Publicacions
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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. Nº de cites: 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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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. Nº de cites: 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. Nº de cites: 1
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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 cites: 2
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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): . Nº de cites: 3
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Fogaça-da-Mata M, Martínez-Barrios E, Jiménez-Montañés L, Cruzalegui JC, Chipa-Ccasani F, Greco A, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Zschaeck-Luzardo I, Clavero Adell M, Ayerza-Casas A, Palanca-Arias D, López M, Campuzano O, Brugada-Terradellas J and Sarquella-Brugada G.
Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?
Genes . 15(5): . Nº de cites: 1
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Coccia, E, Valeri, L, Zuntini, R, Caraffi, SG, Peluso, F, Pagliai, L, Vezzani, A, Pietrangiolillo, Z, Leo, F, Melli, N, Fiorini, V, Greco A, Lepri, FR, Pisaneschi, E, Marozza, A, Carli, D, Mussa, A, Radio, FC, Conti, B, Iascone, M, Gargano, G, Novelli, A, Tartaglia, M, Zuffardi, O, Bedeschi, MF and Garavelli, L.
Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome
Genes . 14(3): . Nº de cites: 12
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Costantino A, Campuzano O, Vaiano F, Nardi E, Dimitrova A, Greco A, Martínez-Barrios E, Arena V, Jarvis H, Sarquella-Brugada G, Brugada R, Oliva A and Grassi S.
Multidisciplinary and Personalized Molecular Diagnosis to Solving Sudden Death During Sport.
Molecular Diagnosis & Therapy . : .
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Perin F, Cartón AJ, Bermúdez-Jiménez FJ, Fernández-Barrio BC, Esmel-Vilomara R, Marcos-Fuentes L, Rueda Nuñez F, Rodríguez Vázquez Del Rey MDM, Montañés Delmás E, Ayerza-Casas A, Fernández-Tudela B, Viadero MT, Castro F, Siles A, Blanca-Jover E, Caravaca-Pantoja L, Bueno-Gómez A, Salamanca-Zarzuela B, De Vera McMullan P, López Blanco G, Plata-Izquierdo B, Jimenez Casso S, Serrano Robles MI, Matamala Morillo MÁ, Del Rey Megias L, Rocamora Salort S, Aparicio Fernández de Gatta C, Villares Alonso M, Arroyas Sánchez M, Ortega Montes A, Greco A, Martínez-Barrios E, Jiménez-Jáimez J, Roses-Noguer F and Sarquella-Brugada G.
Paediatric long QT syndrome: clinical outcomes and therapy in the Spanish National Registry.
EUROPEAN HEART JOURNAL . : .
