Georgia Sarquella-Brugada
Overview
Explore the profile of Georgia Sarquella-Brugada including associated specialties, affiliations and a list of published articles.
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143
Citations
2243
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Recent Articles
1.
Martinez-Barrios E, Greco A, Cruzalegui J, Cesar S, Diez-Escute N, Cerralbo P, et al.
Biomedicines
. 2024 Nov;
12(11).
PMID: 39595119
Inherited arrhythmogenic syndromes comprise a heterogenic group of genetic entities that lead to malignant arrhythmias and sudden cardiac death. Genetic testing has become crucial to understand the disease etiology and...
2.
Conte G, Bergonti M, Probst V, Morita H, Tfelt-Hansen J, Behr E, et al.
Europace
. 2024 Nov;
26(12).
PMID: 39527076
Aims: Little is known about the distribution and clinical course of patients with inherited arrhythmia syndrome (IAS) and concomitant atrial arrhythmias (AAs). The aim of the study is (i) to...
3.
Martinez-Barrios E, Greco A, Cruzalegui J, Cesar S, Diez-Escute N, Cerralbo P, et al.
Hum Genet
. 2024 Nov;
143(12):1499-1508.
PMID: 39503779
Genetic testing is recommended in the diagnosis of short QT syndrome. This rare inherited lethal entity is characterized by structural normal hearts with short QT intervals in the electrocardiogram. Few...
4.
de Frutos F, Ochoa J, Webster G, Jansen M, Remior P, Rasmussen T, et al.
J Am Heart Assoc
. 2024 Nov;
13(21):e036208.
PMID: 39494569
Background: Although genetic variants in are the most frequent cause of pediatric genetic dilated cardiomyopathy (DCM), there are no studies available describing this entity. We sought to describe clinical features,...
5.
Bazan V, Arana E, Rubio-Campal J, Calvo D, Alvarez Acosta L, Hernandez Afonso J, et al.
Rev Esp Cardiol (Engl Ed)
. 2024 Sep;
77(12):1026-1036.
PMID: 39313188
Introduction And Objectives: We report the results of the 2023 Spanish catheter ablation registry. Methods: Procedural data were collected and incorporated into the REDCap platform by all participating centers through...
6.
Martinez-Barrios E, Campuzano O, Greco A, Cruzalegui J, Sarquella-Brugada G
Eur J Pediatr
. 2024 Sep;
183(11):4635-4640.
PMID: 39307882
Cardiac channelopathies are a group of inherited syndromes that can cause malignant arrhythmias and sudden cardiac death, particularly in the pediatric population. Today, a 12-lead electrocardiogram is the most effective...
7.
Bonet F, Campuzano O, Cordoba-Caballero J, Alcalde M, Sarquella-Brugada G, Braza-Boils A, et al.
Biomedicines
. 2024 Aug;
12(8).
PMID: 39200271
Arrhythmogenic cardiomyopathy is an inherited entity characterized by irregular cell-cell adhesion, cardiomyocyte death and fibro-fatty replacement of ventricular myocytes, leading to malignant ventricular arrythmias, contractile dysfunction and sudden cardiac death....
8.
Bergonti M, Ciconte G, Cruzalegui Gomez J, Crotti L, Arbelo E, Casella M, et al.
J Am Coll Cardiol
. 2024 Aug;
84(10):921-933.
PMID: 39197982
Background: Young (<18 years of age) patients with Brugada syndrome (BrS) are often under-represented in BrS studies and their management, especially related to syncopal episodes, remains unclear. Objectives: This study...
9.
Sarquella-Brugada G, Martinez-Barrios E, Cesar S, Toro R, Cruzalegui J, Greco A, et al.
BMJ Open Sport Exerc Med
. 2024 Jul;
10(3):e001852.
PMID: 38975025
Sudden cardiac death is a rare but socially devastating event, especially if occurs in young people. Usually, this unexpected lethal event occurs during or just after exercise. One of the...
10.
Martinez Oloron P, Alegria I, Cesar S, Del Olmo B, Martinez-Barrios E, Carrera-Garcia L, et al.
Int J Mol Sci
. 2024 Jun;
25(11).
PMID: 38892025
Pathogenic variants in have been associated with a wide spectrum of muscular conditions: the laminopathies. -related congenital muscular dystrophy is a laminopathy characterised by the early onset of symptoms and...