Navegar por autor "Monserrat Iglesias, Lorenzo"

Genética, muerte súbita y deporte

2011- Monserrat Iglesias, Lorenzo; Barriales Villa, Roberto; Ortiz Genga, Martín

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

Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease

2020- Hu, D.; Hu, D.; Liu, L.; Barr, D.; Liu, Y.; [et al.]

Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic

2014- Monserrat Iglesias, Lorenzo

Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse

2011- Monserrat Iglesias, Lorenzo

Multidisciplinary approach to exercise-related sudden death families: a multicentric registry

2011- Monserrat Iglesias, Lorenzo

Mutations in left ventricular non compaction

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

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

2013- Monserrat Iglesias, Lorenzo

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

2015- Monserrat Iglesias, Lorenzo

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient

2013- Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso; Nuñez Fernandez, Lucia; Mosquera Perez, Ignacio; Rodriguez García, Isabel [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.]

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA)

2015- Monserrat Iglesias, Lorenzo

Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy

2012- Peteiro Vazquez, Jesus; Bouzas Mosquera, Alberto; Monserrat Iglesias, Lorenzo; Estevez Loureiro, Rodrigo; Castro Beiras, Alfonso; [et al.]

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

Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy

2013- Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso; Hermida Prieto, Manuel; Nuñez Fernandez, Lucia; Castro Nuñez, Lucia; [et al.]

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.]

O repositorio dixital RUNA

Navegar por autor "Monserrat Iglesias, Lorenzo"

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 ﻿

Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease ﻿

Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic ﻿

Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse ﻿

Multidisciplinary approach to exercise-related sudden death families: a multicentric registry ﻿

Mutations in left ventricular non compaction ﻿

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy ﻿

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy ﻿

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient ﻿

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

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA) ﻿

Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy ﻿

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

Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy ﻿

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 ﻿

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

Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease

Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic

Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse

Multidisciplinary approach to exercise-related sudden death families: a multicentric registry

Mutations in left ventricular non compaction

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient

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

Prediction of thrombo-embolic risk in patients with hypertrophic cardiomyopathy (HCM Risk-CVA)

Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy

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

Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy

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