Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Rocío, Toro"'
Autor:
Elena Arbelo, Gonzalo Grazioli, Carles Díez-López, Oscar Campuzano, Georgia Sarquella-Brugada, Sergi Cesar, Estefanía Martínez-Barrios, Rocío Toro, José Cruzalegui, Andrea Greco, Nuria Díez-Escuté, Patricia Cerralbo, Fredy Chipa, Norma Balderrábano
Publikováno v:
BMJ Open Sport & Exercise Medicine, Vol 10, Iss 3 (2024)
Sudden cardiac death is a rare but socially devastating event, especially if occurs in young people. Usually, this unexpected lethal event occurs during or just after exercise. One of the leading causes of sudden cardiac death is inherited arrhythmog
Externí odkaz:
https://doaj.org/article/d98a2bce5c9d4002abe937027884e2b4
Autor:
Fernando Bonet, Oscar Campuzano, José Córdoba-Caballero, Mireia Alcalde, Georgia Sarquella-Brugada, Aitana Braza-Boïls, Ramon Brugada, Francisco Hernández-Torres, Maribel Quezada-Feijoo, Monica Ramos, Alipio Mangas, Juan A. G. Ranea, Rocío Toro
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1807 (2024)
Arrhythmogenic cardiomyopathy is an inherited entity characterized by irregular cell–cell adhesion, cardiomyocyte death and fibro-fatty replacement of ventricular myocytes, leading to malignant ventricular arrythmias, contractile dysfunction and su
Externí odkaz:
https://doaj.org/article/945d2dc181984d7480a2a40bb22752e5
Autor:
Alexandra Pérez-Serra, Rocío Toro, Estefanía Martinez-Barrios, Anna Iglesias, Anna Fernandez-Falgueras, Mireia Alcalde, Mónica Coll, Marta Puigmulé, Bernat del Olmo, Ferran Picó, Laura Lopez, Elena Arbelo, Sergi Cesar, Coloma Tiron de Llano, Alipio Mangas, Josep Brugada, Georgia Sarquella-Brugada, Ramon Brugada, Oscar Campuzano
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 7, p 3807 (2024)
Dilated cardiomyopathy is a heterogeneous entity that leads to heart failure and malignant arrhythmias. Nearly 50% of cases are inherited; therefore, genetic analysis is crucial to unravel the cause and for the early identification of carriers at ris
Externí odkaz:
https://doaj.org/article/6b47b07d738b4660af7c8147b2ee20e1
Autor:
Mónica, Ramos-Sánchez, Maribel, Quezada-Feijoó, Javier, Jaramillo, Isabel, Lozano-Montoya, Rocío, Toro, Rocío, Ayala, Javier, Gómez-Pavón Francisco
Publikováno v:
In Revista Espanola de Geriatria y Gerontologia March-April 2022 57(2):63-70
Autor:
Estefanía Martínez-Barrios, Simone Grassi, María Brión, Rocío Toro, Sergi Cesar, José Cruzalegui, Mònica Coll, Mireia Alcalde, Ramon Brugada, Andrea Greco, María Luisa Ortega-Sánchez, Eneko Barberia, Antonio Oliva, Georgia Sarquella-Brugada, Oscar Campuzano
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
In the forensic medicine field, molecular autopsy is the post-mortem genetic analysis performed to attempt to unravel the cause of decease in cases remaining unexplained after a comprehensive forensic autopsy. This negative autopsy, classified as neg
Externí odkaz:
https://doaj.org/article/82adbe2de4bf4080a5976d662351f2d2
Autor:
Elena Alonso-Villa, Fernando Bonet, Francisco Hernandez-Torres, Óscar Campuzano, Georgia Sarquella-Brugada, Maribel Quezada-Feijoo, Mónica Ramos, Alipio Mangas, Rocío Toro
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 21, p 13573 (2022)
Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or biventricular dilation and systolic dysfunction. In most cases, DCM is progressive, leading to heart failure (HF) and death. This cardiomyopathy has been consid
Externí odkaz:
https://doaj.org/article/90ca7389ad324eb79ebe6b4d61bdd68d
Autor:
Estefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, Anna Fernandez-Falgueras, Sergi Cesar, Mireia Alcalde, Mónica Coll, Marta Puigmulé, Anna Iglesias, Carles Ferrer-Costa, Bernat del Olmo, Ferran Picó, Laura Lopez, Victoria Fiol, José Cruzalegui, Clara Hernandez, Elena Arbelo, Nuria Díez-Escuté, Patricia Cerralbo, Simone Grassi, Antonio Oliva, Rocío Toro, Josep Brugada, Ramon Brugada, Oscar Campuzano
Publikováno v:
International Journal of Legal Medicine. 137:345-351
Sudden death cases in the young population remain without a conclusive cause of decease in almost 40% of cases. In these situations, cardiac arrhythmia of genetic origin is suspected as the most plausible cause of death. Molecular autopsy may reveal
Autor:
Oscar Campuzano, Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Mónica Coll, Anna Iglesias, Carles Ferrer-Costa, Sergi Cesar, Elena Arbelo, Ana García-Álvarez, Paloma Jordà, Rocío Toro, Coloma Tiron de Llano, Simone Grassi, Antonio Oliva, Josep Brugada, Ramon Brugada
Publikováno v:
EBioMedicine, Vol 54, Iss , Pp - (2020)
ABSTRACT: Background: Accurate interpretation of rare genetic variants is a challenge for clinical translation. Updates in recommendations for rare variant classification require the reanalysis and reclassification. We aim to perform an exhaustive re
Externí odkaz:
https://doaj.org/article/0601828445ac458586eabbefcbeaf019
Autor:
Rocío Toro, Alexandra Pérez-Serra, Alipio Mangas, Oscar Campuzano, Georgia Sarquella-Brugada, Maribel Quezada-Feijoo, Mónica Ramos, Martin Alcalá, Esther Carrera, Carlos García-Padilla, Diego Franco, Fernando Bonet
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 3, p 1036 (2022)
Oxidative stress, defined as the excess production of reactive oxygen species (ROS) relative to antioxidant defense, plays a significant role in the development of cardiovascular diseases. Endoplasmic reticulum (ER) stress has emerged as an important
Externí odkaz:
https://doaj.org/article/7f490d85e1f8443a977b3d022f214396
Autor:
Leopoldo Pérez de Isla, Adriana Saltijeral, Jesus Millán Nuñez-Cortes, José Angel García Saez, Fernando Moreno, Joaquín Millan-Perez, Rocío Toro
Publikováno v:
Educación Médica, Vol 19, Iss 2, Pp 91-95 (2018)
Resumen: Objetivo: Comprobar los resultados de un entrenamiento en habilidad para realizar ecocardioscopias para oncólogos por parte de cardiólogos y estudiar la variabilidad en las mediciones y la significación clínica de esa variabilidad. Méto
Externí odkaz:
https://doaj.org/article/623f0479bff34a41a0530a58189f170f