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Now showing items 1-14 of 14

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

2017-12-27 Article

Coll, Monica Pérez-Serra, Alexandra Matés Ramírez, Jesús Olmo, Bernat del et al.

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy

2017-08-03 Article

Mademont Soler, Irene Matés Ramírez, Jesús Yotti, Raquel Espinosa, Maria Angeles et al.

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia

2017-01-01 Article

Bosch Calero, Cristina Campuzano Larrea, Oscar Sarquella Brugada, Geòrgia Cesar, Sergi et al.

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

2016-12-08 Article

Sánchez Molero, Olallo Campuzano Larrea, Oscar Fernández Falgueras, Anna Sarquella Brugada, Geòrgia et al.

Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene

2016-07-08 Article

Toro, Rocio Pérez Serra, Alexandra Campuzano Larrea, Oscar Moncayo Arlandi, Javier et al.

Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies

2015-01-22 Article

Campuzano Larrea, Oscar Allegue, Catarina Fernández Falgueras, Anna Iglesias, Anna et al.

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

2015 Article

Allegue, Catarina Coll, Monica Matés Ramírez, Jesús Campuzano Larrea, Oscar et al.

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

2015 Article

Selga Coma, Elisabet Campuzano Larrea, Oscar Pinsach Abuin, Mel·lina Pérez Serra, Alexandra et al.

Rare titin (TTN) variants in diseases associated with sudden cardiac death

2015-01-01 Article

Campuzano Larrea, Oscar Sánchez Molero, Olallo Mademont Soler, Irene Riuró Cáceres, Helena et al.

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

2015 Article

Wangüemert, Fernando Bosch Calero, Cristina Pérez, Carmelo Campuzano Larrea, Oscar et al.

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

2014 Article

Alcalde Masegu, Mireia Campuzano Larrea, Oscar Berne, Paola García Pavía, Pablo et al.

Post-mortem genetic analysis in juvenile cases of sudden cardiac death

2014 Article

Campuzano Larrea, Oscar Sánchez Molero, Olallo Allegue, Catarina Coll, Monica et al.

The Role of clinical, genetic and segregation evaluation in sudden infant death

2014 Article

Campuzano Larrea, Oscar Allegue, Catarina Sarquella Brugada, Geòrgia Coll, Monica et al.

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

2013-01 Article

Tarradas Pou, Anna Selga Coma, Elisabet Beltrán Álvarez, Pedro Pérez Serra, Alexandra et al.

Now showing items 1-14 of 14

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Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene

Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

Rare titin (TTN) variants in diseases associated with sudden cardiac death

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

Post-mortem genetic analysis in juvenile cases of sudden cardiac death

The Role of clinical, genetic and segregation evaluation in sudden infant death

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome