Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Eva Galvez"'
Autor:
Nuria Revilla, Javier Corral, Antonia Miñano, Maria Eva Mingot-Castellano, Rosa Maria Campos, Francisco Velasco, Nicolas Gonzalez, Eva Galvez, Ruben Berrueco, Inmaculada Fuentes, Tomas Jose Gonzalez-Lopez, Maria Eugenia de la Morena-Barrio, Jose Ramon Gonzalez-Porras, Vicente Vicente, Maria Luisa Lozano
Publikováno v:
Platelets, Vol 30, Iss 6, Pp 743-751 (2019)
Patients with multirefractory immune thrombocytopenia (ITP) have limited treatment options. Recent data suggest that specific anti-platelet antibodies may cause destruction of platelets by favoring platelet loss of sialic acid. In this multicenter st
Externí odkaz:
https://doaj.org/article/57233faa030a4575914a71110afa3819
Autor:
Elena G. Arias-Salgado, Eva Galvez, Lurdes Planas-Cerezales, Laura Pintado-Berninches, Elena Vallespin, Pilar Martinez, Jaime Carrillo, Laura Iarriccio, Anna Ruiz-Llobet, Albert Catalá, Isabel Badell-Serra, Luis I. Gonzalez-Granado, Andrea Martín-Nalda, Mónica Martínez-Gallo, Ana Galera-Miñarro, Carmen Rodríguez-Vigil, Mariana Bastos-Oreiro, Guiomar Perez de Nanclares, Virginia Leiro-Fernández, Maria-Luz Uria, Cristina Diaz-Heredia, Claudia Valenzuela, Sara Martín, Belén López-Muñiz, Pablo Lapunzina, Julian Sevilla, María Molina-Molina, Rosario Perona, Leandro Sastre
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract Background Telomeres are nucleoprotein structures present at the terminal region of the chromosomes. Mutations in genes coding for proteins involved in telomere maintenance are causative of a number of disorders known as telomeropathies. The
Externí odkaz:
https://doaj.org/article/2395ce84c653431ab41d130f9737dfc8
Autor:
Miguel A. Diaz, Josune Zubicaray, Blanca Molina, Lorea Abad, Ana Castillo, Elena Sebastian, Eva Galvez, Julia Ruiz, Jose Luis Vicario, Manuel Ramirez, Julian Sevilla, Marta González-Vicent
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
We prospectively analyzed outcomes of haploidentical hematopoietic stem cell transplantation using αβ+ T-cell receptor/CD19+ depleted grafts. Sixty-three transplantations were performed in 60 patients. Twenty-eight patients were diagnosed with acut
Externí odkaz:
https://doaj.org/article/63dbdb2b47834264b5c00a86ec288100
Autor:
Josune Zubicaray, Maria Ivanova, June Iriondo, Jorge García Martínez, Rafael Muñoz-Viana, Lorea Abad, Lorena García-García, Jesús González de Pablo, Eva Gálvez, Elena Sebastián, Manuel Ramírez, Luis Madero, Miguel Ángel Díaz, África González-Murillo, Julián Sevilla
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
IntroductionFanconi anemia (FA) is an inherited disorder characterized by bone marrow failure, congenital malformations, and predisposition to malignancies. Alterations in hematopoietic stem cells (HSC) have been reported, but little is known regardi
Externí odkaz:
https://doaj.org/article/a1912601287e4b89a684e68a105b628e
Autor:
Josune, Zubicaray, Eva, Galvez, Elena, Sebastian, Blanca, Molina, Marta, González-Vicent, Ana, Castillo, Manuel, Ramírez, Luis, Madero, Miguel Angel, Díaz, Julian, Sevilla
Publikováno v:
Journal of clinical apheresisREFERENCES. 36(1)
In order to propose risk-adapted mobilization algorithms, several authors have tried to look for predictive factors of the CD34We report the results of 46 mobilizations and apheresis procedures performed in our center with unfavorable D/R ratio. Mobi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ac838cee3f642d70ba93d2a8e7aebb9
https://pubmed.ncbi.nlm.nih.gov/33079424
https://pubmed.ncbi.nlm.nih.gov/33079424
Autor:
Francisco Velasco, Eva Galvez, Tomás José González-López, Rubén Berrueco, Nicolas Gonzalez, Inmaculada Fuentes, Maria Eva Mingot-Castellano, Vicente Vicente, Maria Eugenia de la Morena-Barrio, Rosa Campos, José Ramón González-Porras, Nuria Revilla, Antonia Miñano, Maria Luisa Lozano, Javier Corral
Publikováno v:
Platelets. 30:743-751
Patients with multirefractory immune thrombocytopenia (ITP) have limited treatment options. Recent data suggest that specific anti-platelet antibodies may cause destruction of platelets by favoring platelet loss of sialic acid. In this multicenter st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e653d2981cf9f94eced5242eaa8245be
https://doi.org/10.1080/09537104.2018.1513476
https://doi.org/10.1080/09537104.2018.1513476
Autor:
Josune Zubicaray, Sofía Martin-Consuegra, Monserrat Nieto, Gustavo Albi, June Iriondo, Elena Sebastian, Eva Gálvez, Blanca Molina, Marta González-Vicent, Jesus Gonzalez de Pablo, Ana Castillo, Manuel Ramírez, Luis Madero, Miguel Angel Díaz, Julián Sevilla
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionThe use of peripheral blood progenitor cells (PBPCs) as a source for hematopoietic stem cell transplantation (HSCT) in pediatric healthy donors is still under debate. The risk of a central venous catheter (CVC) placement and catheter-rela
Externí odkaz:
https://doaj.org/article/d50be8dcf4db4eaa802ca15d15d11cea
Autor:
Julián Sevilla, Susana Navarro, Paula Rio, Rebeca Sánchez-Domínguez, Josune Zubicaray, Eva Gálvez, Eva Merino, Elena Sebastián, Carmen Azqueta, José A. Casado, José C. Segovia, Omaira Alberquilla, Massimo Bogliolo, Francisco J. Román-Rodríguez, Yari Giménez, Lise Larcher, Rocío Salgado, Roser M. Pujol, Raquel Hladun, Ana Castillo, Jean Soulier, Sergi Querol, Jesús Fernández, Jonathan Schwartz, Nagore García de Andoín, Ricardo López, Albert Catalá, Jordi Surralles, Cristina Díaz-de-Heredia, Juan A. Bueren
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss , Pp 66-75 (2021)
Difficulties in the collection of hematopoietic stem and progenitor cells (HSPCs) from Fanconi anemia (FA) patients have limited the gene therapy in this disease. We have investigated (ClinicalTrials.gov, NCT02931071) the safety and efficacy of filgr
Externí odkaz:
https://doaj.org/article/ff619351134c4b8d89b9a48f91e2e8e9
Autor:
Sandra Fernández-Plaza, Jesús González de Pablo, Eva Gálvez, Josune Zubicaray, Julián Sevilla, Elena Sebastián
Publikováno v:
Anales de Pediatría, Vol 95, Iss 2, Pp 86-92 (2021)
Resumen: Introducción: En los últimos años se han experimentado cambios en el manejo de los pacientes con trombocitopenia inmune primaria. En este estudio se revisan las características de los pacientes con trombocitopenia inmune primaria del Hos
Externí odkaz:
https://doaj.org/article/b17001ac87c246b491cfb12b1e450c3b
Autor:
Sandra Fernández-Plaza, Jesús González de Pablo, Eva Gálvez, Josune Zubicaray, Julián Sevilla, Elena Sebastián
Publikováno v:
Anales de Pediatría (English Edition), Vol 95, Iss 2, Pp 86-92 (2021)
Introduction: In recent years, there have been changes in the management of patients with primary immune thrombocytopenia. In this study, a review is presented of the characteristics and outcomes of children with primary immune thrombocytopenia in a
Externí odkaz:
https://doaj.org/article/cc12e7657bec47589561f9cb3a02c5be