Publicaciones
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Cutler MJ, Eckhardt LL, Kaufman ES, Arbelo E, Behr ER, Brugada P, Cerrone M, Crotti L, DeAsmundis C, Gollob MH, Horie M, Huang DT, Krahn AD, London B, Lubitz SA, Mackall JA, Nademanee K, Perez MV, Probst V, Roden DM, Sacher F, Sarquella-Brugada G, Scheinman MM, Shimizu W, Shoemaker B, Sy RW, Watanabe A and Wilde AAM.
Clinical Management of Brugada Syndrome: Commentary From the Experts
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY . 17(1): .
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Martínez-Moreno R, Carreras D, Sarquella-Brugada G, Pérez GJ, Selga E, Scornik FS and Brugada R.
Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic background.
Heart Rhythm . : .
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Grassi S, Campuzano O, Cazzato F, Coll M, Puggioni A, Zedda M, Arena V, Iglesias A, Sarquella-Brugada G, Pinchi V, Brugada R and Oliva A.
Postmortem diagnosis of Takotsubo syndrome on autoptic findings: is it reliable? A systematic review
CARDIOVASCULAR PATHOLOGY . 65: 107543-107543. Nº de citas: 2
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Alcalde M, Toro R, Bonet F, Córdoba-Caballero J, Martínez-Barrios E, Ranea JA, Vallverdú-Prats M, Brugada R, Meraviglia V, Bellin M, Sarquella-Brugada G and Campuzano O.
Role of microRNAs in arrhythmogenic cardiomyopathy: translation as biomarkers into clinical practice
TRANSLATIONAL RESEARCH . 259: 72-82. Nº de citas: 1
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Kaski JP, Kammeraad JAE, Blom NA, Happonen JM, Janousek J, Klaassen S, Limongelli G, Östman-Smith I, Sarquella-Brugada G and Ziolkowska L.
Indications and management of implantable cardioverter-defibrillator therapy in childhood hypertrophic cardiomyopathy A position statement from the AEPC Working Group on Basic Science, Genetics and Myocardial Disease and the AEPC Working Group on Cardiac Dysrhythmias and Electrophysiology
CARDIOLOGY IN THE YOUNG . 33(5): 681-698. Nº de citas: 3
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Díez-Escuté N, Arbelo E, Martínez-Barrios E, Cerralbo P, César-Díaz S, Cruzalegui JC, Chipa F, Fiol JV, Zschaeck-Luzardo I, Hernández-Cera C, Campuzano O and Sarquella-Brugada G.
Sex differences in long QT syndrome
frontiers in cardiovascular medicine . 10: 1164028-1164028. Nº de citas: 2
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Landstrom, AA, Chahal, AJ, Ackerman, M, Cresci, SM, Milewicz, DA, Morris, A, Sarquella-Brugada G, Semsarian, CH, Shah, SC and Sturm, A.
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association
Circulation-Genomic and Precision Medicine . 16(2): . Nº de citas: 2
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César-Díaz S, Coll, M, Fiol JV, Fernandez-Falgueras, A, Cruzalegui JC, Iglesias, A, Moll I, Perez-Serra, A, Martínez-Barrios E, Ferrer-Costa, C, del Olmo, B, Puigmule, M, Alcalde, M, Lopez, L, Pico, F, Berrueco R, Brugada-Terradellas J, Zschaeck-Luzardo I, Natera-de Benito D, Carrera-García L, Exposito-Escudero JM, Ortez-Gonzalez CI, Nascimento-Osorio A, Brugada, R, Sarquella-Brugada G and Campuzano, O.
LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation
Frontiers in Genetics . 14: 1135438-1135438.
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César-Díaz S, Campuzano O, Cruzalegui JC, Fiol JV, Moll I, Martínez-Barrios E, Zschaeck-Luzardo I, Natera-de Benito D, Ortez-Gonzalez CI, Carrera-García L, Exposito-Escudero JM, Berrueco R, Bautista-Rodriguez C, Dabaj I, Gómez García-de-la-Banda M, Quijano-Roy S, Brugada-Terradellas J, Nascimento-Osorio A and Sarquella-Brugada G.
Characterization of cardiac involvement in children with LMNA-related muscular dystrophy
Frontiers in Cell and Developmental Biology . 11: 1142937-1142937. Nº de citas: 2
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Martínez-Barrios E, Grassi S, Brión M, Toro R, César-Díaz S, Cruzalegui JC, Coll M, Alcalde M, Brugada R, Greco A, Ortega-Sánchez ML, Barberia E, Oliva A, Sarquella-Brugada G and Campuzano O.
Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death
Frontiers in Medicine . 10: 1118585-1118585. Nº de citas: 4