Zobrazeno 1 - 8
of 8
pro vyhledávání: '"M. J. Curras-Tuala"'
Autor:
J. Gómez-Rial, M. J. Curras-Tuala, C. Talavero-González, C. Rodríguez-Tenreiro, L. Vilanova-Trillo, A. Gómez-Carballa, I. Rivero-Calle, A. Justicia-Grande, J. Pardo-Seco, L. Redondo-Collazo, A. Salas, F. Martinón-Torres
Publikováno v:
BMC Infectious Diseases, Vol 17, Iss 1, Pp 1-5 (2017)
Abstract Background The IFI27 interferon gene expression has been found to be largely increased in rotavirus (RV)-infected patients. IFI27 gene encodes for a protein of unknown function, very recently linked to epidermal proliferation and related to
Externí odkaz:
https://doaj.org/article/905ff69de02f4cf19cd0691a865013b2
Autor:
José María Martinón-Martínez, Federico Martinón-Torres, M. J. Curras-Tuala, Irene Rivero-Calle, J. Vilar, José Gómez-Rial, Ruth Barral-Arca, Antonio José Justicia-Grande, Jacobo Pardo-Seco, Antonio Salas, Miriam Cebey-López, Sara Pischedda
Publikováno v:
Vaccine. 37(25)
There is a growing interest in the possible relationship between rotavirus (RV) vaccine and hospitalizations due to childhood seizures. We explored variation in hospitalization rates after 9 years of vaccination against pre-vaccination period for chi
Autor:
Alberto Gómez-Carballa, Jacobo Pardo-Seco, Lorenzo Redondo-Collazo, C. Talavero-González, José Gómez-Rial, Federico Martinón-Torres, Irene Rivero-Calle, Lucía Vilanova-Trillo, Carmen Rodríguez-Tenreiro, Antonio José Justicia-Grande, M. J. Curras-Tuala, Antonio Salas
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
BMC Infectious Diseases, Vol 17, Iss 1, Pp 1-5 (2017)
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
BMC Infectious Diseases
instname
BMC Infectious Diseases, Vol 17, Iss 1, Pp 1-5 (2017)
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
BMC Infectious Diseases
Background:TheIFI27interferon gene expression has been found to be largely increased in rotavirus (RV)-infectedpatients.IFI27gene encodes for a protein of unknown function, very recently linked to epidermal proliferation andrelated to the epidermal g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a3e71b42fe12bd05fa13fa1f83cd00a
http://hdl.handle.net/10347/22407
http://hdl.handle.net/10347/22407
Autor:
Federico Martinón-Torres, Ana Vega, J I Muñoz Bonet, Á Ortega, J López-Bayón, Sara Pischedda, Martin L. Hibberd, M C León León, A B Arriortua, C P Caballero Macarrón, M L Millán Miralles, Victoria J. Wright, Simon Nadel, Kar Seng Sim, E E Torné, Nazareth Martinón-Torres, García, A H Doce, F G Sánchez, Ruth Barral-Arca, Dominguez, R Payo, F P Sánchez, J M Sánchez Granados, Carmen Rodríguez-Tenreiro, E Morteruel, M S Cancela, Á Barba, N G Sánchez, M. J. Curras-Tuala, Jacobo Pardo-Seco, E O Bergara, M L Navarro Gómez, David Inwald, S P Rosso, Sergio Alonso, Marcela Fernández, Garzón Mgr., A R Romero, J De La Cruz Moreno, Antonio Salas, García Mdmb., A J Grande, C C Monge, A C Torre, Enitan D. Carrol, S C Palazón, Laura Fachal, N M Menchón, J L García Rodríguez, M O Pallares, Michael Levin, Sonia Davila, O S Ayestarán, Alberto Gómez-Carballa, Chiea Chuen Khor, Irene Rivero Calle, Miriam Cebey, De Aguilar Pag., Eileen Png, Angel Carracedo, José María Martinón-Sánchez, Xavier Martinez, Martínez-Padilla Mdc., Lorenzo Redondo-Collazo
Publikováno v:
SCIENTIFIC REPORTS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Scientific Reports
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Scientific Reports
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Meningococcal disease (MD) remains an important infectious cause of life threatening infection in both industrialized and resource poor countries. Genetic factors influence both occurrence and severity of presentation, but the genes responsible are l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e76b4694e9027a3e9e0ef1a81eaf55ff
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994338378&doi=10.1038/srep35842&partnerID=40&md5=aa562f1e1488515cd4ae335d0fa163ae
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84994338378&doi=10.1038/srep35842&partnerID=40&md5=aa562f1e1488515cd4ae335d0fa163ae
Autor:
M. Cebey-López, M. J. Currás-Tuala, J. Gómez-Rial, I. Rivero-Calle, J. Pardo-Seco, R. Mendez-Gallart, S. Pischedda, A. Gómez-Carballa, R. Barral-Arca, A. Justicia-Grande, S. Viz-Lasheras, C. Rodríguez-Tenreiro, R. Gómez, A. Salas, F. Martinón-Torres
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundProgressive osseous heteroplasia (POH) is an ultrarare genetic disorder characterized by an inactivating mutation in the GNAS gene that causes heterotopic ossification. Inhibition of the mammalian target of the rapamycin (mTOR) signalling p
Externí odkaz:
https://doaj.org/article/739d029c73ca497da3f84a32bf92c5c3
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