|
|
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy |
Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Yotti, Raquel
; Espinosa, Maria Angeles
; PĂ©rez Serra, Alexandra
; Fernandez Avila, Ana Isabel
; Coll, Monica
; MĂ©ndez, Irene
; Iglesias, Anna
; Olmo, Bernat del
; RiurĂł CĂĄceres, Helena
; Cuenca, SofĂa
; Allegue, Catarina
; Campuzano Larrea, Oscar
; PicĂł, Ferran
; Ferrer Costa, Carles
; Ălvarez, Patricia
; Castillo, Sergio
; GarcĂa PavĂa, Pablo
; GonzĂĄlez LĂłpez, Esther
; Padron Barthe, Laura
; DĂaz de Bustamante, Aranzazu
; Darnaude, MarĂa Teresa
; Gonzålez Hevia, José Ignacio
; Brugada Terradellas, Josep
; Fernåndez Avilés, Francisco
; Brugada, Ramon
|
|
|
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy |
Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Yotti, Raquel
; Espinosa, Maria Angeles
; PĂ©rez Serra, Alexandra
; Fernandez Avila, Ana Isabel
; Coll, Monica
; MĂ©ndez, Irene
; Iglesias, Anna
; Olmo, Bernat del
; RiurĂł CĂĄceres, Helena
; Cuenca, SofĂa
; Allegue, Catarina
; Campuzano Larrea, Oscar
; PicĂł, Ferran
; Ferrer Costa, Carles
; Ălvarez, Patricia
; Castillo, Sergio
; GarcĂa PavĂa, Pablo
; GonzĂĄlez LĂłpez, Esther
; Padron Barthe, Laura
; DĂaz de Bustamante, Aranzazu
; Darnaude, MarĂa Teresa
; Gonzålez Hevia, José Ignacio
; Brugada Terradellas, Josep
; Fernåndez Avilés, Francisco
; Brugada, Ramon
|
|
2018 June 1 |
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy |
|
|
2018 June 5 |
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy |
Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Yotti, Raquel
; Espinosa, Maria Angeles
; PĂ©rez Serra, Alexandra
; Fernandez Avila, Ana Isabel
; Coll, Monica
; MĂ©ndez, Irene
; Iglesias, Anna
; Olmo, Bernat del
; RiurĂł CĂĄceres, Helena
; Cuenca, SofĂa
; Allegue, Catarina
; Campuzano Larrea, Oscar
; PicĂł, Ferran
; Ferrer Costa, Carles
; Ălvarez, Patricia
; Castillo, Sergio
; GarcĂa PavĂa, Pablo
; GonzĂĄlez LĂłpez, Esther
; Padron Barthe, Laura
; DĂaz de Bustamante, Aranzazu
; Darnaude, MarĂa Teresa
; Gonzålez Hevia, José Ignacio
; Brugada Terradellas, Josep
; Fernåndez Avilés, Francisco
; Brugada, Ramon
|
|
2017 August 3 |
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy |
Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Yotti, Raquel
; Espinosa, Maria Angeles
; Perez-Serra, Alexandra
; Fernandez Avila, Ana Isabel
; Coll Vidal, MĂČnica
; MĂ©ndez, Irene
; Iglesias, Anna
; Olmo, Bernat del
; RiurĂł CĂĄceres, Helena
; Cuenca, SofĂa
; Allegue Toscano, Catarina
; Campuzano Larrea, Oscar
; PicĂł, Ferran
; Ferrer Costa, Carles
; Ălvarez, Patricia
; Castillo, Sergio
; GarcĂa PavĂa, Pablo
; GonzĂĄlez LĂłpez, Esther
; Padron Barthe, Laura
; DĂaz de Bustamante, Aranzazu
; Darnaude, MarĂa Teresa
; Gonzålez Hevia, José Ignacio
; Brugada Terradellas, Josep
; Fernåndez Avilés, Francisco
; Brugada, Ramon
|
|
2018 June |
Characterization of non-coding genetic vairants associated with Brugada Syndrome: research and communication |
Torrecillas SanllehĂ, Anna
|
|
2015 |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort |
Selga Coma, Elisabet
; Campuzano Larrea, Oscar
; Pinsach Abuin, Mel·lina
; Perez-Serra, Alexandra
; Mademont Soler, Irene
; RiurĂł CĂĄceres, Helena
; PicĂł, Ferran
; Coll Vidal, MĂČnica
; Iglesias, Anna
; Pagans i Lista, Sara
; Sarquella Brugada, GeĂČrgia
; Berne, Paola
; Benito, Begoña
; Brugada Terradellas, Josep
; Porres, José M.
; LĂłpez Zea, Matilde
; Castro Urda, VĂctor
; FernĂĄndez Lozano, Ignacio
; Brugada, Ramon
|
|
|
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome |
Allegue, Catarina
; Coll, Monica
; MatĂ©s RamĂrez, JesĂșs
; 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
; MatĂ©s RamĂrez, JesĂșs
; 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, MĂČnica
; MatĂ©s RamĂrez, JesĂșs
; 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
; MatĂ©s RamĂrez, JesĂșs
; 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
; MatĂ©s RamĂrez, JesĂșs
; Iglesias, Anna
; Brugada Terradellas, Josep
; Brugada, Ramon
|
|
2022 |
La mort sobtada cardĂaca: buscant mutacions en els gens que codifiquen per als canals iĂČnics cardĂacs |
Bosch Masanas, Paula
|
|
|
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, Georgia
; Cesar, Sergi
; PĂ©rez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; 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
; PĂ©rez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; 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
; PĂ©rez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
|
2018 June 1 |
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
|
|
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
; PĂ©rez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
|
2020 February 15 |
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, GeĂČrgia
; Cesar, Sergi
; PĂ©rez Serra, Alexandra
; Coll, Monica
; Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|
|
2017 January 1 |
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia |
Bosch Calero, Cristina
; Campuzano Larrea, Oscar
; Sarquella Brugada, GeĂČrgia
; Cesar, Sergi
; Perez-Serra, Alexandra
; Coll Vidal, MĂČnica
; Mademont Soler, Irene
; MatĂ©s RamĂrez, JesĂșs
; Olmo, Bernat del
; Iglesias, Anna
; Brugada Terradellas, Josep
; Petersen, Volker
; Brugada, Ramon
|