Browsing by author "Martín Fernández, María"

Evolución clínica de la enfermedad coronaria precoz. Prevención secundaria y bases genéticas

Martín Fernández, María

(2005-09-09)

Fibrilación auricular en el ictus criptogénico: ¿son necesarias nuevas herramientas para su diagnóstico?

Secades González, Sandra; Martín Fernández, María

; Hera Galarza, Jesús María de la

; Calleja Puerta, Sergio

(Elsevier, 2014)

Fisiopatología de la estenosis en la válvula aórtica bicúspide: estudio sobre tejido y análisis genético y de biomarcadores en sangre periférica

Junco Vicente, Alejandro (2024-04-12)

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier

Coto García, Eliecer

; Palacín Fernández, María

; Martín Fernández, María

; García Castro, Mónica

; Rodríguez Reguero, José Julián

; García Fernández, Cristina; Berrazueta Fernández, José Ramón de; Morís de la Tassa, César

; Morales Cañabete, Blanca

; Ortega Suárez, Francisco José

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Tavira Iglesias, Beatriz

; Álvarez Martínez, María Victoria

(2010)

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)

Rodríguez Reguero, José Julián

; Gómez de Oña, Juan

; Martín Fernández, María

; Flórez Muñoz, Juan Pablo; Morís de la Tassa, César

; Iglesias, Sara; Alonso González, Belén

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2013)

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Gómez de Oña, Juan

; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, José Julián

; Martín Fernández, María

; Morís de la Tassa, César

; Alonso González, Belén

; Iglesias, Sara; Díaz Molina, Beatriz

; Avanzas Fernández, Pablo

; Coto García, Eliecer

(2018)

A Giant Left Coronary Sinus of Valsalva Aneurysm After Type A Aortic Dissection

Martín Fernández, María

; Álvarez Cabo, Rubén; Barreiro Pérez, Manuel; Corros Vicente, Cecilia; García Campos, Ana; Rodríguez, María Luisa; Hera Galarza, Jesús María de la

; Hernández Luyando, Luis Isidoro

; Morís de la Tassa, César

(2014)

Heterotaxy syndrome = Síndrome de heterotaxia

Carro Hevia, Amelia

; Santamarta Liébana, Elena

; Martín Fernández, María

(2011)

Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?

Lorca Gutiérrez, Rebeca

; Martín Fernández, María

; Gómez de Oña, Juan

; Santamarta Liébana, Elena

; Morís de la Tassa, César

; Rodríguez Reguero, José Julián

; Coto García, Eliecer

(2015)

Il6 gene polymorphism association with calcific aortic valve stenosis and influence on serum levels of interleukin-6

Junco Vicente, Alejandro; Solache Berrocal, Guillermo; Del Río García, Álvaro; Rolle Sonora, Valeria; Areces, Sheila; Morís de la Tassa, César

; Martín Fernández, María

; Rodríguez, Isabel (2022)

The importance of echocardiography in Transcatheter Aortic Valve Implantation: TAVI: A Multimodality Approach

Martín Fernández, María

; Hernández Luyando, Luis Isidoro

; Hera Galarza, Jesús María de la

; Corros Vicente, Cecilia; García Campos, Ana; Rodríguez, María Luisa; García Ruiz, José Manuel

; Valle, Raquel del; Avanzas Fernández, Pablo

; Morís de la Tassa, César

(2014)

Malposition of the pacemaker lead in the left ventricle

Benito Martín, Eva M.; Rubín López, José Manuel

; Corros Vicente, Cecilia; Hera Galarza, Jesús María de la

; Martín Fernández, María

(2013)

A mass in the right atrium: A diagnostic dilemma

Colunga Blanco, Santiago; Martín Fernández, María

; Corros Vicente, Cecilia; Álvarez Cabo, Rubén; Astudillo González, María Aurora

(Elsevier Doyma, 2016)

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

Palacín Fernández, María

; Álvarez Martínez, María Victoria

; Martín Fernández, María

; Díaz González, Marta Elvira

; Corao Trueba, Ana Isabel

; Alonso González, Belén

; Díaz Molina, Beatriz

; Lozano Martínez-Luengas, Íñigo

; Avanzas Fernández, Pablo

; Morís de la Tassa, César

; Rodríguez Reguero, José Julián

; Rodríguez Fernández, Isabel

; López Larrea, Carlos

; Cannata Andía, Jorge Benito

; Batalla, Alberto; Ruiz Ortega, Marta; Martínez Camblor, Pablo

; Coto García, Eliecer

(2011)

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing

Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Martín Fernández, María

; Álvarez Martínez, María Victoria

; Alonso, Belén; Iglesias, Sara; Coto García, Eliecer

(2014)

Myopericarditis in a patient with ulcerative colitis treated with mesalazine

Martín Fernández, María

; Santamarta Liébana, Elena

; Marrugat de la Iglesia, Jaume; Saiz Ayala, Antonio

(2010)

Non compaction cardiomyopathy: A short review of a controversial entity

Lorca Gutiérrez, Rebeca

; Rozado Castaño, José; Martín Fernández, María

(2018)

Percutaneous femoral closure following thoracic aorta Stent graft placement: Preliminary results and 6 month follow up

Avanzas Fernández, Pablo

; Martín Fernández, María

; Lozano Martínez-Luengas, Alfonso Gerónimo

; Llaneza Coto, José Manuel

; Vega García, Florentino

; Fernández Suárez, Félix Ezequiel

; Hera Galarza, Jesús María de la

; Vegas Valle, José Miguel

; Rondán Murillo, Juan José

; Camacho Jiménez, José Benjamín; Valle Castro, José María; Morís de la Tassa, César

(2008)

Pre-participation screening and athlete's heart: A long way to run

Martín Fernández, María

; Lorca Gutiérrez, Rebeca

; Fernández García, Benjamín

; Rodríguez Reguero, José Julián

(2015)

The Prevalence of Patient-Prosthesis Mismatch Can Be Reduced Using the Trifecta Aortic Prosthesis

Hernández-Vaquero Panizo, Daniel

; Díaz, Rocío; Pascual Calleja, Isaac

; Rozado, J.; Hera Galarza, Jesús María de la

; León, Víctor; Avanzas Fernández, Pablo

; Martín Fernández, María

; García Iglesias, Daniel; Calvo Cuervo, David; Silva Guisasola, Jacobo Alberto

; Morís de la Tassa, César

(2018)

Browsing by author "Martín Fernández, María"

Evolución clínica de la enfermedad coronaria precoz. Prevención secundaria y bases genéticas ﻿

Fibrilación auricular en el ictus criptogénico: ¿son necesarias nuevas herramientas para su diagnóstico? ﻿

Fisiopatología de la estenosis en la válvula aórtica bicúspide: estudio sobre tejido y análisis genético y de biomarcadores en sangre periférica ﻿

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier ﻿

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain) ﻿

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy ﻿

A Giant Left Coronary Sinus of Valsalva Aneurysm After Type A Aortic Dissection ﻿

Heterotaxy syndrome = Síndrome de heterotaxia ﻿

Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum? ﻿

Il6 gene polymorphism association with calcific aortic valve stenosis and influence on serum levels of interleukin-6 ﻿

The importance of echocardiography in Transcatheter Aortic Valve Implantation: TAVI: A Multimodality Approach ﻿

Malposition of the pacemaker lead in the left ventricle ﻿

A mass in the right atrium: A diagnostic dilemma ﻿

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H ﻿

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing ﻿

Myopericarditis in a patient with ulcerative colitis treated with mesalazine ﻿

Non compaction cardiomyopathy: A short review of a controversial entity ﻿

Percutaneous femoral closure following thoracic aorta Stent graft placement: Preliminary results and 6 month follow up ﻿

Pre-participation screening and athlete's heart: A long way to run ﻿

The Prevalence of Patient-Prosthesis Mismatch Can Be Reduced Using the Trifecta Aortic Prosthesis ﻿

Evolución clínica de la enfermedad coronaria precoz. Prevención secundaria y bases genéticas

Fibrilación auricular en el ictus criptogénico: ¿son necesarias nuevas herramientas para su diagnóstico?

Fisiopatología de la estenosis en la válvula aórtica bicúspide: estudio sobre tejido y análisis genético y de biomarcadores en sangre periférica

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

A Giant Left Coronary Sinus of Valsalva Aneurysm After Type A Aortic Dissection

Heterotaxy syndrome = Síndrome de heterotaxia

Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?

Il6 gene polymorphism association with calcific aortic valve stenosis and influence on serum levels of interleukin-6

The importance of echocardiography in Transcatheter Aortic Valve Implantation: TAVI: A Multimodality Approach

Malposition of the pacemaker lead in the left ventricle

A mass in the right atrium: A diagnostic dilemma

Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: Evidence for an association to haplogroup H

Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor Next-Generation sequencing

Myopericarditis in a patient with ulcerative colitis treated with mesalazine

Non compaction cardiomyopathy: A short review of a controversial entity

Percutaneous femoral closure following thoracic aorta Stent graft placement: Preliminary results and 6 month follow up

Pre-participation screening and athlete's heart: A long way to run

The Prevalence of Patient-Prosthesis Mismatch Can Be Reduced Using the Trifecta Aortic Prosthesis