Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Juan R. Gimeno Blanes"'
Autor:
Juan R. Gimeno Blanes
Publikováno v:
CorSalud, Vol 9, Iss 3, Pp 218-219 (2017)
En los últimos dos años se han publicado trabajos importantes sobre la miocardiopatía hipertrófica (MCH). Desde el punto de vista clínico quizás el más relevante ha sido la publicación de las Guías de Diagnóstico y Tratamiento de la MCH de
Externí odkaz:
https://doaj.org/article/0efaa1c419aa41eeae5b6678a569f7a2
Autor:
Maria Sabater Molina, Elisa Nicolás Rocamora, Asunción Iborra Bendicho, Elisa García Vázquez, Esther Zorio, Fernando Domínguez Rodriguez, Cristina Gil Ortuño, Ana Isabel Rodríguez, Antonio J Sánchez-López, Rubén Jara Rubio, Antonio Moreno-Docón, Pedro J Marcos, Pablo García Pavía, Roberto Barriales Villa, Juan R Gimeno Blanes
Publikováno v:
PLoS ONE, Vol 17, Iss 2, p e0263140 (2022)
BackgroundInfection by the SARS-Cov-2 virus produces in humans a disease of highly variable and unpredictable severity. The presence of frequent genetic single nucleotide polymorphisms (SNPs) in the population might lead to a greater susceptibility t
Externí odkaz:
https://doaj.org/article/c2363fd06a5b4672831a8938afe0b115
Autor:
Marcos Siguero-Álvarez, Alejandro Salguero-Jiménez, Joaquim Grego-Bessa, Jorge de la Barrera, Donal MacGrogan, Belén Prados, Fernando Sánchez-Sáez, Rebeca Piñeiro-Sabarís, Natalia Felipe-Medina, Carlos Torroja, Manuel José Gómez, María Sabater-Molina, Rubén Escribá, Ivonne Richaud-Patin, Olalla Iglesias-García, Mauro Sbroggio, Sergio Callejas, Declan P. O’Regan, Kathryn A. McGurk, Ana Dopazo, Giovanna Giovinazzo, Borja Ibañez, Lorenzo Monserrat, José María Pérez-Pomares, Fátima Sánchez-Cabo, Alberto M. Pendas, Angel Raya, Juan R. Gimeno-Blanes, José Luis de la Pompa
The complex genetics underlying human cardiac disease is evidenced by its heterogenous manifestation, multigenic basis, and sporadic occurrence. These features have hampered disease modeling and mechanistic understanding. Here, we show that 2 structu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c9d5c2f3da4e9446d77a979ec3f9f2
http://hdl.handle.net/2445/193600
http://hdl.handle.net/2445/193600
Autor:
Esperanza, García-Molina, María, Sabater-Molina, David, López-Cuenca, María C, Olmo, Inmaculada, Pérez, Carmen, Muñoz Esparza, Juan R, Gimeno Blanes
Publikováno v:
American journal of translational research. 11(3)
With the development of deep sequencing, a significant proportion of mutations already listed in studies have inconclusive pathogenicity. We aim to establish the proportion of cases in which familial studies are possible and cosegregation analysis is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::002159c9a5d7b565840452c8c035d10d
https://pubmed.ncbi.nlm.nih.gov/30972196
https://pubmed.ncbi.nlm.nih.gov/30972196