OSCAR CAMPUZANO LARREA

Cardiovascular Genetics

Grassi, S, Vaiano, F, Dimitrova, A, Vullo, C, Croce, EB, Rossi, R, Arena, V, Rossi, SS, Campuzano, O, Brugada, R, Oliva, A

Fatal intoxications and inherited cardiac disorders in the young: where to draw the line?

INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2025, 139, 1081-1091 dx.doi.org/10.1007/s00414-025-03439-9

Cardiovascular Genetics

Ramos M, Enguita FJ, Bonet F, Ayala R, Gómez-Pavón FJ, Campuzano O, Toro R, Quezada-Feijoó M

MicroRNA-143-3p and miR-452-5p: A Fingerprint for the Diagnosis of Aortic Stenosis in the Geriatric Population.

Biomedicines, 2025, 13 dx.doi.org/10.3390/biomedicines13030671

Cardiovascular Genetics

Campuzano O, Sarquella-Brugada G, Toro R

MicroRNAs unlock the mystery of arrhythmogenic cardiomyopathy.

POLISH HEART JOURNAL-KARDIOLOGIA POLSKA, 2025, 83, 413-414 dx.doi.org/10.33963/v.phj.105101

Cardiovascular Genetics

Martínez-Barrios E, Greco A, Cesar S, Díez-López C, Cruzalegui J, Díez-Escuté N, Cerralbo P, Chipa F, Zschaeck I, Grassi S, Oliva A, Balderrábano N, Toro R, Sarquella-Brugada G, Campuzano O

Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes.

Iscience, 2025, 28, 112300-112300 dx.doi.org/10.1016/j.isci.2025.112300

Cardiovascular Genetics

Perez-Serra, A, Toro, R, Martinez-Barrios, E, Iglesias, A, Fernandez-Falgueras, A, Alcalde, M, Coll, M, Puigmule, M, del Olmo, B, Pico, F, Lopez, L, Arbelo, E, Cesar, S, Llano, CTD, Mangas, A, Brugada, J, Sarquella-Brugada, G, Brugada, R, Campuzano, O

Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 dx.doi.org/10.3390/ijms25073807

Cardiovascular Genetics

Campuzano, O, Sarquella-Brugada, G, Brugada, R

Sudden unexplained death in young people: A family matter

POLISH HEART JOURNAL-KARDIOLOGIA POLSKA, 2024, 82, 361-362 dx.doi.org/10.33963/v.phj.99975

Cardiovascular Genetics

Fernandez-Falgueras, A, Coll, M, Iglesias, A, Tiron, C, Campuzano, O, Brugada, R

The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe

Plos One, 2024, 19 dx.doi.org/10.1371/journal.pone.0297914

Cardiovascular Genetics

Fogaça-da-Mata, M, Martínez-Barrios, E, Jiménez-Montañés, L, Cruzalegui, J, Chipa-Ccasani, F, Greco, A, Cesar, S, Díez-Escuté, N, Cerralbo, P, Zschaeck, I, Adell, MC, Ayerza-Casas, A, Palanca-Arias, D, López, M, Campuzano, O, Brugada, J, Sarquella-Brugada, G

Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?

GENES, 2024, 15 dx.doi.org/10.3390/genes15050638

Cardiovascular Genetics

Olorón, PM, Alegría, I, Cesar, S, del Olmo, B, Martínez-Barrios, E, Carrera-García, L, Benito, DND, Nascimento, A, Campuzano, O, Sarquella-Brugada, G

Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 dx.doi.org/10.3390/ijms25115836

Cardiovascular Genetics

van der Steld LP, Rocha MS, Ladeia AMT, Livramento HL, Campos GB, Darrieux FCDC, Campuzano O, Brugada R

PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders.

EINSTEIN-SÃO PAULO, 2024, 22 dx.doi.org/10.31744/einstein_journal/2024AO0549

Directori

Publicacions

Fatal intoxications and inherited cardiac disorders in the young: where to draw the line?

MicroRNA-143-3p and miR-452-5p: A Fingerprint for the Diagnosis of Aortic Stenosis in the Geriatric Population.

MicroRNAs unlock the mystery of arrhythmogenic cardiomyopathy.

Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes.

Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy

Sudden unexplained death in young people: A family matter

The importance of variant reinterpretation in inherited cardiovascular diseases: Establishing the optimal timeframe

Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?

Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins

PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders.

Formulari de contacte

About IDIBGI!