Results 41 to 50 of about 18,700 (219)
Recent Advances in Short QT Syndrome
Frontiers in Cardiovascular Medicine, 2018 Short QT syndrome is a highly malignant inherited cardiac disease characterized by ventricular tachyarrhythmias leading to syncope and sudden cardiac death. It is responsible of lethal episodes in young people, mainly infants.
Oscar Campuzano +16 more
doaj +1 more source
International Journal of Cardiology, 2005 The Brugada syndrome is an autosomal dominant disease with incomplete penetrance that may cause syncope and sudden cardiac death in young individuals with a normal heart. It is characterized by an electrocardiographic pattern of complete or incomplete right bundle branch block and ST segment elevation in leads V1-V3.
Johnson, Francis, Charles, Antzelevitch
openaire +2 more sources
Current electrocardiographic criteria for diagnosis of Brugada pattern: A consensus report
, 2012 Brugada syndrome is an inherited heart disease without structural abnormalities that is thought to arise as a result of accelerated inactivation of Na channels and predominance of transient outward K current (I-to) to generate a voltage gradient in the ...
Breithardt, Guenter +14 more
core +1 more source
Genetic and Molecular Mechanisms in Brugada Syndrome
, 2023 Brugada syndrome is a rare hereditary arrhythmia disorder characterized by a distinctive electrocardiogram pattern and an elevated risk of ventricular arrhythmias and sudden cardiac death in young adults.
Pedro Brugada +6 more
core +1 more source
Revista Portuguesa de Cardiologia, 2017 The authors report the first catheter ablation of Brugada syndrome in the literature using the Rhythmia™ mapping system. Learning points include: (1) low voltage areas can be documented while mapping in some individuals, suggesting that Brugada syndrome ...
Rui Providência +6 more
doaj +1 more source
Genetic Biomarkers in the Risk Assessment of Sudden Cardiac Events: A Personalized Approach
iNew Medicine, EarlyView.Genetic insights into the risk assessment of sudden cardiac events. ABSTRACT Sudden cardiac events are the leading cause of death worldwide. Conventional risk stratification methods, which largely depend on clinical history, imaging, and electrocardiography, are usually inadequate for identifying high‐risk individuals, especially those without visible ...
Shrikant Verma +5 more
wiley +1 more source
Treatment of Electrical Storm with Amiodarone in Brugada Syndrome- an Unexpected Protective Effect [PDF]
, 2013 We are reporting on a 53 year old man with proven Brugada syndrome and ICD implantation for resuscitation in context of polymorphic VT. After recurrent arrhythmia he was treated with Amiodarone.
Novak, J, Lambiase, PD
core
Simultaneous ST-segment elevation in the right precordial and inferior leads in Brugada syndrome
, 2007 We report the case of a patient with genetically confirmed Brugada syndrome who presented with ST-segment elevation in the right precordial and inferior leads.
Angelo Beltrami +10 more
core +1 more source
Brugada syndrome and p.E61X_RANGRF
, 2014 Background: Brugada syndrome is an inherited cardiac condition transmitted with an autosomal dominant pattern which can lead to sudden cardiac death from malignant ventricular arrhythmias.
Iglesias, Anna +6 more
core +2 more sources
Forensic challenges in a case of suspected filicide, matricide, and post‐mortem dismemberment
Journal of Forensic Sciences, EarlyView.Abstract Familicide represents one of the most complex forms of domestic violence in forensic practice. Among intrafamilial homicides, filicide and matricide pose major medico‐legal and criminological challenges, particularly when autopsy findings are nonspecific or severely altered by post‐mortem changes.
Isabella Caristo +4 more
wiley +1 more source