OSCAR CAMPUZANO LARREA

Genètica Cardiovascular

Grassi S, Campuzano O, Ferri E, Leone G, Rossi R, Ortega-Sánchez M, Barberia E, Landin I, Arena V, Sarquella-Brugada G, Brugada R, Oliva A

Forensic pathological and genetic landmarks in sudden cardiac death in the young: An update.

FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2026, 80, 103334-103334 dx.doi.org/10.1016/j.fsigen.2025.103334

Genètica Cardiovascular

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

Genètica Cardiovascular

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

Genètica Cardiovascular

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

Genètica Cardiovascular

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

Genètica Cardiovascular

Coll M, Alcalde M, Fernández-Falgueras A, Iglesias A, Nogué-Navarro L, Tiron C, Campuzano O, Ortega M, Crespo S, Barberia E, Brugada R

Value of molecular autopsy in suspected sudden cardiac death in the young.

JOURNAL OF MOLECULAR DIAGNOSTICS, 2025, 27, 859-868 dx.doi.org/10.1016/j.jmoldx.2025.05.006

Genètica Cardiovascular

Campuzano O, Grassi S, Martínez-Barrios E, Greco A, Arena V, Sarquella-Brugada G, Oliva A

Brugada syndrome in the forensic field: what do we know to date?

Frontiers In Cardiovascular Medicine, 2025, 12, 1618762-1618762 dx.doi.org/10.3389/fcvm.2025.1618762

Genètica Cardiovascular

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

Genètica Cardiovascular

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

Genètica Cardiovascular

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

Directori

Publicacions

Forensic pathological and genetic landmarks in sudden cardiac death in the young: An update.

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.

Value of molecular autopsy in suspected sudden cardiac death in the young.

Brugada syndrome in the forensic field: what do we know to date?

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

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