Results 51 to 60 of about 510 (152)

Brugada phenocopies are the leading differential diagnosis of Brugada syndrome [PDF]

open access: yesClinical Medicine, 2015
OVERVIEW Please submit letters for the editor9s consideration within three weeks of receipt of Clinical Medicine.
Byron H, Gottschalk   +2 more
openaire   +2 more sources

Rhabdomyoma of the interventricular septum presenting as a Brugada phenocopy [PDF]

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

Fenocopia de Brugada en el contexto de una infección severa por COVID-19 [PDF]

open access: yes, 2021
Las fenocopias de Brugada son un patrón electroctrocardiográfico con igual morfología a los patrones del Síndrome de Brugada tipo 1 y 2, en pacientes con alteraciones metabólicas, isquémicas y/o mecánicas.
de la Torre Fonseca, Luis Mariano   +2 more
core   +1 more source

Brugada ECG phenocopy in hypertrophic cardiomyopathy: The time matter [PDF]

open access: yes, 2023
An Implantable Cardioverter-Defibrillator was implanted in an asymptomatic 56-year-old man, with type 2 Brugada pattern on ECG, inducible ventricular fibrillation at elective electrophysiological study, and a family history of sudden cardiac death ...
Bernardelli A.   +5 more
core   +1 more source

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

Data_Sheet_1_Case Report: Coexistent Wolff-Parkinson-White Syndrome and Brugada Phenocopy in a Patient With Pneumonia and Myocarditis.zip [PDF]

open access: yes, 2021
Background: In recent years, Wolff-Parkinson-White (WPW) syndrome and Brugada electrocardiogram (ECG) patterns have been reported as coexistent in the same patient. In most cases, the two waveforms appeared separately.
Yana Zhao (7004009)   +2 more
core   +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

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

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

Home - About - Disclaimer - Privacy