Results 61 to 70 of about 1,233,631 (221)

Clinical Outcomes After Catheter Ablation in Patients With Structural Heart Disease and Ventricular Fibrillation

Journal of Cardiovascular Electrophysiology, EarlyView.
ABSTRACT Introduction In patients with ischemic cardiomyopathy (ICM), recurrent VF may be treated with catheter ablation by targeting triggering premature ventricular complexes (PVCs) and/or ventricular scar homogenization. Data on optimal ablation strategies in patients with non‐ischemic cardiomyopathy (NICM) remain limited.
Kenji Hashimoto, Samual Turnbull, Saurabh Kumar   +2 more
wiley   +1 more source

Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

, 2020
Brugada syndrome is a rare inherited arrhythmogenic disease leading to ventricular fibrillation and high risk of sudden death. In 1998, this syndrome was linked with a genetic variant with an autosomal dominant pattern of inheritance.
Sarquella Brugada, Geòrgia, Elena Arbelo, Josep Brugada, Georgia Sarquella-Brugada, Cesar, Sergi, Arbelo, Elena, Brugada, Ramon, Ramon Brugada, Campuzano Larrea, Oscar, Brugada Terradellas, Josep, Oscar Campuzano, Sergi Cesar   +11 more
core   +1 more source

Proposed diagnostic criteria for the Brugada syndrome: consensus report

, 2002
What are the proper diagnostic criteria for identifying Brugada syndrome? A definitive answer to this question has been out of reach and is the reason for the establishment of a special task force of Arrhythmia Working Group of the European Society of ...
Brugada P, Brugada R, Corrado D, Towbin J.A. Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology, Hauer RN, Kass RS, Wilde AA, Brugada J, Antzelevitch C, Borggrefe M, Nademanee K, PRIORI, SILVIA GIULIANA   +11 more
core   +1 more source

Whole‐Exome Sequencing Identifies a Rare CSRP3 Variant Associated With Familial Brugada Syndrome in a Lebanese Family

Journal of Cardiovascular Electrophysiology, EarlyView.
ABSTRACT Introduction Brugada syndrome (BrS) is an inherited arrhythmia associated with an increased risk of sudden cardiac death. Although traditionally regarded as a primary cardiac channelopathy, pathogenic variants in SCN5A account for only 20%–30% of clinically diagnosed cases, leaving most patients genetically unresolved.
Zainab Bashir, Ayat Kadhi, Jad Ballout, Bushra Samara, Maurice Khoury, Georges Nemer, Marwan Refaat   +6 more
wiley   +1 more source

Genetics of Brugada syndrome

Journal of Arrhythmia, 2016
AbstractIn 1992, the Brugada syndrome (BrS) was recognized as a disease responsible for sudden cardiac death, characterized by a right bundle‐branch block with ST segment elevation in the leads V1 and V2. This syndrome is highly associated with sudden cardiac death, especially in young males.
Juang, Jyh-Ming Jimmy, Horie, Minoru
openaire   +3 more sources

Therapy for the Brugada Syndrome [PDF]

, 2006
The Brugada syndrome is a congenital syndrome of sudden cardiac death first described as a new clinical entity in 1992. Electrocardiographically characterized by a distinct coved-type ST segment elevation in the right precordial leads, the syndrome is associated with a high risk for sudden cardiac death in young and otherwise healthy adults, and less ...
C, Antzelevitch, J M, Fish
openaire   +2 more sources

Case Report: Lurasidone-Induced Type 2 Brugada Pattern in a Pediatric Patient

Clinical Practice and Cases in Emergency Medicine
Introduction: Brugada syndrome, a cardiac channelopathy, manifests with ventricular arrhythmia. Diagnosis relies on a type 1 Brugada electrocardiogram (ECG) pattern, while type 2 and type 3 patterns may necessitate electrophysiologic testing to uncover ...
Ethan Start, Aldrin Enabore
doaj   +1 more source

Neurocardiac crosstalk in inherited cardiac arrhythmias and cardiomyopathy

The Journal of Physiology, EarlyView.
Abstract figure legend In inherited cardiac arrhythmias and cardiomyopathy, arrhythmias are typically triggered by autonomic nervous system activity. Genetic mutations linked to these conditions cause pro‐arrhythmic alterations in both cardiomyocytes and neurons, with their pathophysiological crosstalk likely amplifying the manifestation of the disease.
Carol Ann Remme, Molly O'Reilly
wiley   +1 more source

The definition of the Brugada syndrome [PDF]

European Heart Journal, 2017
Brugada syndrome (BS) is an inherited disease characterized by a coved-type ST-segment elevation in the right precordial leads and increased risk of sudden cardiac death (SCD), in the absence of structural abnormalities. The cornerstone of BS diagnosis and definition, is its characteristic ECG pattern that can be present spontaneously or unmasked by ...
Sieira, Juan, Brugada, Pedro
openaire   +3 more sources

Brugada syndrome, Brugada phenocopy or none?

, 2017
Brugada syndrome is a form of inherited arrhythmia syndrome characterized by a distinct ST-segment elevation in the right precordial leads. Brugada phenocopies are clinical entities that present with an electrocardiographic pattern identical to Brugada ...
Adrian Baranchuk, Cuneyt Turkoglu, Hasdemir, Can, Kaya, Esra, Baranchuk, Adrian, Can Hasdemir, Umut Kocabas, Kocabas, Umut, Esra Kaya, Turkoglu, Cuneyt   +9 more
core   +1 more source