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Genetics of channelopathies associated with sudden cardiac death |
Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Brugada, Ramon
; Brugada Terradellas, Josep
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Genetics of channelopathies associated with sudden cardiac death |
Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Brugada, Ramon
; Brugada Terradellas, Josep
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1 juny 2018 |
Genetics of channelopathies associated with sudden cardiac death |
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5 juny 2018 |
Genetics of channelopathies associated with sudden cardiac death |
Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Brugada, Ramon
; Brugada Terradellas, Josep
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13 octubre 2015 |
Genetics of channelopathies associated with sudden cardiac death |
Campuzano Larrea, Oscar
; Sarquella Brugada, Geòrgia
; Brugada, Ramon
; Brugada Terradellas, Josep
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15 febrer 2020 |
Genetics of channelopathies associated with sudden cardiac death |
Campuzano Larrea, Oscar
; Sarquella Brugada, Geòrgia
; Brugada, Ramon
; Brugada Terradellas, Josep
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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
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1 juny 2018 |
Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology |
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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
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9 abril 2019 |
Influencia de la grasa epicárdica en la arritmia: fibrilación auricular, la cardioversión eléctrica, la recurrencia y el tratamiento |
Valenzuela Leal, Helen
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Large Genomic Imbalances in Brugada Syndrome |
Mademont Soler, Irene
; Pinsach Abuin, Mel·lina
; Riuró Cáceres, Helena
; Matés Ramírez, Jesús
; Pérez Serra, Alexandra
; Coll, Monica
; Porres, José M.
; Olmo, Bernat del
; Iglesias, Anna
; Selga Coma, Elisabet
; Picó, Ferran
; Pagans i Lista, Sara
; Ferrer Costa, Carles
; Sarquella Brugada, Georgia
; Arbelo, Elena
; Cesar, Sergi
; Brugada Terradellas, Josep
; Campuzano Larrea, Oscar
; Brugada, Ramon
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1 juny 2018 |
Large Genomic Imbalances in Brugada Syndrome |
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5 juny 2018 |
Large Genomic Imbalances in Brugada Syndrome |
Mademont Soler, Irene
; Pinsach Abuin, Mel·lina
; Riuró Cáceres, Helena
; Matés Ramírez, Jesús
; Pérez Serra, Alexandra
; Coll, Monica
; Porres, José M.
; Olmo, Bernat del
; Iglesias, Anna
; Selga Coma, Elisabet
; Picó, Ferran
; Pagans i Lista, Sara
; Ferrer Costa, Carles
; Sarquella Brugada, Georgia
; Arbelo, Elena
; Cesar, Sergi
; Brugada Terradellas, Josep
; Campuzano Larrea, Oscar
; Brugada, Ramon
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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
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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
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1 juny 2018 |
A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome |
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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
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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
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20 gener 2016 |
Paper de la placofilina-2 en la miocardiopatia aritmogènica de ventricle dret: bases genètiques i mecanismes moleculars |
Alcalde Masegu, Mireia
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Paper de la placofilina-2 en la miocardiopatia aritmogènica de ventricle dret: bases genètiques i mecanismes moleculars |
Alcalde Masegu, Mireia
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gener 2016 |
Prevalence of QTc alterations in neonates: age and genetic determinants: end of term project |
Teixidor Camps, Mariona
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Prevalence of QTc alterations in neonates: age and genetic determinants: end of term project |
Teixidor Camps, Mariona
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Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy |
Alcalde Masegu, Mireia
; Campuzano Larrea, Oscar
; Berne, Paola
; García Pavía, Pablo
; Doltra, Ada
; Arbelo, Elena
; Sarquella Brugada, Georgia
; Iglesias, Anna
; Alonso Pulpón, Luis
; Brugada Terradellas, Josep
; Brugada, Ramon
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Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy |
Alcalde Masegu, Mireia
; Campuzano Larrea, Oscar
; Berne, Paola
; García Pavía, Pablo
; Doltra, Ada
; Arbelo, Elena
; Sarquella Brugada, Georgia
; Iglesias, Anna
; Alonso Pulpón, Luis
; Brugada Terradellas, Josep
; Brugada, Ramon
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1 juny 2018 |
Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy |
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