Results 11 to 20 of about 25,737 (250)
ECG Markers of Positive Drug Challenge With Ajmaline in Patients With Brugada Syndrome. [PDF]
Ann Noninvasive ElectrocardiolA prominent S‐wave in lead II on a nondiagnostic baseline ECG is a powerful predictor for unmasking Brugada syndrome during an ajmaline challenge. This subtle sign enhances patient selection for provocation testing and aids in risk stratification, particularly in familial screening.
Tülümen E +9 more
europepmc +2 more sources
Indian Heart Journal, 2017 Background: Ventricular fibrillation and atrial fibrillation are well-known arrhythmias in patients with Brugada syndrome. This study evaluated the characteristics of the atrial arrhythmogenic substrate using the signal-averaged electrogram (SAECG) in ...
Yasutsugu Nagamoto +12 more
doaj +1 more source
Reversible Brugada like electrocardiographic pattern in COVID-19 infection
Saudi Journal for Health Sciences, 2021 Brugada syndrome, a rare genetic disease increases the risk of arrhythmias and sudden cardiac death. Various trigger factors has been associated with Brugada syndrome. Arrhythmias have been reported in COVID 19. We report a patient with transient Brugada
Kamal Kant Jena +5 more
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Treatment of Electrical Storm with Amiodarone in Brugada Syndrome- an Unexpected Protective Effect [PDF]
, 2013 We are reporting on a 53 year old man with proven Brugada syndrome and ICD implantation for resuscitation in context of polymorphic VT. After recurrent arrhythmia he was treated with Amiodarone.
Lambiase, PD, Novak, J
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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
openaire +2 more sources
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
openaire +3 more sources
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
doaj +1 more source
Anesthesia in patients with Brugada syndrome: two case reports
Journal of Medical Case Reports, 2023 Background Brugada syndrome is a rare disease. It causes sudden cardiac arrest, which is a serious life-threatening event. Sudden cardiac death mostly results from coronary artery disease.
Che-Hao Hsu, Shin-Hong Lin, Li-Yen Chang
doaj +1 more source
Speckle tracking echocardiography data in Brugada syndrome patients
Data in Brief, 2019 Brugada syndrome is characterized by typical electrocardiogram changes and a high risk for sudden cardiac death (Priori et al., 2013). In addition to the well known electrical substrate, morphological and functional alterations appeared to be present in ...
Esther Scheirlynck +9 more
doaj +1 more source
Genetics update: monogenetics, polygene disorders and the quest for modifying genes [PDF]
, 2018 The genetic channelopathies are a broad collection of diseases. Many ion channel genes demonstrate wide phenotypic pleiotropy, but nonetheless concerted efforts have been made to characterise genotype-phenotype relationships.
Symonds, Joseph D., Zuberi, Sameer M.
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