Results 31 to 40 of about 2,202,317 (252)
Circulation Genomic and Precision Medicine, 2020 Supplemental Digital Content is available in the text. Background: Brugada syndrome (BrS) is characterized by the type 1 Brugada ECG pattern. Pathogenic rare variants in SCN5A (mutations) are identified in 20% of BrS families in whom incomplete ...
Y. Wijeyeratne +44 more
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The Relations of Brugada ECG Pattern and Fraqmented QRS in Patient with Schizophrenia
Sakarya Tıp Dergisi, 2021 Objective: Schizophrenia is a psychiatric disease with high risk of fatal rhythm disorders and sudden cardiac death. A previous study reported that Brugada syndrome was highly prevelant in patients with schizophrenia.
Ahmet Kaya +3 more
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Methodist DeBakey Cardiovascular Journal, 2014 Brugada syndrome is a rare cardiac arrhythmia characterized by electrocardiographic right bundle branch block and persistent ST-segment elevation in the right precordial leads. It is associated with ventricular fibrillation and a high risk for sudden cardiac death, predominantly in younger males with structurally normal hearts.
Brugada, R. +4 more
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Clinical features of Brugada syndrome
Journal of Arrhythmia, 2013 Brugada syndrome is a clinical entity characterized by type-1 (coved) ST-segment elevation in the right precordial electrocardiographic leads (V1–V3) and an aborted sudden cardiac death due to ventricular fibrillation (VF) in the absence of structural ...
Wataru Shimizu, MD, PhD
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Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations
Journal of Biomedical Science, 2009 The Brugada syndrome is characterized by ST segment elevation in the right precodial leads V1-V3 on surface ECG accompanied by episodes of ventricular fibrillation causing syncope or even sudden death.
Juang Jyh-Ming +8 more
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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
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BRUGADA SYNDROME: FROM PRIMARY ELECTRIC HEART DISEASE TO MORPHOLOGICAL SUBSTRATE
Архивъ внутренней медицины, 2016 Nowadays interest in channelopathies is growing, and developing diagnostic capabilities make Brugada syndrome much more actual problem than ever. Conception of «primary electric heart disease», which earlier was so popular, now couldn’t explain the ...
T. A. Pavlenko, O. V. Blagova
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Mechanisms of Arrhythmias in the Brugada Syndrome
International Journal of Molecular Sciences, 2020 Arrhythmias in Brugada syndrome patients originate in the right ventricular outflow tract (RVOT). Over the past few decades, the characterization of the unique anatomy and electrophysiology of the RVOT has revealed the arrhythmogenic nature of this ...
M. Blok, B. Boukens
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Journal of Arrhythmia, 2016 AbstractIn 1992, the Brugada syndrome (BrS) was recognized as a disease responsible for sudden cardiac death, characterized by a right bundle‐branch block with ST segment elevation in the leads V1 and V2. This syndrome is highly associated with sudden cardiac death, especially in young males.
Juang, Jyh-Ming Jimmy, Horie, Minoru
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Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease, 2020 Background A combination of clinical and electrocardiographic risk factors is used for risk stratification in Brugada syndrome. In this study, we tested the hypothesis that the incorporation of latent variables between variables using nonnegative matrix ...
G. Tse +13 more
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