Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Fernando Cabrera-Bueno"'
Autor:
Víctor Manuel Becerra-Muñoz, Juan José Gómez-Doblas, Carlos Porras-Martín, Miguel Such-Martínez, María Generosa Crespo-Leiro, Roberto Barriales-Villa, Eduardo de Teresa-Galván, Manuel Jiménez-Navarro, Fernando Cabrera-Bueno
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Abstract Background Marfan syndrome (MFS) is a disorder of autosomal dominant inheritance, in which aortic root dilation is the main cause of morbidity and mortality. Fibrillin-1 (FBN-1) gene mutations are found in more than 90% of MFS cases. The aim
Externí odkaz:
https://doaj.org/article/0c92ad7c36514b2d9a28d7edeaf8eba8
Autor:
Víctor M. Becerra-Muñoz, Arancha Díaz-Expósito, Victoria Doncel-Abad, Patricia Fernández-García, José Luis López-Benítez, Fernando Cabrera-Bueno
Publikováno v:
Revista Española de Cardiología. 75:766-768
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::007ad9053c249308eb20b18c29d205f5
https://doi.org/10.1016/j.recesp.2022.02.005
https://doi.org/10.1016/j.recesp.2022.02.005
Autor:
Víctor M. Becerra-Muñoz, Arancha Díaz-Expósito, Victoria Doncel-Abad, Patricia Fernández-García, José Luis López-Benítez, Fernando Cabrera-Bueno
Publikováno v:
Revista Española de Cardiología (English Edition). 75:765-767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3e5467a8c001df19759b9e108075727
https://doi.org/10.1016/j.rec.2022.02.014
https://doi.org/10.1016/j.rec.2022.02.014
Usefulness of Genetic Study by Next-generation Sequencing in High-risk Arrhythmogenic Cardiomyopathy
Autor:
Amalio Ruiz Salas, Ana Guijarro, José Manuel García Pinilla, Carmen Medina Palomo, Juan José Gómez Doblas, Manuel Jiménez Navarro, Fernando Cabrera Bueno, Javier Alzueta, José Peña Hernández, Eduardo de Teresa, Luis Morcillo-Hidalgo, Alberto Barrera Cordero
Publikováno v:
Revista Española de Cardiología (English Edition). 71:1018-1026
Introduction and objectives Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by progressive fibrofatty replacement of predominantly right ventricular myocardium . This cardiomyopathy is a frequent ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25fe1acc1ea00085529ac4d363547caa
https://doi.org/10.1016/j.rec.2018.03.001
https://doi.org/10.1016/j.rec.2018.03.001
Autor:
Manuel Jiménez Navarro, Amalio Ruiz Salas, José Peña Hernández, Luis Morcillo-Hidalgo, Juan José Gómez Doblas, Fernando Cabrera Bueno, Carmen Medina Palomo, José Manuel García Pinilla, Javier Alzueta, Alberto Barrera Cordero, Ana Guijarro, Eduardo de Teresa
Publikováno v:
Revista Española de Cardiología. 71:1018-1026
Resumen Introduccion y objetivos La miocardiopatia arritmogenica del ventriculo derecho (MCAVD) es una cardiopatia hereditaria definida por la sustitucion progresiva de miocardio ventricular derecho por tejido fibroadiposo. Es causa frecuente de la m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6a9441a482526f5040444ff6191beb4
https://doi.org/10.1016/j.recesp.2017.11.007
https://doi.org/10.1016/j.recesp.2017.11.007
Autor:
Eduardo de Teresa, Fernando Cabrera Bueno, Nasiba Abdeselam-Mohamed, Isabel Navarro‐Arce, Juan José Gómez Doblas, José Manuel García Pinilla, Amalio Ruiz Salas, Manuel Jiménez Navarro, Alberto Barrera Cordero, Javier Alzueta, Luis Morcillo-Hidalgo
Publikováno v:
Journal of Cardiovascular Electrophysiology. 29:1523-1529
INTRODUCTION Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited cardiomyopathy characterized by ventricular arrhythmias and heart failure. The variable phenotype suggesting that determined environmental factors may hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b101f5e084bcb4c2e37bbc83db7b501e
https://doi.org/10.1111/jce.13704
https://doi.org/10.1111/jce.13704
Publikováno v:
Cardiocore. 52:51-56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d93d777f6e3a0252e25272ee1f31b80c
https://doi.org/10.1016/j.carcor.2017.03.001
https://doi.org/10.1016/j.carcor.2017.03.001
Autor:
Amalio Ruiz-Salas, Isabel Navarro-Arce, Carmen Medina-Palomo, Alberto Barrera-Cordero, Manuel Jiménez-Navarro, Eloy Rueda-Calle, José Manuel García-Pinilla, Fernando Cabrera-Bueno, Luis Morcillo-Hidalgo, Juan José Gómez-Doblas, Javier Alzueta
Background: Arrhythmogenic right ventricular cardiomyopathy (ARVC/D) is an inherited cardiomyopathy characterized by ventricular arrhythmias and heart failure. The aim of our study was to analyze the impact of the ICD indication in the prognosis of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2cc8f47ab812918269ec1dca918d4ae
https://doi.org/10.21203/rs.2.16672/v1
https://doi.org/10.21203/rs.2.16672/v1
Autor:
Luis Morcillo-Hidalgo, Fernando Cabrera-Bueno, Ana Isabel Molina-Ramos, Fernando Carrasco-Chinchilla
Publikováno v:
REC: CardioClinics. 56:59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0d53be2f6598cdd0c3cf1f555cc1825
https://doi.org/10.1016/j.rccl.2020.05.002
https://doi.org/10.1016/j.rccl.2020.05.002
Autor:
Juan José Gómez-Doblas, Víctor Manuel Becerra-Muñoz, Fernando Cabrera-Bueno, Manuel F. Jiménez-Navarro, María G. Crespo-Leiro, Eduardo de Teresa-Galván, Roberto Barriales-Villa, Carlos Porras-Martín, Miguel Such-Martínez
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Background Marfan syndrome (MFS) is a disorder of autosomal dominant inheritance, in which aortic root dilation is the main cause of morbidity and mortality. Fibrillin-1 (FBN-1) gene mutations are found in more than 90% of MFS cases. The aim of our s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc0bf0389f9466d7498e463320af3c0
https://hdl.handle.net/10668/12035
https://hdl.handle.net/10668/12035