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Use, misuse, and pitfalls of the drug challenge test in the diagnosis of the Brugada syndrome
European Heart Journal, 2023 Graphical Abstract Graphical Abstract Use, misuse, and pitfalls of the drug challenge test in the diagnosis of the Brugada syndrome. *Diagnosis of Brugada syndrome is based on the modified Shanghai criteria (see Table 2).
A. Wilde, A. Amin, H. Morita, R. Tadros
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Genetic and Molecular Mechanisms in Brugada Syndrome
Cells, 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.
E. Moras +6 more
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The Genetics of Brugada Syndrome.
Annual review of genomics and human genetics (Print), 2022 Brugada syndrome is a heritable channelopathy characterized by a peculiar electrocardiogram (ECG) pattern and increased risk of cardiac arrhythmias and sudden death.
M. Cerrone, S. Costa, M. Delmar
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European Heart Journal, 2021 Brugada syndrome (BrS) was first described as a primary electrical disorder predisposing to the risk of sudden cardiac death and characterized by right precordial lead ST elevation.
E. Behr +4 more
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Clinical presentation and electrocardiographic features of Brugada syndrome in Iraq [PDF]
The Medical Journal of Basrah University, 2021 Background: Brugada syndrome is a clinical entity composed of twelve leads electrocardiographic changes of coved or saddle shaped ST-segment elevation in V1 and V2 with serious ventricular arrhythmias which may cause sudden cardiac death. Objectives: The
AMAR AL-HAMDI
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The Unmasking Effect: Propofol-Induced Brugada Pattern in a Critically Ill Patient
Case Reports in Cardiology, 2022 Brugada syndrome is a known cause of dysrhythmias and sudden cardiac death. It is linked to mutations in myocardial sodium channel leading to hyperexcitable cardiac myocytes.
Esiemoghie Akhigbe +4 more
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Does the Age of Sudden Cardiac Death in Family Members Matter in Brugada Syndrome?
Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease, 2021 Background Brugada syndrome is an inherited cardiac channelopathy associated with major arrhythmic events (MAEs). The presence of a positive family history of sudden cardiac death (SCD) as a risk predictor of MAE remains controversial.
P. Rattanawong +11 more
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Model of nursing care for patients with Brugada syndrome according to the international ICNP®
Journal of Education, Health and Sport, 2019 Introduction Brugada syndrome is a rare disease involving genetic disorders of heart rhythm. The disease was discovered in 1992 by the Brugada brothers, Spanish cardiologists.
Aleksandra Stosiek +3 more
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Brugada pattern in adolescent with acute myocarditis due to SARS‐CoV‐2
Journal of the American College of Emergency Physicians Open, 2022 Brugada syndrome is a genetic disorder characterized by abnormal findings on electrocardiogram (ECG) that can precipitate ventricular tachyarrhythmias and sudden cardiac death.
David Bergamo, Courtney Nelson
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International Journal of Molecular Sciences, 2021 Brugada syndrome and early repolarization syndrome are both classified as J-wave syndromes, with a similar mechanism of arrhythmogenesis and with the same basis for genesis of the characteristic electrocardiographic features.
B. Boukens, M. Potse, R. Coronel
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