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The Brugada syndrome revisited

Trends in Cardiovascular Medicine, 2014
The Brugada syndrome is a rare but well-defined cause of sudden cardiac death. The key underlying abnormality is a decrease in net depolarising current due to a genetic defect, though recent evidence also implicates structural abnormalities in some patients.
Meghavi, Mashar   +3 more
openaire   +2 more sources

Brugada Syndrome 2010

Cardiac Electrophysiology Clinics, 2010
The Brugada syndrome is a genetically determined cardiac disorder, presenting with characteristic electrocardiogram features and high risk of sudden cardiac death from polymorphic ventricular tachycardia/ventricular fibrillation in young individuals with a structurally normal heart.
Paola, Berne, Josep, Brugada
openaire   +2 more sources

Controversies in Brugada syndrome

Trends in Cardiovascular Medicine, 2018
The Brugada syndrome is an inherited channelopathy associated with increased risk of ventricular arrhythmias and sudden death, often occurring during sleep or resting conditions. Although this entity has been described more than 20 years ago, it remains one of the most debated among channelopathies, with several open questions on its genetic substrate,
openaire   +2 more sources

Brugada Syndrome or Brugada Mimicry?

2004
The vast majority of patients dying suddenly within 1 h after the onset of their symptoms have cardiac arrest in the setting of structural heart disease. Such events are most frequently due to ventricular tachyarrhythmias, such as rapid ventricular tachycardia (VT) and ventricular fibrillation (VF).
openaire   +1 more source

Illuminating the Path From Genetics to Clinical Outcome in Brugada Syndrome.

European Heart Journal, 2021
Roddy Walsh, Connie R Bezzina
exaly  

Fever and Brugada Syndrome

Pacing and Clinical Electrophysiology, 2002
Charles, Antzelevitch, Ramon, Brugada
openaire   +2 more sources

Recent Progress in Lynch Syndrome and Other Familial Colorectal Cancer Syndromes

Ca-A Cancer Journal for Clinicians, 2018
Patrick Boland   +2 more
exaly  

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