Browse by Author "Barriales Villa, Roberto"

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy

2011- Monserrat Iglesias, Lorenzo; López, Begoña; González, Arantxa; Hermida Prieto, Manuel; Barriales Villa, Roberto; [et al.]

Clinical and functional consequences associated to a PKP2 founder mutation in north-west Spain

2011- Monserrat Iglesias, Lorenzo; Nuñez Fernandez, Lucia; García Estévez, Daniel Apolinar; Barriales Villa, Roberto; Ortiz Genga, Martín; [et al.]

Diagnóstico y tratamiento de la miocardiopatía hipertrófica: Comparación de las guías europeas y americanas

2015- Barriales Villa, Roberto

Genetics of cardiomyopathies: novel perspectives with next generation sequencing

2015- Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso; Barriales Villa, Roberto; Ortiz Genga, Martín; García Giustiniani, Daniel [et al.]

High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course

2015- Monserrat Iglesias, Lorenzo; Fernández Fernández, Xusto; Barriales Villa, Roberto; Ortiz Genga, Martín

Letter by Barriales-Villa et al Regarding Article,"Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies"

2019- Barriales Villa, Roberto; Larrañaga Moreira, José María; Ochoa ., Juan Pablo

Mutations in left ventricular non compaction

2011- Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso; Fernández Fernández, Xusto; Barriales Villa, Roberto; Cazón Varela, Laura [et al.]

Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker

2019- Lopez-Sainz, Angela; Climent, Vicente; Ripoll-Vera, Tomas; Espinosa, Maria Angeles; Barriales Villa, Roberto; [et al.]

Phenotype and prognostic correlations of the converter region mutations affecting the beta myosin heavy chain

2015- Monserrat Iglesias, Lorenzo; Barriales Villa, Roberto; Ortiz Genga, Martín; García Giustiniani, Daniel; Rodriguez García, Isabel [et al.]

Phenotype-genotype correlation in patients with mutations in the beta-myosin converter domain.

2012- Barriales Villa, Roberto; Ortiz Genga, Martín

Regional distribution of mutations associated with hypertrophic cardiomyopathy in the northwest of Spain

2011- Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso; Fernández Fernández, Xusto; Barriales Villa, Roberto

Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave

2014- Monserrat Iglesias, Lorenzo; Barriales Villa, Roberto; Ortiz Genga, Martín; García Giustiniani, Daniel

Varon de 17 años con hipertrofia ventricular izquierda: quien no sabe lo que busca, no entiende lo que encuentra

2011- Monserrat Iglesias, Lorenzo; Arévalo Gómez, Ana; Barriales Villa, Roberto; Rivera García, Susana; De la Cruz Alvarez, Jesús [et al.]

Yield of genetic testing in patients with familial vs. non-familial idiopathic dilated cardiomyopathy

2011- Monserrat Iglesias, Lorenzo; Crespo Leiro, Marisa; Castro Beiras, Alfonso; Barriales Villa, Roberto; Ortiz Genga, Martín; [et al.]

RUNA digital repository

Browse by Author "Barriales Villa, Roberto"

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy ﻿

Clinical and functional consequences associated to a PKP2 founder mutation in north-west Spain ﻿

Diagnóstico y tratamiento de la miocardiopatía hipertrófica: Comparación de las guías europeas y americanas ﻿

Fabry disease: A new mutation with phenotypic correlation? ﻿

Genética del síndrome de Marfan ﻿

Genética, muerte súbita y deporte ﻿

Genetics of cardiomyopathies: novel perspectives with next generation sequencing ﻿

High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course ﻿

Letter by Barriales-Villa et al Regarding Article,"Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies" ﻿

Mutations in left ventricular non compaction ﻿

Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker ﻿

Phenotype and prognostic correlations of the converter region mutations affecting the beta myosin heavy chain ﻿

Phenotype-genotype correlation in patients with mutations in the beta-myosin converter domain. ﻿

Regional distribution of mutations associated with hypertrophic cardiomyopathy in the northwest of Spain ﻿

Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave ﻿

Varon de 17 años con hipertrofia ventricular izquierda: quien no sabe lo que busca, no entiende lo que encuentra ﻿

Yield of genetic testing in patients with familial vs. non-familial idiopathic dilated cardiomyopathy ﻿

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy

Clinical and functional consequences associated to a PKP2 founder mutation in north-west Spain

Diagnóstico y tratamiento de la miocardiopatía hipertrófica: Comparación de las guías europeas y americanas

Fabry disease: A new mutation with phenotypic correlation?

Genética del síndrome de Marfan

Genética, muerte súbita y deporte

Genetics of cardiomyopathies: novel perspectives with next generation sequencing

High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course

Letter by Barriales-Villa et al Regarding Article,"Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies"

Mutations in left ventricular non compaction

Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker

Phenotype and prognostic correlations of the converter region mutations affecting the beta myosin heavy chain

Phenotype-genotype correlation in patients with mutations in the beta-myosin converter domain.

Regional distribution of mutations associated with hypertrophic cardiomyopathy in the northwest of Spain

Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave

Varon de 17 años con hipertrofia ventricular izquierda: quien no sabe lo que busca, no entiende lo que encuentra

Yield of genetic testing in patients with familial vs. non-familial idiopathic dilated cardiomyopathy