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1963 2
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Page 1
Brugada Syndrome.
Krahn AD, Behr ER, Hamilton R, Probst V, Laksman Z, Han HC. Krahn AD, et al. JACC Clin Electrophysiol. 2022 Mar;8(3):386-405. doi: 10.1016/j.jacep.2021.12.001. JACC Clin Electrophysiol. 2022. PMID: 35331438 Free article. Review.
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and cardiac arrest, predominantly during sleep. ...Despite the perception of BrS being an inherited arrhythmia syndrome, most cases are not associated with a single
Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and cardiac arrest, predominantl
Present Status of Brugada Syndrome: JACC State-of-the-Art Review.
Brugada J, Campuzano O, Arbelo E, Sarquella-Brugada G, Brugada R. Brugada J, et al. J Am Coll Cardiol. 2018 Aug 28;72(9):1046-1059. doi: 10.1016/j.jacc.2018.06.037. J Am Coll Cardiol. 2018. PMID: 30139433 Free article. Review.
The Brugada syndrome is an inherited disorder associated with risk of ventricular fibrillation and sudden cardiac death in a structurally normal heart. ...
The Brugada syndrome is an inherited disorder associated with risk of ventricular fibrillation and sudden cardiac death in a s …
Brugada Syndrome: anesthetic considerations and management algorithm.
Espinosa Á, Ripollés-Melchor J, Brugada R, Campuzano Ó, Sarquella-Brugada G, Abad-Motos A, Zaballos-García M, Abad-Torrent A, Prieto-Gundin A, Brugada J. Espinosa Á, et al. Minerva Anestesiol. 2019 Feb;85(2):173-188. doi: 10.23736/S0375-9393.18.13170-1. Epub 2018 Oct 30. Minerva Anestesiol. 2019. PMID: 30394071 Free article. Review.
Brugada Syndrome is characterized by arrhythmogenic risk that may be exacerbated by different metabolic and pharmacological factors. ...The risk of arrhythmias is well known to increase in the postoperative period, and this risk is particularly accentuated in patien
Brugada Syndrome is characterized by arrhythmogenic risk that may be exacerbated by different metabolic and pharmacological fa
Brugada syndrome: Diagnosis, risk stratification and management.
Gourraud JB, Barc J, Thollet A, Le Marec H, Probst V. Gourraud JB, et al. Arch Cardiovasc Dis. 2017 Mar;110(3):188-195. doi: 10.1016/j.acvd.2016.09.009. Epub 2017 Jan 27. Arch Cardiovasc Dis. 2017. PMID: 28139454 Free article. Review.
Brugada syndrome is a rare inherited arrhythmia syndrome leading to an increased risk of sudden cardiac death, despite a structurally normal heart. ...As implantable cardiac defibrillators - the main therapy in Brugada syndrome - are associated
Brugada syndrome is a rare inherited arrhythmia syndrome leading to an increased risk of sudden cardiac death, despite
Brugada syndrome: update and future perspectives.
Marsman EMJ, Postema PG, Remme CA. Marsman EMJ, et al. Heart. 2022 May;108(9):668-675. doi: 10.1136/heartjnl-2020-318258. Epub 2021 Oct 14. Heart. 2022. PMID: 34649929 Review.
Brugada syndrome (BrS) is an inherited cardiac disorder, characterised by a typical ECG pattern and an increased risk of arrhythmias and sudden cardiac death (SCD). ...
Brugada syndrome (BrS) is an inherited cardiac disorder, characterised by a typical ECG pattern and an increased risk of arrhy
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.
Inherited arrhythmia syndromes are a common cause of apparently unexplained cardiac arrest or sudden cardiac death. These include long QT syndrome and Brugada syndrome, with a well-recognized phenotype in most patients with sufficiently severe disease to lead …
Inherited arrhythmia syndromes are a common cause of apparently unexplained cardiac arrest or sudden cardiac death. These include long QT …
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.
Gain-of-function mutations in SCN5A lead to more sodium influx into cardiomyocytes through aberrant channel gating and cause long QT syndrome, a primary electrical disease of the heart. Loss-of-function mutations in SCN5A lead to lower expression levels of SCN5A or product …
Gain-of-function mutations in SCN5A lead to more sodium influx into cardiomyocytes through aberrant channel gating and cause long QT synd
Anesthetic management of patients with Brugada syndrome: a case series and literature review.
Kloesel B, Ackerman MJ, Sprung J, Narr BJ, Weingarten TN. Kloesel B, et al. Can J Anaesth. 2011 Sep;58(9):824-36. doi: 10.1007/s12630-011-9546-y. Epub 2011 Jun 23. Can J Anaesth. 2011. PMID: 21698509 Review.
PURPOSE: To review the anesthetic management and perioperative outcomes of patients diagnosed with Brugada syndrome (BrS) who were treated at a single centre and to compare those results with a comprehensive review of the existing literature. ...A literature review …
PURPOSE: To review the anesthetic management and perioperative outcomes of patients diagnosed with Brugada syndrome (BrS) who …
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
850 results