Results 11 to 20 of about 16,632 (223)
Journal of the Saudi Heart Association, 2016 Brugada syndrome (BS), a life-threatening channelopathy associated with reduced inward sodium current due to dysfunctional sodium channels, is characterized by ST-segment elevation with downsloping “coved type” (type 1) or “saddle back” (type 2) pattern ...
Yashwant Agrawal +3 more
doaj +3 more sources
Suspected hyponatremia-induced Brugada phenocopy [PDF]
International Medical Case Reports Journal, 2019 Koomatie Ramsaroop,1 Rajeev Seecheran,1 Valmiki Seecheran,1 Sangeeta Persad,1 Stanley Giddings,2 Boris Mohammed,1 Naveen Anand Seecheran2 1Department of Medicine, North Central Regional Health Authority, Mt Hope, Trinidad and Tobago; 2Department of ...
Ramsaroop K +6 more
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A Case of Brugada Syndrome… or Something Else? Behind Type 1 Brugada Pattern. [PDF]
Clin Case RepABSTRACT Although Brugada syndrome has traditionally been considered a primary electrical disease, accumulating evidence supports the presence of subtle structural abnormalities, particularly involving the right ventricular outflow tract. Nevertheless, the identification of overt myocardial scar and biventricular arrhythmogenic substrate should prompt ...
Scarà A +3 more
europepmc +2 more sources
Acta Cardiologica, 2020 Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome that causes a heightened risk for ventricular tachyarrhythmias and sudden cardiac death. BrS is characterised by a coved ST-segment elevation in right precordial leads. The prevalence is estimated to range between 1 in 5,000 to 1 in 2,000 in different populations, with the highest being
Korlipara, Haarika +2 more
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Prevalence of Brugada-type ECG pattern and early ventricular repolarization pattern in Tunisian athletes [PDF]
Open Access Journal of Sports Medicine, 2011 Sana Ouali1, Helmi Ben Salem1, Sami Hammas1, Elyes Neffeti1, Fahmi Remedi1, Abdallah Mahdhaoui2, Essia Boughzela1, Rafik Mankai31Department of Cardiology, Sahloul Hospital, Sousse, Tunisia; 2Department of Cardiology, Farhat Hached, Sousse, Tunisia ...
Ouali S +7 more
doaj +1 more source
Genetic and Molecular Mechanisms in Brugada Syndrome [PDF]
, 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
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Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A [PDF]
, 2020 Background: A 30-year-old man presented with intellectual disability associated with epilepsy. The epilepsy was initially treated with sodium valproate and since he was 28 years-old with lamotrigine. With the addition of lamotrigine, a pattern of Brugada
Banfi P. +9 more
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JACC: Clinical Electrophysiology, 2022 Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and cardiac arrest, predominantly during sleep. The prevalence is ∼1:2,000, and is more commonly diagnosed in young to middle-aged males, although patient sex does not appear to impact prognosis.
Krahn, AD +5 more
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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
openaire +6 more sources
Featuring: Josep Brugada [PDF]
, 2019 In the Cardiology Masters section of European Cardiology Review, we bring you an insight into the career of a key contributor to the field of cardiology.
Josep Brugada
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