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12 results on '"Freire, Javier Limeres"'

1. Correlation Between Fibrosis and Malignant Arrhythmias in a Multicenter Cohort of Patients with Left Ventricular Arrhythmogenic Cardiomyopathy

Author

Freire, Javier Limeres, primary, Zorio, Esther, additional, Jimenez-Jaimez, Juan, additional, Achaga, Xabier Arana, additional, Pinilla, Jose Manuel García, additional, Ripoll, Tomas, additional, Payá, Vicente Climent, additional, García-Pavía, Pablo, additional, Díez-López, Carles, additional, Angeles Espinosa, M, additional, Bachiller, Rocio Eiros, additional, Barriales-Villa, Roberto, additional, Palomino-Doza, Julian, additional, Llano, Coloma Tiron de, additional, Peña, Maria Luisa Peña, additional, Masnou, Guillem Casas, additional, García-Moreno, Laura Gutierrez, additional, and Palomares, José F Rodríguez, additional

Published
2024
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2. Kiosk 2R-TA-06 - Predictive Risk Score for Ventricular Arrhythmias in a Multicenter Cohort of Left Ventricular Arrhythmogenic Cardiomyopathy Patients

Author

Freire, Javier Limeres, Zorio, Esther, Jimenez-Jaimez, Juan, Achaga, Xabier Arana, Pinilla, Jose Manuel García, Ripoll, Tomas, Payá, Vicente Climent, García-Pavía, Pablo, Díez-López, Carles, Angeles Espinosa, M, Bachiller, Rocio Eiros, Barriales-Villa, Roberto, Palomino-Doza, Julian, Llano, Coloma Tiron de, Peña, Maria Luisa Peña, Masnou, Guillem Casas, García-Moreno, Laura Gutierrez, and Rodríguez Palomares, José F

Published
2024
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3. CMR 2-74 - Correlation Between Fibrosis and Malignant Arrhythmias in a Multicenter Cohort of Patients with Left Ventricular Arrhythmogenic Cardiomyopathy

Author

Freire, Javier Limeres, Zorio, Esther, Jimenez-Jaimez, Juan, Achaga, Xabier Arana, Pinilla, Jose Manuel García, Ripoll, Tomas, Payá, Vicente Climent, García-Pavía, Pablo, Díez-López, Carles, Angeles Espinosa, M, Bachiller, Rocio Eiros, Barriales-Villa, Roberto, Palomino-Doza, Julian, Llano, Coloma Tiron de, Peña, Maria Luisa Peña, Masnou, Guillem Casas, García-Moreno, Laura Gutierrez, and Palomares, José F Rodríguez

Published
2024
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4. Emery–Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure.

Author

Cannie, Douglas E, Syrris, Petros, Protonotarios, Alexandros, Bakalakos, Athanasios, Pruny, Jean-François, Ditaranto, Raffaello, Martinez-Veira, Cristina, Larrañaga-Moreira, Jose M, Medo, Kristen, Bermúdez-Jiménez, Francisco José, Yaou, Rabah Ben, Leturcq, France, Mezcua, Ainhoa Robles, Marini-Bettolo, Chiara, Cabrera, Eva, Reuter, Chloe, Freire, Javier Limeres, Rodríguez-Palomares, José F, Mestroni, Luisa, and Taylor, Matthew R G

Subjects
VENTRICULAR arrhythmia, MUSCULAR dystrophy, HEART failure, ATRIAL arrhythmias, IMPLANTABLE cardioverter-defibrillators, CARDIOMYOPATHIES
Abstract

Background and Aims Emery–Dreifuss muscular dystrophy (EDMD) is caused by variants in EMD (EDMD1) and LMNA (EDMD2). Cardiac conduction defects and atrial arrhythmia are common to both, but LMNA variants also cause end-stage heart failure (ESHF) and malignant ventricular arrhythmia (MVA). This study aimed to better characterize the cardiac complications of EMD variants. Methods Consecutively referred EMD variant-carriers were retrospectively recruited from 12 international cardiomyopathy units. MVA and ESHF incidences in male and female variant-carriers were determined. Male EMD variant-carriers with a cardiac phenotype at baseline (EMD CARDIAC) were compared with consecutively recruited male LMNA variant-carriers with a cardiac phenotype at baseline (LMNA CARDIAC). Results Longitudinal follow-up data were available for 38 male and 21 female EMD variant-carriers [mean (SD) ages 33.4 (13.3) and 43.3 (16.8) years, respectively]. Nine (23.7%) males developed MVA and five (13.2%) developed ESHF during a median (inter-quartile range) follow-up of 65.0 (24.3–109.5) months. No female EMD variant-carrier had MVA or ESHF, but nine (42.8%) developed a cardiac phenotype at a median (inter-quartile range) age of 58.6 (53.2–60.4) years. Incidence rates for MVA were similar for EMD CARDIAC and LMNA CARDIAC (4.8 and 6.6 per 100 person-years, respectively; log-rank P =.49). Incidence rates for ESHF were 2.4 and 5.9 per 100 person-years for EMD CARDIAC and LMNA CARDIAC, respectively (log-rank P =.09). Conclusions Male EMD variant-carriers have a risk of progressive heart failure and ventricular arrhythmias similar to that of male LMNA variant-carriers. Early implantable cardioverter defibrillator implantation and heart failure drug therapy should be considered in male EMD variant-carriers with cardiac disease. [ABSTRACT FROM AUTHOR]

Published
2023
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5. 5. PENETRANCIA DE LA MIOCARDIOPATÍA DILATADA EN PORTADORES GENÉTICOS

Author

Romero, Eva Cabrera, Barrio, Roberto Barriales, Jiménez, Francisco José Bermúdez, Paya, Vicent Climent, González, Cristina Gómez, Martínez, José Carlos Sánchez, Delgado, María Gallego, Peñalver, Marina Navarro, Achaga, Xabier Arana, Flores, Jesús Piqueras, Bares, Victoria Espejo, Lecumberri, Gemma Lacuey, Freire, Javier Limeres, Díaz, Javier López, and Pavía, Pablo García

Published
2023
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6. 2. EL ANÁLISIS EXHAUSTIVO DE RMC MEJORA LA ESTRATIFICACIÓN PRONÓSTICA EN NO COMPACTACIÓN DEL VENTRÍCULO IZQUIERDO

Author

Masnou, Guillem Casas, Alesina, Eduardo Ródenas, del Hoyo, María Isabel González, Villa, Roberto Barriales, Mirelis, Jesús González, Argüelles, Eduardo Villacorta, Grima, Esther Zorio, Jáimez, Juan Jiménez, Soley, Albert Téis, Vera, Tomás Ripoll, Carrillo, Josefa González, Guala, Andrea, Freire, Javier Limeres, González, Ignacio Ferreira, and Palomares, José Fernando Rodríguez

Published
2023
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7. Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator

Author

Protonotarios, Alexandros, primary, Bariani, Riccardo, additional, Cappelletto, Chiara, additional, Pavlou, Menelaos, additional, García-García, Alba, additional, Cipriani, Alberto, additional, Protonotarios, Ioannis, additional, Rivas, Adrian, additional, Wittenberg, Regitze, additional, Graziosi, Maddalena, additional, Xylouri, Zafeirenia, additional, Larrañaga-Moreira, José M, additional, de Luca, Antonio, additional, Celeghin, Rudy, additional, Pilichou, Kalliopi, additional, Bakalakos, Athanasios, additional, Lopes, Luis Rocha, additional, Savvatis, Konstantinos, additional, Stolfo, Davide, additional, Dal Ferro, Matteo, additional, Merlo, Marco, additional, Basso, Cristina, additional, Freire, Javier Limeres, additional, Rodriguez-Palomares, Jose F, additional, Kubo, Toru, additional, Ripoll-Vera, Tomas, additional, Barriales-Villa, Roberto, additional, Antoniades, Loizos, additional, Mogensen, Jens, additional, Garcia-Pavia, Pablo, additional, Wahbi, Karim, additional, Biagini, Elena, additional, Anastasakis, Aris, additional, Tsatsopoulou, Adalena, additional, Zorio, Esther, additional, Gimeno, Juan R, additional, Garcia-Pinilla, Jose Manuel, additional, Syrris, Petros, additional, Sinagra, Gianfranco, additional, Bauce, Barbara, additional, and Elliott, Perry M, additional

Published
2022
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8. 3. EFECTO FUNDADOR DE LA VARIANTE GENÉTICA P.ASN271ILE EN TNNT2 EN A CORUÑA ASOCIADA A MIOCARDIOPATÍA HIPERTRÓFICA DE PRONÓSTICO BENIGNO

Author

Moreira, José María Larrañaga, Deben, Rosalía Peteiro, Argüelles, Eduardo Villacorta, Peña, María Luisa Peña, Serrano, Ana Isabel Rodríguez, Fernández, Adrián, Palomino-Doza, Julián, Freire, Javier Limeres, Acevedo, Olga, Vilela, Alejandro Rodríguez, Gutiérrez, Rebeca Lorca, Vera, Tomás Ripoll, Gutiérrez, Raúl Franco, Folmer, Juan Pablo Ochoa, and Villa, Roberto Barriales

Published
2023
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9. 5. IMPACTO DEL GENOTIPO EN LA RESPUESTA A TRATAMIENTO MÉDICO A LARGO PLAZO EN MIOCARDIOPATÍA DILATADA NO ISQUÉMICA

Author

Ayestarán, Nerea Mora, Mirelis, Jesús González, Castro, Mª Ángeles Espinosa, Peñalver, Marina Navarro, Delgado, María Gallego, Villa, Roberto Barriales, Payá, Vicente Climent, Mezcua, Ainhoa Robles, Jiménez, María Victoria Mogollón, Peña, María Luisa Peña, Freire, Javier Limeres, Elorz, Mayte Basurte, Álvarez, Ana García, Calderon, Germán Cediel, and Pavía, Pablo García

Published
2023
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10. Predictive Risk Score for Ventricular Arrhythmias in a Multicenter Cohort of Left Ventricular Arrhythmogenic Cardiomyopathy Patients

Author

Freire, Javier Limeres, Zorio, Esther, Jimenez-Jaimez, Juan, Achaga, Xabier Arana, Pinilla, Jose Manuel García, Ripoll, Tomas, Payá, Vicente Climent, García-Pavía, Pablo, Díez-López, Carles, Angeles Espinosa, M, Bachiller, Rocio Eiros, Barriales-Villa, Roberto, Palomino-Doza, Julian, Llano, Coloma Tiron de, Peña, Maria Luisa Peña, Masnou, Guillem Casas, García-Moreno, Laura Gutierrez, and Rodríguez Palomares, José F

Published
2024
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11. 17. RESULTADOS PRELIMINARES DEL REGISTRO ESPAÑOL DE AMILOIDOSIS HEREDITARIA POR TRANSTIRRETINA

Author

Federik, Guadalupe Noel, Burgos, Carlos Miguel Veras, Pericet, Cristina, Costello, José González, Sánchez, Ana José Manovel, Grima, Esther Zorio, Linares, Jaume Pons, Pinilla, José Manuel García, Sierra, Lucas Tojal, Freire, Javier Limeres, Blanes, Juan Ramón Gimeno, Álvarez, Ana García, Ruíz, Rosa Macías, Castro, Mª Ángeles Espinosa, and Vera, Tomás Ripoll

Published
2023
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12. Caracterización de la amiloidosis cardiaca hereditaria por transtirretina en España

Author

Rubio, Jorge Alvarez, Sánchez, Ana José Manovel, González-Costello, José, García-Pavía, Pablo, Freire, Javier Limeres, García-Pinilla, José Manuel, Grima, Esther Zorio, García-Álvarez, Ana, Gómez, María Valverde, castro, M. Ángeles espinosa, Barge-Caballero, Gonzalo, Blanes, Juan Ramón Gimeno, Rovira, María Teresa Bosch, Díaz, Luis Miguel Rincón, Arregui, Miguel Ángel Aibar, Gallego-Delgado, María, Jiménez-Jáimez, Juan, Moreno, Marina Martínez, Basurte, Mayte, Achaga, Xabier Arana, Baldomero, Idaira Famara Hernández, and Ripoll-Vera, Tomás

Abstract

La amiloidosis hereditaria por transtirretina (ATTRv) es una enfermedad causada por mutaciones en el gen de la transtirretina que frecuentemente presenta afección cardiaca debido al depósito de amiloide en el miocardio. Nuestro objetivo es describir esta afección en una cohorte española.

Published
2021
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