Publicaciones
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Martínez-Barrios E, Greco A, Cruzalegui JC, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Slanovic L, Mangas A, Toro R, Brugada-Terradellas J, Sarquella-Brugada G and Campuzano O.
Interpreting the actionable clinical role of rare variants associated with short QT syndrome.
HUMAN GENETICS . 143(12): 1499-1508.
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Bazan V, Arana E, Rubio-Campal JM, Calvo D, Álvarez Acosta L, Hernández Afonso J, Ramos Ardanaz P, Peñafiel Verdú P, Cano Calabria LR, Barrera Cordero A, Díaz Infante E, Cózar León R, Lozano Granero VC, Martínez Sande JL, Moya Mitjans À, Rodríguez Entem F, Salgado Aranda R, Gil Ortega I, Cabanas Grandío P, Alcalde Rodriguez Ó, García Fernández FJ, Sarquella-Brugada G, Castro Urda V, Fidalgo Andrés ML, Durán Guerrero JM, Mazuelos Bellido F, Rubio Caballero JA, Pérez Roselló V, Cabrera Ramos M, Rubio Campal JM, Porta Sánchez A, Hidalgo Olivares VM, Rubín López JM, Jiménez López J, Grande Morales CE, Fernández Gómez JM, Jiménez Candil J, Moreno Garrido R, Rodríguez Muñoz D, Vázquez Esmorís I, Ibáñez Criado JL, Ibáñez Criado A, Arcocha Torres MF, Bastos Amador P, Elices Teja J, Pavón Jiménez R, Martín Sánchez G, Benezet Mazuecos J, Arce León A, Quesada Dorador A, Mendoza Lemes H, Herreros Guilarte B, Osca Asensi J, Datino Romaniega T, Sarrias A, Ferrer Hita JJ, Lozano Herrera JM, Ángel Arias M, Rivas Gandara N, Sánchez Borque P, García Cuenca E, Bochard Villanueva B, Alonso Fernández P, Valverde André I, Moraleda Salas MT, Sandín Fuentes MG, Pastor Fuentes A, Portales Fernández J, Ruiz Hernández PM, Guasch Casany E, Pedrote A, Asso Abadía A, Guerra Ramos JM, Anguera I, Cantalapierda J, Sainz Godoy Í, Domínguez Mafé E, Rodriguez Font E, Martí Almor J, Moreno Arribas J, Merino Llorens JL, Bertomeu González V, Benito Martín EM, Mosquera Pérez I, Álvarez López M, Peláez González A, Jiménez Díaz FJ, Saurí Ortiz A, Luque Lezcano AÓ, Segura Villalobos F, Almendral Garrote J, Salvador Montañés Ó, González Ferrer JJ, Gómez Pulido F, Peinado Peinado R, Fabregat Andrés Ó, Arenal Á, Moreno S and Del Castillo ÁM.
Spanish catheter ablation registry. 23rd official report of the Heart Rhythm Association of the Spanish Society of Cardiology (2023).
REVISTA ESPANOLA DE CARDIOLOGIA . 77(12): 1026-1036.
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Martínez-Barrios E, Greco A, Cruzalegui JC, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Fogaça-da-Mata M, Díez-López C, Arbelo E, Grassi S, Oliva A, Toro R, Sarquella-Brugada G and Campuzano O.
Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis.
Biomedicines . 12(11): .
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de Frutos F, Ochoa JP, Webster G, Jansen M, Remior P, Rasmussen TB, Sabater-Molina M, Barriales-Villa R, Girolami F, César-Díaz S, Fuentes-Cañamero ME, Alvarez García-Rovés R, Wahbi K, Limeres J, Kubanek M, Slieker MG, Sarquella-Brugada G, Abrams DJ, Dooijes D, Domínguez F and Garcia-Pavia P.
Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy.
JOURNAL OF THE AMERICAN HEART ASSOCIATION . 13(21): .
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Martínez-Barrios E, Campuzano O, Greco A, Cruzalegui JC and Sarquella-Brugada G.
Cardiac channelopathies in pediatrics: a genetic update.
EUROPEAN JOURNAL OF PEDIATRICS . 183(11): 4635-4640.
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Lamba A, Roston TM, Peltenburg PJ, Kallas D, Franciosi S, Lieve KVV, Kannankeril PJ, Horie M, Ohno S, Brugada R, Aiba T, Fischbach P, Knight L, Till J, Kwok SY, Probst V, Backhoff D, LaPage MJ, Batra AS, Drago F, Haugaa K, Krahn AD, Robyns T, Swan H, Tavacova T, Atallah J, Borggrefe M, Rudic B, Sarquella-Brugada G, Chorin E, Hill A, Kammeraad J, Kamp A, Law I, Perry J, Roberts JD, Tisma-Dupanovic S, Semsarian C, Skinner JR, Tfelt-Hansen J, Denjoy I, Leenhardt A, Schwartz PJ, Ackerman MJ, Wilde AAM, van der Werf C and Sanatani S.
An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia.
Heart Rhythm . 21(10): 1767-1776. Nº de citas: 3
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Bergonti M, Ciconte G, Cruzalegui JC, Crotti L, Arbelo E, Casella M, Saenen J, Rossi A, Pannone L, Martínez-Barrios E, Compagnucci P, Russo V, Berne P, Van Leuven O, Boccellino A, Marcon L, Dagradi F, Landra F, Özkartal T, Comune A, Conti S, Ribatti V, Campuzano O, Brugada P, de Asmundis C, Brugada J, Pappone C, Tondo C, Schwartz PJ, Auricchio A, Sarquella-Brugada G and Conte G.
Continuous Rhythm Monitoring With Implanted Loop Recorders in Children and Adolescents With Brugada Syndrome
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 84(10): 921-933. Nº de citas: 4
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Camiña-Conforto G, Ivars M, Sarquella-Brugada G, Carlos Valera Dávila, Salvador-Hernandez H, Rovira-Zurriaga C and Baselga E.
Phacomatosis pigmentokeratotica: Exploring extracutaneous comorbidities and topical therapy.
PEDIATRIC DERMATOLOGY . 41(5): 904-907.
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Bonet, F, Campuzano, O, Cordoba-Caballero, J, Alcalde, M, Sarquella-Brugada G, Braza-Boils, A, Brugada, R, Hernandez-Torres, F, Quezada-Feijoo, M, Ramos, M, Mangas, A, Ranea, JAG and Toro, R.
Role of miRNA-mRNA Interactome in Pathophysiology of Arrhythmogenic Cardiomyopathy
Biomedicines . 12(8): .
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Sarquella-Brugada G, Martínez-Barrios E, César-Díaz S, Toro R, Cruzalegui JC, Greco A, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Arbelo E, Diez-López C, Grazioli G, Balderrábano N and Campuzano O.
A narrative review of inherited arrhythmogenic syndromes in young population: role of genetic diagnosis in exercise recommendations.
BMJ OPEN SPORT & EXERCISE MEDICINE . 10(3): .