Publicaciones
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Olorón, PM, Alegría, I, César-Díaz S, del Olmo, B, Martínez-Barrios E, Carrera-García L, Natera-de Benito D, Nascimento-Osorio A, Campuzano, O and Sarquella-Brugada G.
Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 25(11): .
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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): .
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Pérez-Serra A, Toro R, Martínez-Barrios E, Iglesias A, Fernandez-Falgueras A, Alcalde M, Coll M, Puigmulé M, Del Olmo B, Picó F, Lopez L, Arbelo E, César-Díaz S, Llano CT, Mangas A, Brugada-Terradellas J, Sarquella-Brugada G, Brugada R and Campuzano O.
Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 25(7): . Nº de citas: 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 . 21(3): 331-339. Nº de citas: 1
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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): . Nº de citas: 2
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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: 3
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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: 6
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Nuria Díez Escuté, Arbelo E, Martínez-Barrios E, Patricia Cerralbo Martín, 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: 5
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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: 19