|
2024 December |
Electrocardiografía a tu alcance |
Brugada, Ramon
; Singh, Manjot
|
|
|
2024 December |
Electrocardiography at your fingertips |
Brugada, Ramon
; Singh, Manjot
|
|
|
2017 February 1 |
Familial dilated cardiomyopathy: a multidisciplinary entity, from basic screening to novel circulating biomarkers |
de Gonzalo-Calvo D
; Quezada M
; Campuzano Larrea, Oscar
; Perez-Serra, Alexandra
; Broncano J
; Ayala R
; Ramos M
; Llorente-Cortes V
; Blasco-Turrión S
; Morales FJ
; Gonzalez P
; Brugada, Ramon
; Mangas A
; Toro R
|
|
|
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome |
Allegue, Catarina
; Coll, Monica
; Matés Ramírez, Jesús
; Campuzano Larrea, Oscar
; Iglesias, Anna
; Sobrino, Beatriz
; Brion, Maria
; Amigo, Jorge
; Carracedo, Angel
; Brugada Terradellas, Pedro
; Brugada Terradellas, Josep
; Brugada, Ramon
|
|
|
2018 June 1 |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome |
|
|
|
2018 June 5 |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome |
Allegue, Catarina
; Coll, Monica
; Matés Ramírez, Jesús
; Campuzano Larrea, Oscar
; Iglesias, Anna
; Sobrino, Beatriz
; Brion, Maria
; Amigo, Jorge
; Carracedo, Angel
; Brugada Terradellas, Pedro
; Brugada Terradellas, Josep
; Brugada, Ramon
|
|
|
2015 |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome |
Allegue Toscano, Catarina
; Coll Vidal, Mònica
; Matés Ramírez, Jesús
; Campuzano Larrea, Oscar
; Iglesias, Anna
; Sobrino, Beatriz
; Brion, Maria
; Amigo, Jorge
; Carracedo, Angel
; Brugada Terradellas, Pedro
; Brugada Terradellas, Josep
; Brugada, Ramon
|
|
|
2016 December 1 |
Genetic basis of dilated cardiomyopathy |
Perez-Serra, Alexandra
; Toro R
; Sarquella-Brugada G
; de Gonzalo-Calvo D
; Cesar S
; Carro E
; Llorente-Cortes V
; Iglesias A
; Brugada J
; Brugada, Ramon
; Campuzano Larrea, Oscar
|
|
|
|
Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology |
Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Mademont Soler, Irene
; Allegue, Catarina
; Cesar, Sergi
; Ferrer Costa, Carles
; Coll, Monica
; Matés Ramírez, Jesús
; Iglesias, Anna
; Brugada Terradellas, Josep
; Brugada, Ramon
|
|
|
2018 June 1 |
Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology |
|
|
|
2018 June 5 |
Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology |
Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Mademont Soler, Irene
; Allegue, Catarina
; Cesar, Sergi
; Ferrer Costa, Carles
; Coll, Monica
; Matés Ramírez, Jesús
; Iglesias, Anna
; Brugada Terradellas, Josep
; Brugada, Ramon
|
|
|
2020 November |
Impact of the COVID-19 lockdown on ischaemic heart disease: before-and-after observational study |
Avellana Rosales, Aina
|
|
|
2021 November |
The implementation of a cardiac rehabilitation program adapted to child’s requirements in paediatric population with congenital heart disease: a randomized, controlled, and open-label clinical trial |
Boadas Gironès, Mireia
|
|
|
2019 |
It is never too late for cardiac repair stem cell administration for chronic ischaemic heart infarction (SCACIHI) |
Escribano Pons, Miquel Àngel
|
|
|
2017 January |
Long-term benefits of the cardiac rehabilitation programme in Girona: a three-year follow-up study |
Canal Garcia, Elena
|
|
|
|
Long-term benefits of the cardiac rehabilitation programme in Girona: a three-year follow-up study |
Canal Garcia, Elena
|
|
|
2022 |
La mort sobtada cardíaca: buscant mutacions en els gens que codifiquen per als canals iònics cardíacs |
Bosch Masanas, Paula
|
|
|
|
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
Tarradas Pou, Anna
; Selga Coma, Elisabet
; Beltrán Álvarez, Pedro
; Pérez Serra, Alexandra
; Riuró Cáceres, Helena
; Picó, Ferran
; Iglesias, Anna
; Campuzano Larrea, Oscar
; Castro Urda, Víctor
; Fernández Lozano, Ignacio
; Pérez González, Guillermo J.
; Scornik, Fabiana S.
; Brugada, Ramon
|
|
|
|
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
Tarradas Pou, Anna
; Selga Coma, Elisabet
; Beltrán Álvarez, Pedro
; Pérez Serra, Alexandra
; Riuró Cáceres, Helena
; Picó, Ferran
; Iglesias, Anna
; Campuzano Larrea, Oscar
; Castro Urda, Víctor
; Fernández Lozano, Ignacio
; Pérez González, Guillermo J.
; Scornik, Fabiana S.
; Brugada, Ramon
|
|
|
2018 June 1 |
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
|
|
|
2018 June 5 |
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
Tarradas Pou, Anna
; Selga Coma, Elisabet
; Beltrán Álvarez, Pedro
; Pérez Serra, Alexandra
; Riuró Cáceres, Helena
; Picó, Ferran
; Iglesias, Anna
; Campuzano Larrea, Oscar
; Castro Urda, Víctor
; Fernández Lozano, Ignacio
; Pérez González, Guillermo J.
; Scornik, Fabiana S.
; Brugada, Ramon
|
|
|
2013 January |
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
Tarradas Pou, Anna
; Selga Coma, Elisabet
; Beltrán Álvarez, Pedro
; Perez-Serra, Alexandra
; Riuró Cáceres, Helena
; Picó, Ferran
; Iglesias, Anna
; Campuzano Larrea, Oscar
; Castro Urda, Víctor
; Fernández Lozano, Ignacio
; Pérez González, Guillermo J.
; Scornik, Fabiana S.
; Brugada, Ramon
|
|
|
|
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Cesar, Sergi
; Pérez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; Matés Ramírez, Jesús
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
|
|
|
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Cesar, Sergi
; Pérez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; Matés Ramírez, Jesús
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
|
|
|
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Cesar, Sergi
; Pérez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; Matés Ramírez, Jesús
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
