ventricular arrhythmia and increases the risk of sudden cardiac death. . …
Mutations in KCNH2 (the gene that encodes hERG1) causes LQT2, one of the most common forms of long QT syndrome, a disor …
Arrhythmias and Their Electrophysiological Mechanisms in Takotsubo Syndrome: A Narrative Review.
Koh Y, Voskoboinik A, Neil C. Koh Y, et al. Heart Lung Circ. 2022 Aug;31(8):1075-1084. doi: 10.1016/j.hlc.2022.03.010. Epub 2022 May 11. Heart Lung Circ. 2022. PMID: 35562239 Review.
BACKGROUND: Takotsubo syndrome (TTS), an acute and usually reversible condition, is associated with both tachy- and bradyarrhythmias. ...CONCLUSIONS: Takotsubo syndrome, though considered primarily a disease of the myocardium, carries multiple arrhythmic manifestati …
BACKGROUND: Takotsubo syndrome (TTS), an acute and usually reversible condition, is associated with both tachy- and bradyarrhythmias. …
Atrial Fibrillation in Inherited Channelopathies.
Al-Azaam B, Darbar D. Al-Azaam B, et al. Card Electrophysiol Clin. 2021 Mar;13(1):155-163. doi: 10.1016/j.ccep.2020.10.004. Epub 2021 Jan 8. Card Electrophysiol Clin. 2021. PMID: 33516393 Free PMC article. Review.
Impact of Dietary Factors on Brugada Syndrome and Long QT Syndrome.
D'Imperio S, Monasky MM, Micaglio E, Negro G, Pappone C. D'Imperio S, et al. Nutrients. 2021 Jul 21;13(8):2482. doi: 10.3390/nu13082482. Nutrients. 2021. PMID: 34444641 Free PMC article. Review.
A healthy regime is fundamental for the prevention of cardiovascular diseases (CVD). In inherited channelopathies, such as Brugada syndrome (BrS) and Long QT syndrome (LQTS), unfortunately, sudden cardiac death could be the first sign for patients affe …
A healthy regime is fundamental for the prevention of cardiovascular diseases (CVD). In inherited channelopathies, such as Brugada syndro …
Triggers for arrhythmogenesis in the Brugada and long QT 3 syndromes.
Peters CH, Abdelsayed M, Ruben PC. Peters CH, et al. Prog Biophys Mol Biol. 2016 Jan;120(1-3):77-88. doi: 10.1016/j.pbiomolbio.2015.12.009. Epub 2015 Dec 20. Prog Biophys Mol Biol. 2016. PMID: 26713557 Review.
Of these genes, 4 alter sodium currents, and the most common known genetic cause remains loss-of-function mutants in the cardiac sodium channel gene SCN5A. Long QT syndrome (LQTs) has a much longer history and is associated with at least 17 genes. ...In this …
Of these genes, 4 alter sodium currents, and the most common known genetic cause remains loss-of-function mutants in the cardiac sodium chan …
Long-term follow-up of implantable cardioverter-defibrillators in Short QT syndrome.
El-Battrawy I, Besler J, Ansari U, Liebe V, Schimpf R, Tülümen E, Rudic B, Lang S, Odening K, Cyganek L, Wolpert C, Zhou X, Borggrefe M, Akin I. El-Battrawy I, et al. Clin Res Cardiol. 2019 Oct;108(10):1140-1146. doi: 10.1007/s00392-019-01449-3. Epub 2019 Mar 16. Clin Res Cardiol. 2019. PMID: 30879093 Review.
BACKGROUND: Short QT syndrome (SQTS) is associated with sudden cardiac death and implantable cardioverter-defibrillator (ICD) implantation is recommended in this rare disease. ...
BACKGROUND: Short QT syndrome (SQTS) is associated with sudden cardiac death and implantable cardioverter-defibrillator (ICD) …
Autoantibody:Autoantigen Competitor Decoys: Application to Cardiac Phenotypes.
Cardozo T, Cardozo L, Boutjdir M. Cardozo T, et al. Front Immunol. 2022 Jan 28;13:812649. doi: 10.3389/fimmu.2022.812649. eCollection 2022. Front Immunol. 2022. PMID: 35154130 Free PMC article. Review.
Recent opportunities relevant to this approach for cardiac phenotypes, specifically Ro-associated long QT syndrome, are discussed....
Recent opportunities relevant to this approach for cardiac phenotypes, specifically Ro-associated long QT syndrome, are …
Mutation-Specific Differences in Kv7.1 (KCNQ1) and Kv11.1 (KCNH2) Channel Dysfunction and Long QT Syndrome Phenotypes.
Kekenes-Huskey PM, Burgess DE, Sun B, Bartos DC, Rozmus ER, Anderson CL, January CT, Eckhardt LL, Delisle BP. Kekenes-Huskey PM, et al. Int J Mol Sci. 2022 Jul 2;23(13):7389. doi: 10.3390/ijms23137389. Int J Mol Sci. 2022. PMID: 35806392 Free PMC article. Review.
Shortly after the standardization of the 12-lead ECG for the diagnosis of heart disease, several families with autosomal recessive (Jervell and Lange-Nielsen Syndrome) and dominant (Romano-Ward Syndrome) forms of long QT syndrome (LQTS) were ide …
Shortly after the standardization of the 12-lead ECG for the diagnosis of heart disease, several families with autosomal recessive (Jervell …
Remote Monitoring of the QT Interval and Emerging Indications for Arrhythmia Prevention.
Castelletti S, Winkel BG, Schwartz PJ. Castelletti S, et al. Card Electrophysiol Clin. 2021 Sep;13(3):523-530. doi: 10.1016/j.ccep.2021.04.010. Epub 2021 Jul 8. Card Electrophysiol Clin. 2021. PMID: 34330378 Review.
QT interval prolongation is a marker of increased risk for life-threatening arrhythmias, and needs to be promptly recognized. ...The possibility of remote monitoring and QTc measurement for up to 2 weeks, continuously providing physicians with real time data, allows life-s …
QT interval prolongation is a marker of increased risk for life-threatening arrhythmias, and needs to be promptly recognized. ...The …
From novel discovery tools and biomarkers to precision medicine-basic cardiovascular science highlights of 2021/22.
Evans PC, Davidson SM, Wojta J, Bäck M, Bollini S, Brittan M, Catapano AL, Chaudhry B, Cluitmans M, Gnecchi M, Guzik TJ, Hoefer I, Madonna R, Monteiro JP, Morawietz H, Osto E, Padró T, Sluimer JC, Tocchetti CG, Van der Heiden K, Vilahur G, Waltenberger J, Weber C. Evans PC, et al. Cardiovasc Res. 2022 Oct 21;118(13):2754-2767. doi: 10.1093/cvr/cvac114. Cardiovasc Res. 2022. PMID: 35899362 Free PMC article. Review.
We also focus on inducible pluripotent stem cell technology which has demonstrated disease causality for several genetic polymorphisms in long-QT syndrome and aortic valve disease, paving the way for personalized medicine approaches. ...
We also focus on inducible pluripotent stem cell technology which has demonstrated disease causality for several genetic polymorphisms in …
83 results