Results 61 to 70 of about 18,700 (219)

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, Hussain Moafa, Faleh Al-Qahtani, Tahir Hameed   +3 more
doaj   +1 more source

Brugada phenocopy secondary to hyperkalemia and hyponatremia in primary adrenal insufficiency

Journal of the American College of Emergency Physicians Open, 2022
Introduction The Brugada phenocopy represents electrocardiogram (ECG) changes nearly identical to the Brugada syndrome but without the congenital abnormality associated with lethal arrhythmias and normalizes with treatment of the underlying etiology ...
Olga Amusina, Sandeep Mehta, Michael E. Nelson   +2 more
doaj   +1 more source

Clinical Outcomes After Catheter Ablation in Patients With Structural Heart Disease and Ventricular Fibrillation

Journal of Cardiovascular Electrophysiology, EarlyView.
ABSTRACT Introduction In patients with ischemic cardiomyopathy (ICM), recurrent VF may be treated with catheter ablation by targeting triggering premature ventricular complexes (PVCs) and/or ventricular scar homogenization. Data on optimal ablation strategies in patients with non‐ischemic cardiomyopathy (NICM) remain limited.
Kenji Hashimoto, Samual Turnbull, Saurabh Kumar   +2 more
wiley   +1 more source

Detection of a Brugada syndrome in a occupational medical examination [PDF]

, 2011
Artículos originales[ES] El síndrome de Brugada es una cardiopatía genética y no estructural debida a una alteración primaria de los canales iónicos del miocardio y que se asocia a un riesgo de muerte súbita.
Sanz-Gallén, Pere, Ruíz, Mª Isabel, Mont, Lluis, Berne, Paola, Brugada, Josep, Marín, Eva, Nogüe, Santiago   +6 more
core   +1 more source

Whole‐Exome Sequencing Identifies a Rare CSRP3 Variant Associated With Familial Brugada Syndrome in a Lebanese Family

Journal of Cardiovascular Electrophysiology, EarlyView.
ABSTRACT Introduction Brugada syndrome (BrS) is an inherited arrhythmia associated with an increased risk of sudden cardiac death. Although traditionally regarded as a primary cardiac channelopathy, pathogenic variants in SCN5A account for only 20%–30% of clinically diagnosed cases, leaving most patients genetically unresolved.
Zainab Bashir, Ayat Kadhi, Jad Ballout, Bushra Samara, Maurice Khoury, Georges Nemer, Marwan Refaat   +6 more
wiley   +1 more source

Neurocardiac crosstalk in inherited cardiac arrhythmias and cardiomyopathy

The Journal of Physiology, EarlyView.
Abstract figure legend In inherited cardiac arrhythmias and cardiomyopathy, arrhythmias are typically triggered by autonomic nervous system activity. Genetic mutations linked to these conditions cause pro‐arrhythmic alterations in both cardiomyocytes and neurons, with their pathophysiological crosstalk likely amplifying the manifestation of the disease.
Carol Ann Remme, Molly O'Reilly
wiley   +1 more source

Brugada syndrome: 1992–2002 A historical perspective

, 2003
An intriguing new clinical entity characterized by ST-segment elevation in the right precordial electrocardiographic leads and a high incidence of sudden death in individuals with structurally normal hearts was described by Pedro and Josep Brugada in ...
Pedro Brugada, Nademanee, Kolawanee, Kolawanee Nademanee, Josep Brugada, Antzelevitch, Charles, Brugada, Ramon, Charles Antzelevitch, Ramon Brugada, Jeffrey A Towbin, Brugada, Josep, Brugada, Pedro, Towbin, Jeffrey A   +11 more
core   +1 more source

Brugada-fenokópia [PDF]

, 2016
Absztrakt A Brugada-fenokópia egy megkülönböztető új fogalma a Brugada-EKG-t utánzó kórképeknek. A Brugada-fenokópia jellemzője, hogy ha a kiváltó okot megszüntetjük, megszűnik az EKG-eltérés is.
János Tomcsányi, Tomcsányi, János
core   +1 more source

Proposed diagnostic criteria for the Brugada syndrome - Consensus report

, 2002
Asyndrome characterized by ST-segment elevation in right precordial leads (V1 to V3) that is unrelated to ischemia, electrolyte disturbances, or obvious structural heart disease was reported as early as 1953,1 but was first described as a distinct ...
BRUGADA J, BORGGREFE M, NADEMANEE K, HAUER RNW, PRIORI SG, TOWBIN JA, BRUGADA R, CORRADO, DOMENICO, ANTZELEVITCH C, KASS RS, WILDE AAM, BRUGADA P   +11 more
core   +1 more source

Brugada Syndrome: The Syndrome of Right Bundle Branch Block, ST segment Elevation in V1 to V3 and Sudden Death.

Indian Pacing and Electrophysiology Journal, 2001
In 1992 a new syndrome consisting of syncopal episodes and/or sudden death in patients with a structurally normal heart and a characteristic electrocardiogram (ECG) with a pattern of right bundle branch block with an ST segment elevation in leads V1 to ...
Josep Brugada, Pedro Brugada, Ramon Brugada   +2 more
doaj