Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Eva Cabrera-Borrego"'
Autor:
Eva Cabrera Borrego, MD, Francisco José Bermúdez-Jiménez, PhD, MD, Rosa Macías Ruiz, MD, Francesca Perin, MD, Juan Jiménez-Jáimez, PhD, MD
Publikováno v:
JACC: Case Reports, Vol 2, Iss 6, Pp 935-937 (2020)
We present a case of sarcomeric hypertrophy cardiomyopathy diagnosed in a child who had hypertrophy degree regression during adolescence, with no left ventricular dysfunction and no increase of the ventricular diameters. (Level of Difficulty: Interme
Externí odkaz:
https://doaj.org/article/4a5e46102d0e4dee8ed2b2387ae7c00b
Autor:
Laura Valverde Soria, Manuel Molina-Lerma, Laura Jordán-Martínez, Francisco Bermúdez, Eva Cabrera Borrego, Miguel Álvarez
Publikováno v:
REC: CardioClinics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ba41025b347096f7381a48081fb7c9b
https://doi.org/10.1016/j.rccl.2023.05.002
https://doi.org/10.1016/j.rccl.2023.05.002
Autor:
Javier Ramos-Maqueda, Jairo H. Migueles, María Molina-Jiménez, David Ruiz-González, Eva Cabrera-Borrego, Amalio Ruiz-Salas, Alberto Soriano-Maldonado, Juan Jiménez-Jáimez
ObjectivesThis study aimed to investigate the association of accelerometer-measured lifestyle physical activity with the incidence of rapid-rate non-sustained ventricular tachycardias (RR-NSVT) during a 30-day recording period in AC patients.MethodsT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea36f63954bfebe21caa7ae979bc0bef
https://doi.org/10.1101/2022.07.27.22278124
https://doi.org/10.1101/2022.07.27.22278124
Autor:
Jesús G. Mirelis, Luis Escobar‐Lopez, Juan Pablo Ochoa, María Ángeles Espinosa, Eduardo Villacorta, Marina Navarro, Guillem Casas, Nerea Mora‐Ayestarán, Roberto Barriales‐Villa, María Victoria Mogollón‐Jiménez, José M. García‐Pinilla, Pablo E. García‐Granja, Vicente Climent, Julian Palomino‐Doza, Ana García‐Álvarez, María Álvarez‐Barredo, Eva Cabrera‐Borrego, Tomás Ripoll‐Vera, María Luisa Peña‐Peña, Elena Rodríguez‐González, María Gallego‐Delgado, Josefa Gonzalez‐Carrillo, Ana Fernández‐Ávila, José F. Rodríguez‐Palomares, Ramón Brugada, Antoni Bayes‐Genis, Fernando Dominguez, Pablo García‐Pavía
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
EUROPEAN JOURNAL OF HEART FAILURE
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
European Journal of Heart Failure
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
EUROPEAN JOURNAL OF HEART FAILURE
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
European Journal of Heart Failure
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Aims: Genotype and left ventricular scar on cardiac magnetic resonance (CMR) are increasingly recognized as risk markers for adverse outcomes in non-ischaemic dilated cardiomyopathy (DCM). We investigated the combined influence of genotype and late g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96fd5c901a5e0e09381b7c8d2212050a
https://hdl.handle.net/10668/21940
https://hdl.handle.net/10668/21940
Autor:
Javier Ramos-Maqueda, Jairo H Migueles, María Molina-Jiménez, David Ruiz-González, Eva Cabrera-Borrego, Amalio Ruiz Salas, Alberto Soriano-Maldonado, Juan Jimenez-Jaimez
Publikováno v:
Heart. :heartjnl-2022
Objective To investigate the association of accelerometer-measured lifestyle physical activity with rapid-rate non-sustained ventricular tachycardias (RR NSVTs) in patients with arrhythmogenic cardiomyopathy (AC). Methods This multicentre, observatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::877a49aafc15280e6e39be409b2351f2
https://doi.org/10.1136/heartjnl-2022-321824
https://doi.org/10.1136/heartjnl-2022-321824
Autor:
Eva, Cabrera-Borrego, Trinidad, Montero-Vilchez, Francisco José, Bermúdez-Jiménez, Jesús, Tercedor-Sánchez, Luis, Tercedor-Sánchez, Manuel, Sánchez-Díaz, Rosa, Macías-Ruiz, María, Molina-Jiménez, Francisco Javier, Cañizares-García, Eduardo, Fernández-Segura, Angel, Fernandez-Flores, Salvador, Arias-Santiago, Juan, Jiménez-Jáimez
Publikováno v:
Journal of Clinical Medicine
Genetic variants that result in truncation in desmoplakin (DSP) are a known cause of arrhythmogenic cardiomyopathy (AC). In homozygous carriers, the combined involvement of skin and heart muscle is well defined, however, this is not the case in heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5984788e692490fc3e5dbed13d94440a
https://pubmed.ncbi.nlm.nih.gov/34640625
https://pubmed.ncbi.nlm.nih.gov/34640625
Autor:
Francesca Perin, Rosa Macías Ruiz, Juan Jiménez-Jáimez, Eva Cabrera Borrego, Francisco Bermúdez-Jiménez
Publikováno v:
JACC: Case Reports, Vol 2, Iss 6, Pp 935-937 (2020)
JACC Case Reports
JACC Case Reports
We present a case of sarcomeric hypertrophy cardiomyopathy diagnosed in a child who had hypertrophy degree regression during adolescence, with no left ventricular dysfunction and no increase of the ventricular diameters. (Level of Difficulty: Interme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0d4b2fe4b714be8c9db2f24c71bb843
https://doi.org/10.1016/j.jaccas.2020.04.048
https://doi.org/10.1016/j.jaccas.2020.04.048
Autor:
Eduardo Fernández-Segura, Juan Jiménez-Jáimez, Angel Fernandez-Flores, Trinidad Montero-Vilchez, Francisco Javier Cañizares-García, Jesús Tercedor-Sánchez, Salvador Arias-Santiago, Eva Cabrera-Borrego, Francisco Bermúdez-Jiménez, María Molina-Jiménez, Rosa Macías-Ruiz, Luis Tercedor-Sánchez, Manuel Sánchez-Díaz
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Journal of Clinical Medicine
Volume 10
Issue 19
Journal of Clinical Medicine, Vol 10, Iss 4608, p 4608 (2021)
instname
Journal of Clinical Medicine
Volume 10
Issue 19
Journal of Clinical Medicine, Vol 10, Iss 4608, p 4608 (2021)
Genetic variants that result in truncation in desmoplakin (DSP) are a known cause of arrhythmogenic cardiomyopathy (AC). In homozygous carriers, the combined involvement of skin and heart muscle is well defined, however, this is not the case in heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76251629de84eaa90a9a6bf17bb1516f
http://hdl.handle.net/10481/70916
http://hdl.handle.net/10481/70916
Autor:
Lucía Torres-Quintero, Eva Cabrera-Borrego, Miguel A. Alvarez, Luis Tercedor-Sánchez, Rocío García-Orta, Manuel Molina-Lerma
Publikováno v:
JACC. Clinical electrophysiology. 6(6)
A mechanical tricuspid valve makes it difficult to implant a transvenous endocardial lead in the right ventricle, necessitating pacing by alternative nonphysiological methods such as implanting an epicardial lead and pacing through the coronary sinus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57d5dcbfafb8b72fef87be24dbdb228e
https://pubmed.ncbi.nlm.nih.gov/32553229
https://pubmed.ncbi.nlm.nih.gov/32553229