|
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
|
|
|
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
|
|
1 juny 2018 |
Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology |
|
|
5 juny 2018 |
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
|
|
novembre 2021 |
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
|
|
gener 2017 |
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
|
|
1 juny 2018 |
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
|
|
5 juny 2018 |
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
|
|
gener 2013 |
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
|
|
1 juny 2018 |
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
|
|
5 juny 2018 |
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
|
|
15 febrer 2020 |
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, Geòrgia
; 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
|
|
1 gener 2017 |
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, Geòrgia
; Cesar, Sergi
; Perez-Serra, Alexandra
; Coll Vidal, Mònica
; Mademont Soler, Irene
; Matés Ramírez, Jesús
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
|
|
On the way to cure Atrial Fibrillation. Radiofrequency ablation vs cryoablation: Iatrogenic atrial septal defect after ablation procedures |
Soriano Hervás, Marta
|
|
gener 2015 |
On the way to cure Atrial Fibrillation. Radiofrequency ablation vs cryoablation: Iatrogenic atrial septal defect after ablation procedures |
Soriano Hervás, Marta
|
|
|
On the way to cure Atrial Fibrillation. Radiofrequency ablation vs cryoablation: Iatrogenic atrial septal defect after ablation procedures |
Soriano Hervás, Marta
|
|
|
Post-mortem genetic analysis in juvenile cases of sudden cardiac death |
Campuzano Larrea, Oscar
; Sánchez Molero, Olallo
; Allegue, Catarina
; Coll, Monica
; Mademont Soler, Irene
; Selga Coma, Elisabet
; Ferrer Costa, Carles
; Matés Ramírez, Jesús
; Iglesias, Anna
; Sarquella Brugada, Georgia
; Cesar, Sergi
; Brugada Terradellas, Josep
; Castellà, Josep
; Medallo, Jordi
; Brugada, Ramon
|
|
|
Post-mortem genetic analysis in juvenile cases of sudden cardiac death |
Campuzano Larrea, Oscar
; Sánchez Molero, Olallo
; Allegue, Catarina
; Coll, Monica
; Mademont Soler, Irene
; Selga Coma, Elisabet
; Ferrer Costa, Carles
; Matés Ramírez, Jesús
; Iglesias, Anna
; Sarquella Brugada, Georgia
; Cesar, Sergi
; Brugada Terradellas, Josep
; Castellà, Josep
; Medallo, Jordi
; Brugada, Ramon
|