Results 21 to 30 of about 2,471,143 (310)
Orphanet Journal of Rare Diseases, 2006 A novel clinical entity characterized by ST segment elevation in right precordial leads (V1 to V3), incomplete or complete right bundle branch block, and susceptibility to ventricular tachyarrhythmia and sudden cardiac death has been described by Brugada et al. in 1992. This disease is now frequently called "Brugada syndrome" (BrS).
Napolitano C, PRIORI, SILVIA GIULIANA
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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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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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Enhancing rare cardiac disease classification with GAN-augmented supervised and self-supervised learning: a case study on Brugada syndrome [PDF]
Eur Heart J Digit HealthB Zanchi, G Monachino, G Conte, F Faraci
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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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Prognostic Value of Small Coved-Type ST-Segment Area in Patients With Spontaneous Type 1 Brugada Syndrome. [PDF]
J Cardiovasc ElectrophysiolElectrical and structural abnormalities in Brugada syndrome lead to a smaller coved‐type ST‐segment area. A reduced ST‐segment area may identify patients at elevated risk of ventricular fibrillation. ABSTRACT Background Risk stratification in Brugada syndrome (BrS) remains challenging.
Sano N +10 more
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Revista Española de Cardiología (English Edition), 2008 Since its first description in 1992 as a new clinical entity, the Brugada syndrome has aroused great interest among physicians and basic scientists. Two consensus conferences held in 2002 and 2005 helped refine the current accepted definite diagnostic criteria for the syndrome, briefly, the characteristic ECG pattern (right bundle branch block and ...
Benito, B. +3 more
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The Lancet, 2002 The Brugada syndrome has gained wide recognition throughout the world and today is believed to be responsible for 4% to 12% of all sudden deaths and ≈20% of deaths in patients with structurally normal hearts. The incidence of the disease is on the order of 5 per 10 000 inhabitants and, apart from accidents, is the leading cause of death of men under ...
S R, Vavricka +2 more
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Brugada syndrome in a 4-year-old child with Lemierre syndrome—A case report
Journal 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
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Cardiac Electrophysiology Review, 1999 The Brugada syndrome is a genetically determined disease caused by mutations of the cardiac sodium channel. The disease affects mainly males in their forties and causes sudden cardiac death because of polymorphic ventricular tachycardia. These patients have a structurally normal heart.
Brugada, Pedro, Brugada, J., Brugada, R.
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