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OSCAR CAMPUZANO LARREA

Genètica Cardiovascular
Firma
OSCAR CAMPUZANO-LARREA
Posició
Investigador/a Consolidat - R3
Investigador/a Consolidat - R3
Projectes
Publicacions

Projectes

Genètica Cardiovascular

Ajuts per donar suport a les activitats dels grups de recerca de Catalunya (SGR-Cat 2021) - Genètica Cardiovascular (Gencardio)

Codi oficial: 2021 SGR 01611 Data inici: 01/01/2022 Data fi: 30/06/2025 Investigador/a principal: RAMON BRUGADA TERRADELLAS Organisme finançador: AGÈNCIA DE GESTIÓ UNIVERSITARIS I RECERCA

Publicacions

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
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
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
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
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
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
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
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
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-SAO PAULO, 2024, 22 dx.doi.org/10.31744/einstein_journal/2024AO0549
Sarquella-Brugada, G, Martinez-Barrios, E, Cesar, S, Toro, R, Cruzalegui, J, Greco, A, Diez-Escuté, N, Cerralbo, P, Chipa, F, Arbelo, E, Diez-López, C, Grazioli, G, Balderrábano, N, Campuzano, O

A narrative review of inherited arrhythmogenic syndromes in young population: role of genetic diagnosis in exercise recommendations

BMJ OPEN SPORT & EXERCISE MEDICINE, 2024, 10 dx.doi.org/10.1136/bmjsem-2023-001852

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