Cargando…

Genetic and Molecular Mechanisms in Brugada Syndrome

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. Despite recent advances, it remains a complex condition, encompassing mechanisms, genetics, dia...

Descripción completa

Detalles Bibliográficos
Autores principales:	Moras, Errol, Gandhi, Kruti, Narasimhan, Bharat, Brugada, Ramon, Brugada, Josep, Brugada, Pedro, Krittanawong, Chayakrit
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10340412/ https://www.ncbi.nlm.nih.gov/pubmed/37443825 http://dx.doi.org/10.3390/cells12131791

Ejemplares similares

Brugada Syndrome: The Syndrome of Right Bundle Branch Block, ST segment Elevation in V(1) to V(3) and Sudden Death
por: Brugada, Josep, et al.
Publicado: (2001)

Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
por: Campuzano, Oscar, et al.
Publicado: (2020)

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
por: Allegue, Catarina, et al.
Publicado: (2015)

Use of intravenous antiarrhythmics to identify concealed Brugada syndrome
por: Brugada, Ramon
Publicado: (2000)

Anaesthetic management of patients with Brugada syndrome
por: Dendramis, Gregory, et al.
Publicado: (2018)

Brugada Syndrome in Women: What Do We Know After 30 Years?
por: Martínez-Barrios, Estefanía, et al.
Publicado: (2022)

The challenges of performing ajmaline challenge in children with suspected Brugada syndrome
por: Conte, Giulio, et al.
Publicado: (2014)

The Known Into the Unknown: Brugada Syndrome and COVID-19
por: Sorgente, Antonio, et al.
Publicado: (2020)

Experimental Models of Brugada syndrome
por: Sendfeld, Franziska, et al.
Publicado: (2019)

Genetics of channelopathies associated with sudden cardiac death
por: Campuzano, Oscar, et al.
Publicado: (2015)

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort
por: Selga, Elisabet, et al.
Publicado: (2015)

Appropriate and inappropriate therapies in remotely monitored patients with Brugada syndrome: what to expect?
por: Dendramis, Gregory, et al.
Publicado: (2023)

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances
por: Fernández-Falgueras, Anna, et al.
Publicado: (2017)

Large Genomic Imbalances in Brugada Syndrome
por: Mademont-Soler, Irene, et al.
Publicado: (2016)

Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation
por: Campuzano, Oscar, et al.
Publicado: (2020)

Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review
por: Oliva, Antonio, et al.
Publicado: (2022)

Recurrent cardiac events in patients with idiopathic ventricular fibrillation, excluding patients with the Brugada syndrome
por: Champagne, Jean, et al.
Publicado: (2005)

Topiramate induced type 1 Brugada pattern
por: Marchese, Procolo, et al.
Publicado: (2021)

Recent Advances in Short QT Syndrome
por: Campuzano, Oscar, et al.
Publicado: (2018)

Ablation of a life-threatening arrhythmia in a patient with Brugada syndrome
por: Kamel, Omnia, et al.
Publicado: (2021)

Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies
por: Grassi, Simone, et al.
Publicado: (2021)

Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population
por: Martínez-Barrios, Estefanía, et al.
Publicado: (2022)

Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology
por: Campuzano, Oscar, et al.
Publicado: (2014)

Epicardial mapping and ablation of the right ventricle substrate during flecainide testing in Brugada syndrome
por: Gonzalez-Melchor, Laila, et al.
Publicado: (2015)

Transient appearance of Brugada-like Type 1 electrocardiogram pattern immediately after biphasic synchronized electrical cardioversion for atrial fibrillation: a case series
por: Abdalla, Khalid A S, et al.
Publicado: (2019)

Speckle tracking echocardiography data in Brugada syndrome patients
por: Scheirlynck, Esther, et al.
Publicado: (2019)

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants
por: Pinsach-Abuin, Mel·lina, et al.
Publicado: (2021)

Postural Orthostatic Tachycardia Syndrome in COVID-19: A Contemporary Review of Mechanisms, Clinical Course and Management
por: Narasimhan, Bharat, et al.
Publicado: (2023)

Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome
por: Grassi, Simone, et al.
Publicado: (2022)

Electrocardiographic Assessment and Genetic Analysis in Neonates: A Current Topic of Discussion
por: Sarquella-Brugada, Georgia, et al.
Publicado: (2019)

Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes
por: Campuzano, Oscar, et al.
Publicado: (2020)

Electrocardiographic “Northwest QRS Axis” in the Brugada Syndrome: A Potential Marker to Predict Poor Outcome
por: Pérez-Riera, Andrés Ricardo, et al.
Publicado: (2020)

Short QT and atrial fibrillation: A KCNQ1 mutation–specific disease. Late follow-up in three unrelated children
por: Sarquella-Brugada, Georgia, et al.
Publicado: (2015)

Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation
por: Sarquella-Brugada, Georgia, et al.
Publicado: (2021)

Molecular autopsy in sudden cardiac death
por: Campuzano, Oscar, et al.
Publicado: (2023)

Endurance sport practice as a risk factor for atrial fibrillation and atrial flutter
por: Mont, Lluís, et al.
Publicado: (2009)

Update on the Genetic Basis of Sudden Unexpected Death in Epilepsy
por: Coll, Monica, et al.
Publicado: (2019)

Age and genetics are associated with ventricular fibrillation but not with monomorphic ventricular tachycardia in Brugada syndrome
por: Pannone, L, et al.
Publicado: (2023)

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants
por: Campuzano, Oscar, et al.
Publicado: (2019)

Trafficking and Function of the Voltage-Gated Sodium Channel β2 Subunit
por: Cortada, Eric, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_8om3u1gclb9ci8inicsi75084q