Results 141 to 150 of about 9,222 (174)
Some of the next articles are maybe not open access.
Current Sports Medicine Reports, 2005
Brugada syndrome is a recognized cause of sudden cardiac death worldwide. An inherited ion channel abnormality produces abnormal repolarization leading to characteristic ST-segment elevation in precordial leads V1 to V3 and a pseudo right bundle branch block on electrocardiogram.
Erin B, Drifmeyer, Kenneth B, Batts
openaire +2 more sources
Brugada syndrome is a recognized cause of sudden cardiac death worldwide. An inherited ion channel abnormality produces abnormal repolarization leading to characteristic ST-segment elevation in precordial leads V1 to V3 and a pseudo right bundle branch block on electrocardiogram.
Erin B, Drifmeyer, Kenneth B, Batts
openaire +2 more sources
The American Journal of Emergency Medicine, 2003
Brugada syndrome describes the syndrome of sudden cardiac death in the setting of the following electrocardiographic findings: right bundle branch block pattern with ST-segment elevation in the right precordial leads. The right bundle branch block may be incomplete while the ST segment elevation is minimal.
Amal, Mattu +4 more
openaire +2 more sources
Brugada syndrome describes the syndrome of sudden cardiac death in the setting of the following electrocardiographic findings: right bundle branch block pattern with ST-segment elevation in the right precordial leads. The right bundle branch block may be incomplete while the ST segment elevation is minimal.
Amal, Mattu +4 more
openaire +2 more sources
Acta Cardiologica, 2009
The Brugada syndrome is an inherited cardiac disorder initially described in 1992 by Pedro and Josep Brugada, with variable electrocardiographic features characteristic of right bundle-branch block, persistent ST-segment elevation in the precordial leads (VI-V3) at rest and sudden cardiac death.
Ricardo O, Escárcega +4 more
openaire +2 more sources
The Brugada syndrome is an inherited cardiac disorder initially described in 1992 by Pedro and Josep Brugada, with variable electrocardiographic features characteristic of right bundle-branch block, persistent ST-segment elevation in the precordial leads (VI-V3) at rest and sudden cardiac death.
Ricardo O, Escárcega +4 more
openaire +2 more sources
Current Opinion in Cardiology, 2002
The Brugada syndrome describes a subgroup of patients at risk for the occurrence of ventricular fibrillation who have no definable structural heart disease associated with a right bundle branch block conduction pattern and ST-segment elevation in the right precordial leads.
Gerald V, Naccarelli +3 more
openaire +2 more sources
The Brugada syndrome describes a subgroup of patients at risk for the occurrence of ventricular fibrillation who have no definable structural heart disease associated with a right bundle branch block conduction pattern and ST-segment elevation in the right precordial leads.
Gerald V, Naccarelli +3 more
openaire +2 more sources
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
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
Understanding Brugada syndrome
Journal of the American Academy of Physician Assistants, 2015Brugada syndrome is an established cause of sudden cardiac arrest in patients without structural cardiac abnormalities. Recognition and diagnosis of this syndrome has been slowly increasing. Syncope, ventricular dysrhythmia, or sudden cardiac arrest may be the presenting symptom, although detection of the characteristic right precordial ST-segment ...
Janine Mary, Gehshan, Denise, Rizzolo
openaire +2 more sources
Brugada Syndrome or Brugada Mimicry?
2004The 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
1993
Excerpt Disease characteristics. Brugada syndrome is characterized by ST-segment abnormalities in leads V1-V3 on ECG and a high risk of ventricular arrhythmias and sudden death. Brugada syndrome presents primarily during adulthood; age at diagnosis ranges from two days to 85 years. The mean age of sudden death is approximately 40 years.
Brugada, R. +3 more
openaire +1 more source
Excerpt Disease characteristics. Brugada syndrome is characterized by ST-segment abnormalities in leads V1-V3 on ECG and a high risk of ventricular arrhythmias and sudden death. Brugada syndrome presents primarily during adulthood; age at diagnosis ranges from two days to 85 years. The mean age of sudden death is approximately 40 years.
Brugada, R. +3 more
openaire +1 more source