Lista de obras - Cristina Basso - Dominio Público Uruguay

A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life

artículo científico publicado en 2015

A novel kind of tumor type-characteristic junction: plakophilin-2 as a major protein of adherens junctions in cardiac myxomata

artículo científico publicado en 2010

Arrhythmogenic cardiomyopathy

artículo científico publicado en 2016

Arrhythmogenic right ventricular cardiomyopathy causing sudden cardiac death in boxer dogs: a new animal model of human disease

artículo científico publicado en 2004

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

artículo científico publicado en 2007

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2013

Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association For European Cardiovascular Pathology: II. Noninflammatory degenerative diseases - nomenclature and diagnostic criteria

artículo científico publicado en 2016

Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology: I. Inflammatory diseases

artículo científico publicado en 2015

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2013

Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

artículo científico publicado en 2012

Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro

artículo científico publicado en 2007

Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

artículo científico publicado en 2010

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2002

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2006

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2013

The ARVD/C genetic variants database: 2014 update

artículo científico publicado en 2015

Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement

artículo científico publicado en 2015

Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement

artículo científico publicado en 2015

Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies

artículo científico publicado en 2006

Lista de obras de Cristina Basso

A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life

A novel kind of tumor type-characteristic junction: plakophilin-2 as a major protein of adherens junctions in cardiac myxomata

Arrhythmogenic cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy causing sudden cardiac death in boxer dogs: a new animal model of human disease

Arrhythmogenic right ventricular cardiomyopathy/dysplasia

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy

Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association For European Cardiovascular Pathology: II. Noninflammatory degenerative diseases - nomenclature and diagnostic criteria

Consensus statement on surgical pathology of the aorta from the Society for Cardiovascular Pathology and the Association for European Cardiovascular Pathology: I. Inflammatory diseases

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy

Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro

Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy

The ARVD/C genetic variants database: 2014 update

Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement

Treatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statement

Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies