Genetic basis of atrial fibrillation

por Campuzano, Oscar, Perez-Serra, Alexandra, Iglesias, Anna, Brugada, Ramon
Publicado 2016

Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene

por Toro, Rocio, Pérez-Serra, Alexandra, Campuzano, Oscar, Moncayo-Arlandi, Javier, Allegue, Catarina, Iglesias, Anna, Mangas, Alipio, Brugada, Ramon
Publicado 2016

Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation

por Campuzano, Oscar, Sarquella-Brugada, Georgia, Arbelo, Elena, Cesar, Sergi, Jordà, Paloma, Pérez-Serra, Alexandra, Toro, Rocío, Brugada, Josep, Brugada, Ramon
Publicado 2020

Molecular heterogeneity of large-conductance calcium-activated potassium channels in canine intracardiac ganglia

por Selga, Elisabet, Pérez-Serra, Alexandra, Moreno-Asso, Alba, Anderson, Seth, Thomas, Kristen, Desai, Mayurika, Brugada, Ramon, Pérez, Guillermo J, Scornik, Fabiana S
Publicado 2013

Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family

por de Paula van der Steld, Lenises, Campuzano, Oscar, Pérez-Serra, Alexandra, de Barros Zamorano, Mabel Moura, Matos, Selma Sousa, Brugada, Ramon
Publicado 2017

Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death

por Campuzano, Oscar, Sanchez-Molero, Olallo, Mademont-Soler, Irene, Riuró, Helena, Allegue, Catarina, Coll, Monica, Pérez-Serra, Alexandra, Mates, Jesus, Picó, Ferran, Iglesias, Anna, Brugada, Ramon
Publicado 2015

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

por Coll, Monica, Pérez-Serra, Alexandra, Mates, Jesus, del Olmo, Bernat, Puigmulé, Marta, Fernandez-Falgueras, Anna, Iglesias, Anna, Picó, Ferran, Lopez, Laura, Brugada, Ramon, Campuzano, Oscar
Publicado 2017

A microRNA Signature for the Diagnosis of Statins Intolerance

por Mangas, Alipio, Pérez-Serra, Alexandra, Bonet, Fernando, Muñiz, Ovidio, Fuentes, Francisco, Gonzalez-Estrada, Aurora, Campuzano, Oscar, Rodriguez Roca, Juan Sebastian, Alonso-Villa, Elena, Toro, Rocio
Publicado 2022

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP

por Coll, Monica, Striano, Pasquale, Ferrer-Costa, Carles, Campuzano, Oscar, Matés, Jesús, del Olmo, Bernat, Iglesias, Anna, Pérez-Serra, Alexandra, Mademont, Irene, Picó, Ferran, Oliva, Antonio, Brugada, Ramon
Publicado 2017

miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury

por Toro, Rocío, Pérez-Serra, Alexandra, Mangas, Alipio, Campuzano, Oscar, Sarquella-Brugada, Georgia, Quezada-Feijoo, Maribel, Ramos, Mónica, Alcalá, Martin, Carrera, Esther, García-Padilla, Carlos, Franco, Diego, Bonet, Fernando
Publicado 2022

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

por Tarradas, Anna, Selga, Elisabet, Beltran-Alvarez, Pedro, Pérez-Serra, Alexandra, Riuró, Helena, Picó, Ferran, Iglesias, Anna, Campuzano, Oscar, Castro-Urda, Víctor, Fernández-Lozano, Ignacio, Pérez, Guillermo J., Scornik, Fabiana S., Brugada, Ramon
Publicado 2013

Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

por Jordà, Paloma, Toro, Rocío, Diez, Carles, Salazar-Mendiguchía, Joel, Fernandez-Falgueras, Anna, Perez-Serra, Alexandra, Coll, Monica, Puigmulé, Marta, Arbelo, Elena, García-Álvarez, Ana, Sarquella-Brugada, Georgia, Cesar, Sergi, Tiron, Coloma, Iglesias, Anna, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar
Publicado 2021

Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples

por Coll, Monica, Fernandez-Falgueras, Anna, Iglesias, Anna, del Olmo, Bernat, Nogue-Navarro, Laia, Simon, Adria, Perez Serra, Alexandra, Puigmule, Marta, Lopez, Laura, Pico, Ferran, Corona, Monica, Vallverdu-Prats, Marta, Tiron, Coloma, Campuzano, Oscar, Castella, Josep, Brugada, Ramon, Alcalde, Mireia
Publicado 2022

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants

por Campuzano, Oscar, Fernandez-Falgueras, Anna, Lemus, Ximena, Sarquella-Brugada, Georgia, Cesar, Sergi, Coll, Monica, Mates, Jesus, Arbelo, Elena, Jordà, Paloma, Perez-Serra, Alexandra, del Olmo, Bernat, Ferrer-Costa, Carles, Iglesias, Anna, Fiol, Victoria, Puigmulé, Marta, Lopez, Laura, Pico, Ferran, Brugada, Josep, Brugada, Ramon
Publicado 2019

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

por Selga, Elisabet, Campuzano, Oscar, Pinsach-Abuin, Mel·lina, Pérez-Serra, Alexandra, Mademont-Soler, Irene, Riuró, Helena, Picó, Ferran, Coll, Mònica, Iglesias, Anna, Pagans, Sara, Sarquella-Brugada, Georgia, Berne, Paola, Benito, Begoña, Brugada, Josep, Porres, José M., López Zea, Matilde, Castro-Urda, Víctor, Fernández-Lozano, Ignacio, Brugada, Ramon
Publicado 2015

Large Genomic Imbalances in Brugada Syndrome

por Mademont-Soler, Irene, Pinsach-Abuin, Mel·lina, Riuró, Helena, Mates, Jesus, Pérez-Serra, Alexandra, Coll, Mònica, Porres, José Manuel, del Olmo, Bernat, Iglesias, Anna, Selga, Elisabet, Picó, Ferran, Pagans, Sara, Ferrer-Costa, Carles, Sarquella-Brugada, Geòrgia, Arbelo, Elena, Cesar, Sergi, Brugada, Josep, Campuzano, Óscar, Brugada, Ramon
Publicado 2016

Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review

por Oliva, Antonio, Grassi, Simone, Pinchi, Vilma, Cazzato, Francesca, Coll, Mónica, Alcalde, Mireia, Vallverdú-Prats, Marta, Perez-Serra, Alexandra, Martínez-Barrios, Estefanía, Cesar, Sergi, Iglesias, Anna, Cruzalegui, José, Hernández, Clara, Fiol, Victoria, Arbelo, Elena, Díez-Escuté, Nuria, Arena, Vincenzo, Brugada, Josep, Sarquella-Brugada, Georgia, Brugada, Ramon, Campuzano, Oscar
Publicado 2022

Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies

por Campuzano, Oscar, Fernandez-Falgueras, Anna, Sarquella-Brugada, Georgia, Cesar, Sergi, Arbelo, Elena, García-Álvarez, Ana, Jordà, Paloma, Coll, Monica, Fiol, Victoria, Iglesias, Anna, Perez-Serra, Alexandra, Mates, Jesus, del Olmo, Bernat, Ferrer, Carles, Alcalde, Mireia, Puigmulé, Marta, Mademont-Soler, Irene, Pico, Ferran, Lopez, Laura, Tiron, Coloma, Brugada, Josep, Brugada, Ramon
Publicado 2019

Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes

por Martínez-Barrios, Estefanía, Sarquella-Brugada, Georgia, Pérez-Serra, Alexandra, Fernández-Falgueras, Anna, Cesar, Sergi, Coll, Mónica, Puigmulé, Marta, Iglesias, Anna, Alcalde, Mireia, Vallverdú-Prats, Marta, Ferrer-Costa, Carles, del Olmo, Bernat, Picó, Ferran, López, Laura, Fiol, Victoria, Cruzalegui, José, Hernández, Clara, Arbelo, Elena, Grassi, Simone, Oliva, Antonio, Toro, Rocío, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar
Publicado 2022

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

por Sanchez, Olallo, Campuzano, Oscar, Fernández-Falgueras, Anna, Sarquella-Brugada, Georgia, Cesar, Sergi, Mademont, Irene, Mates, Jesus, Pérez-Serra, Alexandra, Coll, Monica, Pico, Ferran, Iglesias, Anna, Tirón, Coloma, Allegue, Catarina, Carro, Esther, Gallego, María Ángeles, Ferrer-Costa, Carles, Hospital, Anna, Bardalet, Narcís, Borondo, Juan Carlos, Vingut, Albert, Arbelo, Elena, Brugada, Josep, Castellà, Josep, Medallo, Jordi, Brugada, Ramon
Publicado 2016