Results 61 to 70 of about 2,202,317 (252)

In silico modelling of multi‐electrode arrays for enhancing cardiac drug testing on hiPSC‐CM heterogeneous tissues

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend Schematic overview of the experimental and computational framework for investigating hiPSC‐CM electrophysiology with MEA systems. The MEA‐based model integrates experimental data with phenotype‐specific ionic models and tissue‐level heterogeneity.
Sofia Botti   +2 more
wiley   +1 more source

Brugada syndrome in the elderly [PDF]

open access: yesEuropean Heart Journal, 2012
We report the case of a 87-year-old woman, without history of significant cardiovascular diseases, referred to our emergency department because of sudden syncope. Just after being admitted, the patient experienced another sudden syncopal event and a paroxysmal complete atrioventricular (AV) block with narrow QRS complexes ( Panel A …
Conte, G.   +3 more
openaire   +4 more sources

Return‐to‐play in athletes with transvenous and subcutaneous implantable cardiac defibrillator: A meta‐analysis

open access: yesJournal of Arrhythmia, Volume 41, Issue 4, August 2025.
This meta‐analysis of six cohort studies (n = 1,183) found that athletes with transvenous or subcutaneous ICDs had 13% appropriate and 4% inappropriate shock rates, with no serious adverse events. Findings support individualized return‐to‐play decisions, considering arrhythmia type, ICD programming, and psychological support.
Rifqi Rizkani Eri   +5 more
wiley   +1 more source

Genetics of Brugada syndrome [PDF]

open access: yesJournal of Human Genetics, 2015
The Brugada syndrome is characterized by unique 'coved-type' ST-segment elevation in the right precordial leads of electrocardiogram and ventricular fibrillation, and is responsible for 4 to 12% of sudden cardiac death in the general population. The frequency is higher in Southeast Asia including Japan compared with Western countries.
Tohru Minamino, Hiroshi Watanabe
openaire   +2 more sources

Comparison of Two High‐Power Ablation Strategies for Typical Atrial Flutter: Acute and Long‐Term Outcome

open access: yesAnnals of Noninvasive Electrocardiology, Volume 30, Issue 4, July 2025.
ABSTRACT Background Ablation of the cavo‐tricuspid isthmus (CTI) is the standard treatment for typical atrial flutter. High‐power strategies have been described to improve lesion efficacy and durability. Objective To compare the acute success, safety, and long‐term outcomes of two strategies of high‐power CTI ablation using 8‐mm gold‐tip nonirrigated ...
Wael Zaher   +3 more
wiley   +1 more source

Brugada syndrome in a 4-year-old child with Lemierre syndrome—A case report

open access: yesJournal of the Saudi Heart Association, 2018
Brugada syndrome is a rare arrhythmogenic disease with characteristic electrocardiogram (ECG) findings. Fever represents an important triggering factor.
Sami Alanazi   +3 more
doaj  

Alcohol-induced Ventricular Fibrillation in Brugada Syndrome

open access: yesJournal of Arrhythmia, 2009
A 37-year-old man lost consciousness suddenly due to ventricular fibrillation (VF). After cardioversion, twelve-lead ECG showed a pattern characteristic of type 1 Brugada. An implantable cardioverter defibrillator (ICD) was implanted for Brugada syndrome.
Takekuni Hayashi, MD   +11 more
doaj   +1 more source

Fever Unmasked Brugada Syndrome in Pediatric Patient: A Case Report

open access: yesClinical Practice and Cases in Emergency Medicine, 2020
Introduction: Brugada syndrome is an arrhythmogenic disorder that is a known cause of sudden cardiac death. It is characterized by a pattern of ST segment elevation in the precordial leads on an electrocardiogram (EKG) due to a sodium channelopathy. Case
Orhay Mirzapolos   +2 more
doaj   +1 more source

Brugada syndrome, Brugada phenocopy or none? [PDF]

open access: yesAnnals of Noninvasive Electrocardiology, 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 syndrome and may obey to various clinical conditions. We present a case of a suicidal attempt using a
Umut Kocabas   +4 more
openaire   +3 more sources

Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

open access: yesCardiology Research and Practice, 2022
Background. Brugada syndrome is a hereditary cardiac disease associated with mutations in ion channel genes. The clinical features include ventricular fibrillation, syncope, and sudden cardiac death.
Yao-Bin Zhu   +9 more
doaj   +1 more source

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