Publicaciones
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Martínez-Barrios E, Greco A, César-Díaz S, Díez-López C, Cruzalegui JC, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Grassi S, Oliva A, Balderrábano N, Toro R, Sarquella-Brugada G and Campuzano O.
Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes.
iScience . 28(5): 112300-112300.
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Zanchi, B, Monachino, G, Faraci, FD, Metaldi, M, Brugada, P, Sarquella-Brugada G, Behr, ER, Brugada-Terradellas J, Crotti, L, Belhassen, B and Conte, G.
Synthetic electrocardiograms for Brugada syndrome: from data generation to expert cardiologists evaluation
european heart journal - digital health . : .
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Behr ER, Winkel BG, Ensam B, Alfie A, Arbelo E, Berry C, Cerrone M, Conte G, Crotti L, Corcia CMG, Kaski JC, Nademanee K, Postema PD, Priori S, Probst V, Sarquella-Brugada G, Schulze-Bahr E, Tadros R, Wilde A and Tfelt-Hansen J.
The diagnostic role of pharmacological provocation testing in cardiac electrophysiology: a clinical consensus statement of the European Heart Rhythm Association and the European Association of Percutaneous Cardiovascular Interventions (EAPCI) of the ESC, the ESC Working Group on Cardiovascular Pharmacotherapy, the Association of European Paediatric and Congenital Cardiology (AEPC), the Paediatric & Congenital Electrophysiology Society (PACES), the Heart Rhythm Society (HRS), the Asia Pacific Heart Rhythm Society (APHRS), and the Latin American Heart Rhythm Society (LAHRS).
Europace . 27(4): .
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Greco A, Martínez-Barrios E, Cruzalegui JC, César-Díaz S, Chipa, F, Nuria Díez Escuté, Patricia Cerralbo Martín, Zschaeck-Luzardo I, Loredo, P, Sarquella-Brugada G and Campuzano, O.
Brugada Syndrome and GPD1L: Definite Genotype-Phenotype Association?
cardiogenetics . 15(1): .
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Conte G, Bergonti M, Probst V, Morita H, Tfelt-Hansen J, Behr ER, Kengo K, Arbelo E, Crotti L, Sarquella-Brugada G, Wilde AAM, Calò L, Sarkozy A, de Asmundis C, Mellor G, Migliore F, Letsas K, Vicentini A, Levinstein M, Berne P, Chen SA, Veltmann C, Biernacka EK, Carvalho P, Kabawata M, Sojema K, Gonzalez MC, Tse G, Thollet A, Svane J, Caputo ML, Scrocco C, Kamakura T, Pardo LF, Lee S, Juárez CK, Martino A, Lo LW, Monaco C, Reyes-Quintero ÁE, Martini N, Oezkartal T, Klersy C, Brugada-Terradellas J, Schwartz PJ, Brugada P, Belhassen B and Auricchio A.
aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes: results from the TETRIS study
Europace . 26(12): . Nº de citas: 2
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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. Nº de citas: 2
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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, 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): . Nº de citas: 1
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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.