Navegar por autor "Monserrat Iglesias, Lorenzo"

A family with recurrent sudden death and no clinical clue

2012- Monserrat Iglesias, Lorenzo

A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

2023- Cámara-Checa, A.; Perin, F.; Rubio-Alarcón, M.; Dago, M.; Crespo-García, T.; [et al.]

A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve

2023- Siguero-Álvarez, M.; Salguero-Jiménez, A.; Grego-Bessa, J.; de la Barrera, J.; MacGrogan, D.; [et al.]

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy

2015- Monserrat Iglesias, Lorenzo; Ortiz Genga, Martín

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD)

2014- Monserrat Iglesias, Lorenzo

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy: A proof of concept study

2012- Monserrat Iglesias, Lorenzo

A novel Troponin I mutation associated with severe restrictive cardiomyopathy - A case report of a 27-year-old woman with fatigue

2022- Gerhardt, T.; Monserrat Iglesias, Lorenzo; Landmesser, U.; Poller, W.

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

2023- Lopes, L.R.; Losi, M.-A.; Sheikh, N.; Laroche, C.; Charron, P.; [et al.]

Atlas of the clinical genetics of human dilated cardiomyopathy

2015- Monserrat Iglesias, Lorenzo; Crespo Leiro, Marisa; Ortiz Genga, Martín; García Giustiniani, Daniel

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.]

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype

2014- Monserrat Iglesias, Lorenzo; Ortiz Genga, Martín

Diagnostic approach of idiopathic ventricular fibrillation: results from the FIVI-Gen study

2014- Monserrat Iglesias, Lorenzo

Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study)

2015- Monserrat Iglesias, Lorenzo

Doppler tisular y estratificación del riesgo en la miocardiopatía hipertrófica

2014- Monserrat Iglesias, Lorenzo

Effects of Prolonged-Release Torasemide Versus Furosemide on Myocardial Fibrosis in Hypertensive Patients with Chronic Heart Failure: A Randomized, Blinded End Point, Active-Controlled Study

2011- González Juanatey, José Ramón; Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso

Enlarging the genetic spectrum of cardiomyopathies. Preliminary results of the myestela pediatric cohort study

2011- Monserrat Iglesias, Lorenzo

Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy

2015- Peteiro Vazquez, Jesus; Bouzas Mosquera, Alberto; Monserrat Iglesias, Lorenzo; Soler Fernandez, Rafaela; Castro Beiras, Alfonso; [et al.]

Fabry disease: A new mutation with phenotypic correlation?

2011- Monserrat Iglesias, Lorenzo; Arévalo Gómez, Ana; Barriales Villa, Roberto; Rivera García, Susana

Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin Gene

2020- Poller, Wolfgang; Haas, Jan; Klingel, Karin; Kühnisch, Jirko; Gast, Martina; [et al.]

O repositorio dixital RUNA

Navegar por autor "Monserrat Iglesias, Lorenzo"

A family with recurrent sudden death and no clinical clue ﻿

A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family ﻿

A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve ﻿

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy ﻿

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD) ﻿

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy: A proof of concept study ﻿

A novel Troponin I mutation associated with severe restrictive cardiomyopathy - A case report of a 27-year-old woman with fatigue ﻿

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry ﻿

Atlas of the clinical genetics of human 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 ﻿

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype ﻿

Diagnostic approach of idiopathic ventricular fibrillation: results from the FIVI-Gen study ﻿

Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study) ﻿

Doppler tisular y estratificación del riesgo en la miocardiopatía hipertrófica ﻿

Effects of Prolonged-Release Torasemide Versus Furosemide on Myocardial Fibrosis in Hypertensive Patients with Chronic Heart Failure: A Randomized, Blinded End Point, Active-Controlled Study ﻿

Enlarging the genetic spectrum of cardiomyopathies. Preliminary results of the myestela pediatric cohort study ﻿

Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy ﻿

Fabry disease: A new mutation with phenotypic correlation? ﻿

Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin Gene ﻿

A family with recurrent sudden death and no clinical clue

A gain-of-function HCN4 mutant in the HCN domain is responsible for inappropriate sinus tachycardia in a Spanish family

A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD)

A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy: A proof of concept study

A novel Troponin I mutation associated with severe restrictive cardiomyopathy - A case report of a 27-year-old woman with fatigue

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

Atlas of the clinical genetics of human 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

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype

Diagnostic approach of idiopathic ventricular fibrillation: results from the FIVI-Gen study

Diagnostic Approach to Unexplained Cardiac Arrest (from the FIVI-Gen Study)

Doppler tisular y estratificación del riesgo en la miocardiopatía hipertrófica

Effects of Prolonged-Release Torasemide Versus Furosemide on Myocardial Fibrosis in Hypertensive Patients with Chronic Heart Failure: A Randomized, Blinded End Point, Active-Controlled Study

Enlarging the genetic spectrum of cardiomyopathies. Preliminary results of the myestela pediatric cohort study

Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy

Fabry disease: A new mutation with phenotypic correlation?

Familial Recurrent Myocarditis Triggered by Exercise in Patients With a Truncating Variant of the Desmoplakin Gene