Results 51 to 60 of about 10,650 (163)

Brugada Phenocopy in a Child With Parvovirus B19 Myocarditis. [PDF]

open access: yesJACC Case Rep
Sodium channelopathies predispose to life-threatening arrhythmias. Brugada phenocopies (BrPs) are nongenetic conditions that mimic Brugada syndrome and may have a reversible cause.A 16-month-old child presented with a 12-day ventricular tachycardia storm and a spontaneous type 1 Brugada electrocardiogram pattern during sinus rhythm.
Bueno-Gomez A   +5 more
europepmc   +4 more sources

Brugada syndrome: should we be screening patients before prescribing psychotropic medication?

open access: yesTherapeutic Advances in Psychopharmacology, 2022
Brugada syndrome (BrS) presents with a characteristic electrocardiogram (ECG) and is associated with sudden cardiac death. Until now, prolongation of QTc interval and its association with Torsade de Pointe and possible fatal arrhythmia have been the ...
Azizah Attard   +4 more
doaj   +1 more source

A dynamic Brugada sign due to left anterior descending coronary artery occlusion

open access: yesIndian Pacing and Electrophysiology Journal, 2022
Brugada phenocopies (BrP) include several conditions with a common electrocardiographic (ECG) pattern that are indistinguishable from classical Brugada syndrome (BrS).
Vickram Vignesh Rangaswamy   +3 more
doaj   +1 more source

Featuring: Josep Brugada [PDF]

open access: yes, 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
core   +1 more source

Particular electrocardiographic phenotypes in acute coronary syndromes [PDF]

open access: yesRomanian Medical Journal, 2020
Despite continuous efforts in early recognition and timely management, acute coronary syndromes (ACS) continue to be the most common cause of death worldwide.
Anamaria Avram   +5 more
doaj   +1 more source

ECG Markers of Positive Drug Challenge With Ajmaline in Patients With Brugada Syndrome

open access: yesAnnals of Noninvasive Electrocardiology, Volume 31, Issue 1, January 2026.
A 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.
Erol Tülümen   +9 more
wiley   +1 more source

AN UNCOMMON STEMI MASQUERADER: A CASE OF IMIPRAMINE INDUCED BRUGADA PHENOCOPY (BRP)

open access: yes, 2022
Brugada syndrome(BrS) is an arrhythmogenic disorder characterized by a bulging ST-segment elevation and a J-point elevation of at least 2 mm in at least two of the right precordial electrocardiogram (ECG) leads (V1-3).
Kovvuri Hari Lalith Reddy , Gollapalli Sajit Kishan and A. Satyendra Kumar
core   +1 more source

Brugada phenocopy: A new electrocardiogram phenomenon

open access: yesWorld Journal of Cardiology, 2014
Brugada phenocopies (BrP) are clinical entities that are etiologically distinct from true congenital Brugada syndrome. BrP are characterized by type 1 or type 2 Brugada electrocardiogram (ECG) patterns in precordial leads V1-V3. However, BrP are elicited by various underlying clinical conditions such as myocardial ischemia, pulmonary embolism ...
Daniel D, Anselm   +2 more
openaire   +2 more sources

Biallelic Truncating Variants in SCN3B Encoding Nav Channel Subunit β3 Lead to Neurodevelopmental Phenotype with and without Epilepsy and Ataxia

open access: yesAnnals of Neurology, Volume 98, Issue 4, Page 864-870, October 2025.
SCN3B encodes the β3 auxiliary subunit, essential for voltage‐gated Na+ (Nav) channel trafficking and gating. Although SCN3B has been associated with cardiac disorders, a link with neurodevelopmental disorders (NDD) has not been established. Using a genotype‐first approach, we identified homozygous truncating variants (c.281G>A‐β3W94*, c.584 + 1G>A ...
Nathan Routledge   +11 more
wiley   +1 more source

Rhabdomyoma of the interventricular septum presenting as a Brugada phenocopy

open access: yes, 2011
Brugada syndrome is a channelopathy characterised electrocardiographically by distinctive coved ST-segment elevation in the right precordial leads and is associated with a predisposition for sudden death secondary to ventricular arrhythmias in otherwise ...
Adrian Baranchuk   +2 more
core   +1 more source

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