Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Josune, Zubicaray"'
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionFanconi anemia (FA) is a genomic instability disorder associated with congenital abnormalities, including short stature and the presence of central nervous system anomalies, especially in the hypothalamic-pituitary area. Thus, differences
Externí odkaz:
https://doaj.org/article/49bbf2bcbebf4137919fcb855d853ccd
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, Ana Gomez, June Iriondo, Reyes Gimenez, Lorea Abad, Carmen Matasans, Elena Sebastian, Alejandro Sanz, Jesus Gonzalez De Pablo, Manuel Ramirez, Julian Sevilla
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100056- (2023)
Externí odkaz:
https://doaj.org/article/7af96644581442f6a2c14ea713778cd9
Autor:
Miren Lasaga, Paula Río, Amaia Vilas-Zornoza, Nuria Planell, Susana Navarro, Diego Alignani, Beatriz Fernández-Varas, Daniel Mouzo, Josune Zubicaray, Roser M. Pujol, Eileen Nicoletti, Jonathan D. Schwartz, Julián Sevilla, Marina Ainciburi, Asier Ullate-Agote, Jordi Surrallés, Rosario Perona, Leandro Sastre, Felipe Prosper, David Gomez-Cabrero, Juan A. Bueren
Publikováno v:
Haematologica, Vol 108, Iss 10 (2023)
Clinical trials have shown that lentiviral-mediated gene therapy can ameliorate bone marrow failure (BMF) in nonconditioned Fanconi anemia (FA) patients resulting from the proliferative advantage of corrected FA hematopoietic stem and progenitor cell
Externí odkaz:
https://doaj.org/article/d53a95898f024aef96171022924acc08
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
Publikováno v:
Anales de Pediatría, Vol 94, Iss 4, Pp 206-212 (2021)
Resumen: Introducción: La anemia hemolítica autoinmune (AHAI) es una enfermedad rara en niños, generalmente autolimitada. Material y métodos: Estudio descriptivo transversal en menores de 18 años diagnosticados de AHAI desde enero de 1997 a juli
Externí odkaz:
https://doaj.org/article/29819933b1f447d18c78e1088eb5b280
Publikováno v:
Anales de Pediatría (English Edition), Vol 94, Iss 4, Pp 206-212 (2021)
Introduction: Autoimmune hemolytic anemia (AIHA) is a rare and generally self-limiting disease in children. Material and methods: A descriptive cross-sectional study was performed in children under 18 years diagnosed with AIHA from January 1997 to Ju
Externí odkaz:
https://doaj.org/article/20eb2d7601704d96a37b6c6812a44408