Browsing by author "Lorca Gutiérrez, Rebeca"

Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome

Gómez de Oña, Juan

; Muñiz Albaiceta, Guillermo

; García Clemente, Marta María

; López Larrea, Carlos

; Amado Rodríguez, Laura

; López Alonso, Inés

; Hermida, T.; Enríquez Rodríguez, Ana Isabel; Herrero, P.; Melón García, Santiago

; Alvarez Argüelles, Marta Elena; Boga Riveiro, José Antonio; Rojo Alba, S.; Cuesta Llavona, Elías; Alvarez, V.; Lorca Gutiérrez, Rebeca

; Coto García, Eliecer

(2020)

Bicuspid aortic valve syndrome: a multidisciplinary approach for a complex entity

Martín Fernández, María

; Lorca Gutiérrez, Rebeca

; Rozado Castaño, José; Álvarez Cabo, Rubén; Calvo, Juan; Pascual Calleja, Isaac

; Cigarrán, H.; Rodríguez Fernández, Isabel

; Morís de la Tassa, César

(2017)

Bicuspid aortopathy: The show must go on

Martín Fernández, María

; Lorca Gutiérrez, Rebeca

; Morís de la Tassa, César

(2017)

Caracterización clínica y genotípica de patologías cardiovasculares familiares o de base genética

Salgado Barquinero, María (2024-12-03)

Characterization of left ventricular non-compaction cardiomyopathy

Lorca Gutiérrez, Rebeca

; Martín Fernández, María

; Pascual Calleja, Isaac

; Astudillo González, María Aurora

; Díaz Molina, Beatriz

; Cigarrán, Helena; Cuesta Llavona, Elías; Avanzas Fernández, Pablo

; Rodríguez Reguero, José Julián

; Coto García, Eliecer

; Morís de la Tassa, César

; Gómez de Oña, Juan

(2020)

Chromosome Y haplogroup R was associated with the risk of premature myocardial infarction with ST-elevation: data from the choleSTEMI registry

Lorca Gutiérrez, Rebeca

; Aparicio, A.; Salgado, M.; Álvarez Velasco, Rut; Pascual Calleja, Isaac

; Gómez, J.; Vázquez Coto, D.; García Lago, C.; Velázquez Cuervo, L.; Cuesta Llavona, Elías; Avanzas Fernández, Pablo

; Coto García, Eliecer

(2023)

Coexistencia de progresión transmural y lateral del frente de onda en el infarto de miocardio humano

Lorca Gutiérrez, Rebeca

; Jiménez Blanco, M.; García Ruiz, J. M. (2020)

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders

Lorca Gutiérrez, Rebeca

; Pannone, L.; Cuesta Llavona, Elías; Bocchinfuso, G.; Rodríguez Reguero, José Julián

; Carpentieri, G.; Hernando, Inés; Flex, E.; Tartaglia, M.; Coto García, Eliecer

; Gómez, Juan; Martinelli, S. (2021)

Concealed inherited cardiomyopathies detected in cardio-oncology screening

Lorca Gutiérrez, Rebeca

; Pascual Calleja, Isaac

; Fernández, M.; Álvarez Velasco, Rut; Colunga, Santiago; Muñiz, M.; Izquierdo, M.; Fernández, Y.; Esteban, E.; Gómez, Juan; Avanzas Fernández, Pablo

; López Fernández, Teresa (2024)

Correlación fenotipo/genotipo en la miocardiopatía hipertrófica y miocardiopatía no compactada

Lorca Gutiérrez, Rebeca

(2018-01-12)

Different phenotypes in monozygotic twins, carriers of the same pathogenic variant for hypertrophic cardiomyopathy

Rodríguez Junquera, Manuel; Salgado, María; González Urbistondo, Francisco; Alen, Alberto; Rodríguez Reguero, José Julián

; Silva, Iria; Coto García, Eliecer

; Avanzas Fernández, Pablo

; Morís de la Tassa, César

; Gómez de Oña, Juan

; Lorca Gutiérrez, Rebeca

(2022)

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora

Lorca Gutiérrez, Rebeca

; Gómez de Oña, Juan

; Martín, María; Cabanillas Farpón, Rubén

; Calvo Blanco, Juan

; León, Víctor; Pascual Calleja, Isaac

; Morís de la Tassa, César

; Coto García, Eliecer

; Rodríguez Reguero, José Julián

(2019)

Epigenetic study of cohort of monozygotic twins with hypertrophic cardiomyopathy due to MYBPC3 (Cardiac Myosin-Binding protein C)

Peñarroya, A.; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, Juan Ramón; Gómez, Juan; Avanzas Fernández, Pablo

; Tejedor Vaquero, Juan Ramón

; Fernández Fernández, Agustín

; Fernández Fraga, Mario

(2024)

Evaluación del perfil de riesgo cardiovascular, tratamiento y evolución clínica de pacientes jóvenes ingresados por síndrome coronario agudo.

Gutiérrez de la Varga, Luis (2024-06-03)

Evaluation of cardiovascular events in patients with hepatocellular carcinoma treated with sorafenib in the clinical practice. The Cardio-sor study

Carballo Folgoso, Lorena; Ávarez Velasco, Rut; Lorca Gutiérrez, Rebeca

; Castaño García, Andrés; Cuevas, Javier; Luisa González Diéguez, María Luisa; Martin, Maria; Álvarez Navascués, Carmen; Cadahía Rodrigo, Valle; Morís de la Tassa, César

; Rodríguez García, Manuel

; Varela Calvo, María

(2021)

Factores de riesgo cardiovascular e hipercolesterolemia familiar en cardiopatía isquémica precoz

Aparicio Gavilanes, Andrea (2023-06-27)

Fever, Malaise, and Dyspnea in a Diabetic Heart Transplant Patient: A Case Report

Alperi, Alberto; Pascual Calleja, Isaac

; Díaz Molina, Beatriz

; Silva Conde, Iria; Lorca Gutiérrez, Rebeca

; Hernández-Vaquero Panizo, Daniel

; Avanzas Fernández, Pablo

; Lambert Rodríguez, José Luis; Morís de la Tassa, César

(2017)

Frailty assessment in a cohort of elderly patients with severe symptomatic aortic stenosis: insights from the FRailty Evaluation in Severe Aortic Stenosis (FRESAS) registry

Solla Suárez, Pablo; Avanzas Fernández, Pablo

; Pascual Calleja, Isaac

; Bermúdez-Menéndez de la Granda, Manuel; Almendárez, M.; Arche Coto, José M.; Hernández Vaquero, Daniel

; Lorca Gutiérrez, Rebeca

; López Álvarez, Eva; Álvarez Velasco, Rut; Moreno Planillo, Carmen; Morís de la Tassa, César

; Gutiérrez Rodríguez, José (2021)

Functional mitral regurgitation: structural modifications with percutaneous valve repair with MitraClip

Alperi García, Alberto; Avanzas Fernández, Pablo

; Pascual Calleja, Isaac

; Adeba, Antonio; Lorca Gutiérrez, Rebeca

; León, Víctor; Almendárez, Marcel; Cubero Gallego, Héctor; Silva Conde, Iria; Morís de la Tassa, César

; Hernández-Vaquero Panizo, Daniel

(2020)

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)

Browsing by author "Lorca Gutiérrez, Rebeca"

Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome ﻿

Bicuspid aortic valve syndrome: a multidisciplinary approach for a complex entity ﻿

Bicuspid aortopathy: The show must go on ﻿

Caracterización clínica y genotípica de patologías cardiovasculares familiares o de base genética ﻿

Characterization of left ventricular non-compaction cardiomyopathy ﻿

Chromosome Y haplogroup R was associated with the risk of premature myocardial infarction with ST-elevation: data from the choleSTEMI registry ﻿

Coexistencia de progresión transmural y lateral del frente de onda en el infarto de miocardio humano ﻿

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders ﻿

Concealed inherited cardiomyopathies detected in cardio-oncology screening ﻿

Correlación fenotipo/genotipo en la miocardiopatía hipertrófica y miocardiopatía no compactada ﻿

Different phenotypes in monozygotic twins, carriers of the same pathogenic variant for hypertrophic cardiomyopathy ﻿

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora ﻿

Epigenetic study of cohort of monozygotic twins with hypertrophic cardiomyopathy due to MYBPC3 (Cardiac Myosin-Binding protein C) ﻿

Evaluación del perfil de riesgo cardiovascular, tratamiento y evolución clínica de pacientes jóvenes ingresados por síndrome coronario agudo. ﻿

Evaluation of cardiovascular events in patients with hepatocellular carcinoma treated with sorafenib in the clinical practice. The Cardio-sor study ﻿

Factores de riesgo cardiovascular e hipercolesterolemia familiar en cardiopatía isquémica precoz ﻿

Fever, Malaise, and Dyspnea in a Diabetic Heart Transplant Patient: A Case Report ﻿

Frailty assessment in a cohort of elderly patients with severe symptomatic aortic stenosis: insights from the FRailty Evaluation in Severe Aortic Stenosis (FRESAS) registry ﻿

Functional mitral regurgitation: structural modifications with percutaneous valve repair with MitraClip ﻿

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

Angiotensin-converting enzymes (ACE, ACE2) gene variants and COVID-19 outcome

Bicuspid aortic valve syndrome: a multidisciplinary approach for a complex entity

Bicuspid aortopathy: The show must go on

Caracterización clínica y genotípica de patologías cardiovasculares familiares o de base genética

Characterization of left ventricular non-compaction cardiomyopathy

Chromosome Y haplogroup R was associated with the risk of premature myocardial infarction with ST-elevation: data from the choleSTEMI registry

Coexistencia de progresión transmural y lateral del frente de onda en el infarto de miocardio humano

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders

Concealed inherited cardiomyopathies detected in cardio-oncology screening

Correlación fenotipo/genotipo en la miocardiopatía hipertrófica y miocardiopatía no compactada

Different phenotypes in monozygotic twins, carriers of the same pathogenic variant for hypertrophic cardiomyopathy

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora

Epigenetic study of cohort of monozygotic twins with hypertrophic cardiomyopathy due to MYBPC3 (Cardiac Myosin-Binding protein C)

Evaluación del perfil de riesgo cardiovascular, tratamiento y evolución clínica de pacientes jóvenes ingresados por síndrome coronario agudo.

Evaluation of cardiovascular events in patients with hepatocellular carcinoma treated with sorafenib in the clinical practice. The Cardio-sor study

Factores de riesgo cardiovascular e hipercolesterolemia familiar en cardiopatía isquémica precoz

Fever, Malaise, and Dyspnea in a Diabetic Heart Transplant Patient: A Case Report

Frailty assessment in a cohort of elderly patients with severe symptomatic aortic stenosis: insights from the FRailty Evaluation in Severe Aortic Stenosis (FRESAS) registry

Functional mitral regurgitation: structural modifications with percutaneous valve repair with MitraClip

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