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out url icon Recercat 1 juny 2018 Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
out url icon Recercat 5 juny 2018 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
doc icon DUGiDocs 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
doc icon DUGiDocs 1 desembre 2016 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
out url icon Recercat 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
out url icon Recercat 1 juny 2018 Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology
out url icon Recercat 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
doc icon DUGiDocs novembre 2020 Impact of the COVID-19 lockdown on ischaemic heart disease: before-and-after observational study Avellana Rosales, Aina
doc icon DUGiDocs 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
doc icon DUGiDocs 2019 It is never too late for cardiac repair stem cell administration for chronic ischaemic heart infarction (SCACIHI) Escribano Pons, Miquel Àngel
doc icon DUGiDocs gener 2017 Long-term benefits of the cardiac rehabilitation programme in Girona: a three-year follow-up study Canal Garcia, Elena
out url icon Recercat Long-term benefits of the cardiac rehabilitation programme in Girona: a three-year follow-up study Canal Garcia, Elena
out url icon Recercat 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
out url icon Recercat 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
out url icon Recercat 1 juny 2018 A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome
out url icon Recercat 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
doc icon DUGiDocs 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
out url icon Recercat 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
out url icon Recercat 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
out url icon Recercat 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
out url icon Recercat 1 juny 2018 A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia
out url icon Recercat 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
out url icon Recercat 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
doc icon DUGiDocs 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
out url icon Recercat On the way to cure Atrial Fibrillation. Radiofrequency ablation vs cryoablation: Iatrogenic atrial septal defect after ablation procedures Soriano Hervás, Marta
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