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Year Number of Results
1988 1
1997 1
1998 2
1999 3
2000 4
2001 5
2002 5
2003 5
2004 7
2005 11
2006 6
2007 13
2008 10
2009 12
2010 7
2011 6
2012 11
2013 14
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2016 12
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194 results

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Page 1
Clinical Spectrum of SCN5A Mutations: Long QT Syndrome, Brugada Syndrome, and Cardiomyopathy.
Wilde AAM, Amin AS. Wilde AAM, et al. JACC Clin Electrophysiol. 2018 May;4(5):569-579. doi: 10.1016/j.jacep.2018.03.006. Epub 2018 May 2. JACC Clin Electrophysiol. 2018. PMID: 29798782 Free article. Review.
The importance of Na(v)1.5 for normal cardiac electricity is reflected by various disease entities that can be caused by mutations in SCN5A. Gain-of-function mutations in SCN5A lead to more sodium influx into cardiomyocytes through aberrant channel gating and cause long QT …
The importance of Na(v)1.5 for normal cardiac electricity is reflected by various disease entities that can be caused by mutations in …
Brugada syndrome.
Korlipara H, Korlipara G, Pentyala S. Korlipara H, et al. Acta Cardiol. 2021 Oct;76(8):805-824. doi: 10.1080/00015385.2020.1790823. Epub 2020 Jul 20. Acta Cardiol. 2021. PMID: 32684122 Review.
Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome that causes a heightened risk for ventricular tachyarrhythmias and sudden cardiac death. ...Diagnosis of BrS in patients currently relies on presentation with a type-1 Brugada pattern o …
Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome that causes a heightened risk for ventricular tachya …
Brugada syndrome.
Brugada R, Campuzano O, Sarquella-Brugada G, Brugada J, Brugada P. Brugada R, et al. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):25-8. doi: 10.14797/mdcj-10-1-25. Methodist Debakey Cardiovasc J. 2014. PMID: 24932359 Free PMC article. Review.
Brugada syndrome is a rare cardiac arrhythmia characterized by electrocardiographic right bundle branch block and persistent ST-segment elevation in the right precordial leads. ...This brief review focuses on the recent clinical diagnosis, genetic basis, and advance …
Brugada syndrome is a rare cardiac arrhythmia characterized by electrocardiographic right bundle branch block and persistent S …
Risk factors for QTc-prolongation: systematic review of the evidence.
Vandael E, Vandenberk B, Vandenberghe J, Willems R, Foulon V. Vandael E, et al. Int J Clin Pharm. 2017 Feb;39(1):16-25. doi: 10.1007/s11096-016-0414-2. Epub 2016 Dec 23. Int J Clin Pharm. 2017. PMID: 28012118 Review.
Results Ten observational studies could be included, with a total of 89,532 patients [prospective cohort design: N = 6; multiple regression analyses: N = 5; median STROBE score = 17/22 (range 15-18)]. Very strong evidence was found for hypokalemia, use of diuretics, antiar …
Results Ten observational studies could be included, with a total of 89,532 patients [prospective cohort design: N = 6; multiple regression …
Spotlight on the 2022 ESC guideline management of ventricular arrhythmias and prevention of sudden cardiac death: 10 novel key aspects.
Könemann H, Dagres N, Merino JL, Sticherling C, Zeppenfeld K, Tfelt-Hansen J, Eckardt L. Könemann H, et al. Europace. 2023 May 19;25(5):euad091. doi: 10.1093/europace/euad091. Europace. 2023. PMID: 37102266 Free PMC article. Review.
Regarding sudden cardiac death risk stratification, risk calculators for laminopathies, and long QT syndrome are now considered besides the already established risk calculator for hypertrophic cardiomyopathy. Generally, 'new' risk markers beyond left ventricular ejection f …
Regarding sudden cardiac death risk stratification, risk calculators for laminopathies, and long QT syndrome are now considered besid …
The Genetics of Brugada Syndrome.
Cerrone M, Costa S, Delmar M. Cerrone M, et al. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:255-274. doi: 10.1146/annurev-genom-112921-011200. Epub 2022 May 13. Annu Rev Genomics Hum Genet. 2022. PMID: 35567276 Free article. Review.
Brugada syndrome is a heritable channelopathy characterized by a peculiar electrocardiogram (ECG) pattern and increased risk of cardiac arrhythmias and sudden death. ...Even if an overt structural cardiomyopathy is not typical of Brugada syndrome, fibr …
Brugada syndrome is a heritable channelopathy characterized by a peculiar electrocardiogram (ECG) pattern and increased risk o …
Brugada Syndrome.
Refaat MM, Hotait M, Scheinman M. Refaat MM, et al. Card Electrophysiol Clin. 2016 Mar;8(1):239-45. doi: 10.1016/j.ccep.2015.10.036. Card Electrophysiol Clin. 2016. PMID: 26920201 Review.
Brugada syndrome might stay undetected in patients until surviving cardiac arrest. ...
Brugada syndrome might stay undetected in patients until surviving cardiac arrest. ...
Brugada Syndrome: From Molecular Mechanisms and Genetics to Risk Stratification.
Popa IP, Șerban DN, Mărănducă MA, Șerban IL, Tamba BI, Tudorancea I. Popa IP, et al. Int J Mol Sci. 2023 Feb 7;24(4):3328. doi: 10.3390/ijms24043328. Int J Mol Sci. 2023. PMID: 36834739 Free PMC article. Review.
Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG pattern, correlated with an increased risk of ventricular arrhythmias and sudden cardiac death (SCD) in young adults. ...Except for the SCN5A which encodes the cardiac sodium cha …
Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG pattern, correlated with an increased …
Brugada syndrome.
Mizusawa Y, Wilde AA. Mizusawa Y, et al. Circ Arrhythm Electrophysiol. 2012 Jun 1;5(3):606-16. doi: 10.1161/CIRCEP.111.964577. Circ Arrhythm Electrophysiol. 2012. PMID: 22715240 Review. No abstract available.
The Brugada syndrome.
Escárcega RO, Jiménez-Hernández M, Garcia-Carrasco M, Perez-Alva JC, Brugada J. Escárcega RO, et al. Acta Cardiol. 2009 Dec;64(6):795-801. doi: 10.2143/AC.64.6.2044745. Acta Cardiol. 2009. PMID: 20128157 Review.
The genetic abnormalities that cause Brugada syndrome have been linked to mutations in the ion channel gene SCN5A which encodes for the alpha-subunit of the cardiac sodium channel. A consensus conference report published in 2002 described the diagnostic criteria for …
The genetic abnormalities that cause Brugada syndrome have been linked to mutations in the ion channel gene SCN5A which encode …
194 results