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FormatDateTitleAuthor
FormatDateTitleAuthor
out url icon Recercat 2018 June 1 Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
out url icon Recercat 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 ; Mat√©s Ram√≠rez, Jes√ļs ; 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, M√≤nica ; Mat√©s Ram√≠rez, Jes√ļs ; Campuzano Larrea, Oscar ; Iglesias, Anna ; Sobrino, Beatriz ; Brion, Maria ; Amigo, Jorge ; Carracedo, Angel ; Brugada Terradellas, Pedro ; Brugada Terradellas, Josep ; Brugada, Ramon
doc icon DUGiDocs 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
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 ; Mat√©s Ram√≠rez, Jes√ļs ; Iglesias, Anna ; Brugada Terradellas, Josep ; Brugada, Ramon
out url icon Recercat 2018 June 1 Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology
out url icon Recercat 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 ; Mat√©s Ram√≠rez, Jes√ļs ; Iglesias, Anna ; Brugada Terradellas, Josep ; Brugada, Ramon
doc icon DUGiDocs 2020 November Impact of the COVID-19 lockdown on ischaemic heart disease: before-and-after observational study Avellana Rosales, Aina
doc icon DUGiDocs 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
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 2017 January 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
doc icon DUGiDocs 2022 La mort sobtada cardíaca: buscant mutacions en els gens que codifiquen per als canals iònics cardíacs Bosch Masanas, Paula
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 ; Beltr√°n √Ālvarez, Pedro ; P√©rez Serra, Alexandra ; Riur√≥ C√°ceres, Helena ; Pic√≥, Ferran ; Iglesias, Anna ; Campuzano Larrea, Oscar ; Castro Urda, V√≠ctor ; Fern√°ndez Lozano, Ignacio ; P√©rez Gonz√°lez, 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 ; Beltr√°n √Ālvarez, Pedro ; P√©rez Serra, Alexandra ; Riur√≥ C√°ceres, Helena ; Pic√≥, Ferran ; Iglesias, Anna ; Campuzano Larrea, Oscar ; Castro Urda, V√≠ctor ; Fern√°ndez Lozano, Ignacio ; P√©rez Gonz√°lez, Guillermo J. ; Scornik, Fabiana S. ; Brugada, Ramon
out url icon Recercat 2018 June 1 A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome
out url icon Recercat 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 ; Beltr√°n √Ālvarez, Pedro ; P√©rez Serra, Alexandra ; Riur√≥ C√°ceres, Helena ; Pic√≥, Ferran ; Iglesias, Anna ; Campuzano Larrea, Oscar ; Castro Urda, V√≠ctor ; Fern√°ndez Lozano, Ignacio ; P√©rez Gonz√°lez, Guillermo J. ; Scornik, Fabiana S. ; Brugada, Ramon
doc icon DUGiDocs 2013 January A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome Tarradas Pou, Anna ; Selga Coma, Elisabet ; Beltr√°n √Ālvarez, Pedro ; Perez-Serra, Alexandra ; Riur√≥ C√°ceres, Helena ; Pic√≥, Ferran ; Iglesias, Anna ; Campuzano Larrea, Oscar ; Castro Urda, V√≠ctor ; Fern√°ndez Lozano, Ignacio ; P√©rez Gonz√°lez, 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 ; P√©rez Serra, Alexandra ; Coll, Monica ; Mademont Soler, Irene ; Mat√©s Ram√≠rez, Jes√ļs ; 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 ; P√©rez Serra, Alexandra ; Coll, Monica ; Mademont Soler, Irene ; Mat√©s Ram√≠rez, Jes√ļs ; 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 ; P√©rez Serra, Alexandra ; Coll, Monica ; Mademont Soler, Irene ; Mat√©s Ram√≠rez, Jes√ļs ; Olmo, Bernat del ; Iglesias, Anna ; Brugada Terradellas, Josep ; Petersen, Volker ; Brugada, Ramon
out url icon Recercat 2018 June 1 A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia
out url icon Recercat 2018 June 5 A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia Bosch Calero, Cristina ; Campuzano Larrea, Oscar ; Sarquella Brugada, Georgia ; Cesar, Sergi ; P√©rez Serra, Alexandra ; Coll, Monica ; Mademont Soler, Irene ; Mat√©s Ram√≠rez, Jes√ļs ; Olmo, Bernat del ; Iglesias, Anna ; Brugada Terradellas, Josep ; Petersen, Volker ; Brugada, Ramon
out url icon Recercat 2020 February 15 A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia Bosch Calero, Cristina ; Campuzano Larrea, Oscar ; Sarquella Brugada, Ge√≤rgia ; Cesar, Sergi ; P√©rez Serra, Alexandra ; Coll, Monica ; Mademont Soler, Irene ; Mat√©s Ram√≠rez, Jes√ļs ; Olmo, Bernat del ; Iglesias, Anna ; Brugada Terradellas, Josep ; Petersen, Volker ; Brugada, Ramon
doc icon DUGiDocs 2017 January 1 A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia Bosch Calero, Cristina ; Campuzano Larrea, Oscar ; Sarquella Brugada, Ge√≤rgia ; Cesar, Sergi ; Perez-Serra, Alexandra ; Coll Vidal, M√≤nica ; Mademont Soler, Irene ; Mat√©s Ram√≠rez, Jes√ļs ; Olmo, Bernat del ; Iglesias, Anna ; Brugada Terradellas, Josep ; Petersen, Volker ; Brugada, Ramon
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