Publications
-
Grassi S, Campuzano O, Ferri E, Leone G, Rossi R, Ortega-Sánchez M, Barberia E, Landin I, Arena V, Sarquella-Brugada G, Brugada R and Oliva A.
Forensic pathological and genetic landmarks in sudden cardiac death in the young: An update.
FORENSIC SCIENCE INTERNATIONAL-GENETICS . 80: 103334-103334.
-
Campuzano O, Grassi S, Martínez-Barrios E, Greco A, Arena V, Sarquella-Brugada G and Oliva A.
Brugada syndrome in the forensic field: what do we know to date?
frontiers in cardiovascular medicine . 12: 1618762-1618762.
-
Norrish G, Hall K, Field E, Cervi E, Boleti O, Ziólkowska L, Olivotto I, Passantino S, Khraiche D, Limongelli G, Weintraub RG, Anastasakis A, Biagini E, Ragni L, Sarquella-Brugada G, César-Díaz S, Prendiville T, McLeod K, Ilina M, Baban A, Ojala TH, Spentzou G, Bhole V, Gran F, Brown E, Delle Donne G, Khodaghalian B, Fernandez A, Daubeney PEF, Linter K, Kubus P, Uzun O, Bökenkamp R, Raimondi F, Marrone C, Medrano C, Gonzalez-Lopez E, Siles A, Luczak-Wozniak K, Bharucha T, Adwani S, Klaassen S, Castro FJ, Guereta L, Yamazawa H, Sinagra G, Popoiu A, Perin F, Chana B, De Wilde H, Rasmussen TB, Mogensen J, Mathur S, Centeno F, Reinhardt Z, Barriales-Villa R, Kubo T, Felice T, Radulescu C, Schouvey S, Chaker M and Kaski JP.
Sex Differences in Children and Adolescents With Hypertrophic Cardiomyopathy
JACC-ADVANCES . 4(8): 101907-101907.
-
Monda E, Biagini E, Blom N, Drago F, Krapels I, Krebsová A, Koubsky K, Khraiche D, Martins E, Merlo M, Michels M, Mizia-Stec K, Mörner S, Peña Peña ML, Planinc I, Robyns T, Rydberg A, Saenen J, Rodríguez Palomares JF, Rutger H, Sarquella-Brugada G, Scheirlynck E, Schulze-Bahr E, Tfelt-Hansen J, Wolf CM, Hofman N, Amin AS, Wilde A, Charron P and Limongelli G.
Current management of transition and multidisciplinary care of patients with inherited and rare cardiomyopathies in Europe: results of the European Reference Network for rare and low prevalence complex diseases of the heart
EUROPEAN HEART JOURNAL-QUALITY OF CARE AND CLINICAL OUTCOMES . : .
-
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 . 6(4): 683-687.
-
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. Number of citations: 1
-
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): . Number of citations: 5
-
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): .
-
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): . Number of citations: 2
-
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.