Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Juan Ignacio, Aróstegui"'
Autor:
Aina Oliver-Caldes, Juan Carlos Soler-Perromat, Ester Lozano, David Moreno, Alex Bataller, Pablo Mozas, Marta Garrote, Xavier Setoain, Juan Ignacio Aróstegui, Jordi Yagüe, Natalia Tovar, Raquel Jiménez, Luis Gerardo Rodríguez-Lobato, M. Teresa Cibeira, Laura Rosiñol, Joan Bladé, Manel Juan, Carlos Fernández de Larrea
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
IntroductionMultiple myeloma (MM) is considered an incurable hematological neoplasm. For transplant-eligible patients, initial treatment includes an induction phase followed by an autologous stem cell transplantation (ASCT). Despite the introduction
Externí odkaz:
https://doaj.org/article/e5fabab14d0d45a2ac2c95f79c8116fd
Autor:
Jordi Sintes, Maurizio Gentile, Shuling Zhang, Yolanda Garcia-Carmona, Giuliana Magri, Linda Cassis, Daniel Segura-Garzón, Alessandra Ciociola, Emilie K. Grasset, Sabrina Bascones, Laura Comerma, Marc Pybus, David Lligé, Irene Puga, Cindy Gutzeit, Bing He, Wendy DuBois, Marta Crespo, Julio Pascual, Anna Mensa, Juan Ignacio Aróstegui, Manel Juan, Jordi Yagüe, Sergi Serrano, Josep Lloreta, Eric Meffre, Michael Hahne, Charlotte Cunningham-Rundles, Beverly A. Mock, Andrea Cerutti
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-16 (2017)
Marginal zone B cells differentiate into plasma cells rapidly in response to T-cell-independent antigens, but how they do so is not clear. Here the authors show TACI cooperates with TLR signalling to drive mTOR activity and subsequent class switching
Externí odkaz:
https://doaj.org/article/55fa5c77ea474673980a024897c7214c
Autor:
Guillem de Valles-Ibáñez, Ana Esteve-Solé, Mònica Piquer, E. Azucena González-Navarro, Jessica Hernandez-Rodriguez, Hafid Laayouni, Eva González-Roca, Ana María Plaza-Martin, Ángela Deyà-Martínez, Andrea Martín-Nalda, Mónica Martínez-Gallo, Marina García-Prat, Lucía del Pino-Molina, Ivón Cuscó, Marta Codina-Solà, Laura Batlle-Masó, Manuel Solís-Moruno, Tomàs Marquès-Bonet, Elena Bosch, Eduardo López-Granados, Juan Ignacio Aróstegui, Pere Soler-Palacín, Roger Colobran, Jordi Yagüe, Laia Alsina, Manel Juan, Ferran Casals
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Common variable immunodeficiency (CVID) is the most frequent symptomatic primary immunodeficiency characterized by recurrent infections, hypogammaglobulinemia and poor response to vaccines. Its diagnosis is made based on clinical and immunological cr
Externí odkaz:
https://doaj.org/article/101b88bc2f1f4640aaf1b70c55b35578
Autor:
Francisco José Nicolás-Sánchez, Rosa María Sarrat-Nuevo, Francesc Josep Nicolás-Sarrat, Juan Ignacio Aróstegui-Gorospe, Ramon María Nogue Bou, Judit Pallarés-Quixal, Pablo Melgarejo-Moreno
Publikováno v:
Reumatología Clínica. 17:46-48
Secondary amyloidosis can be found in some monogenic autoinflammatory diseases. In this study we present an 83-year-old man with no relevant medical history who presented with iron deficiency anaemia. In the study, a gastroscopy was performed with du
Autor:
Francisco José Nicolás-Sánchez, Juan Ignacio Aróstegui-Gorospe, Judit Pallarés-Quixal, Francesc Josep Nicolás-Sarrat, Rosa María Sarrat-Nuevo, Ramon María Nogue Bou, Pablo José Melgarejo-Moreno
Publikováno v:
Reumatología Clínica (English Edition). 17:46-48
Autor:
Carmen, Vargas Lebrón, Maria Dolores, Ruiz Montesino, Virginia, Moreira Navarrete, Juan Ignacio, Aróstegui Gorospe
Publikováno v:
Reumatología Clínica (English Edition). 16:499-501
Trichorhinophalangeal syndrome I (TPRSI) has an autosomal dominant inheritance; the proportion of «de novo» cases is unknown
Autor:
Caverzaschi, Verónica Gómez, Ribes, Jordi Yagüe, Garriga, Gerard Espinosa, Loperena, Olga Araújo, Segura, Ricard Cervera, Gorospe, Juan Ignacio Arostegui, Vilaró, Anna Mensa, Rodríguez, José Hernández
Publikováno v:
In Revista clinica espanola November 2023 223 Supplement 2:S203-S204
Publikováno v:
Pediatric dermatology. 33(6)
Specific gene mutations leading to dysregulation of innate immune response produce the expanding spectrum of monogenic autoinflammatory diseases (AIDs). They are characterized by seemingly unprovoked, recurrent episodes of systemic inflammation in wh
Autor:
Segundo, Bujan-Rivas, Maria, Basagaña, Francisca, Sena, Maria, Méndez, Maria Teresa, Dordal, Eva, Gonzalez-Roca, Estibaliz, Ruiz-Ortiz, Anna, Mensa-Vilaró, Susana, Plaza, Consuelo, Modesto, Josep, Ordi-Ros, Jordi, Yagüe, Ferrán, Martínez-Valle, Juan Ignacio, Aróstegui
Publikováno v:
Clinical and experimental rheumatology. 35(6)
Cryopyrin-associated periodic syndromes (CAPS) usually start during infancy as an urticarial-like rash and a marked acute phase response, with additional manifestations appearing during its evolution. The aim of this study was to expand the clinical
Publikováno v:
Medicina clinica. 139(8)