Zobrazeno 1 - 10
of 31
pro vyhledávání: '"José P. Dapena"'
Autor:
Celia Moreno, Eduardo Ramos-Elbal, Pablo Velasco, Yurena Aguilar, Berta Gonzáález Martínez, Carolina Fuentes, Águeda Molinos, Pilar Guerra-García, Pilar Palomo, Jaime Verdu, Rosa María Adán Pedroso, José Manuel Vagace, Mónica López-Duarte, Alexandra Regueiro, María Tasso, José Luis Dapena, José Antonio Salinas, Samuel Navarro, Francisco Bautista, Álvaro Lassaletta, Francisco Lendínez, Susana Rives, Antonia Pascual, Antonia Rodríguez, José María Pérez-Hurtado, José María Fernández, Antonio Pérez-Martínez, Marta González-Vicent, Cristina Díaz de Heredia, José Luis Fuster
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionStudies addressing the role of haploidentical as alternative to HLA-matched donors for stem cell transplantation (SCT) often include patients with diverse hematological malignancies in different remission statuses.MethodsWe compared outco
Externí odkaz:
https://doaj.org/article/7dbf7432b2ec48bcadbf116e3c7b2bf9
Autor:
Paula Gebellí Jové, Nazaret Sánchez Sierra, Ana Sangrós Gimenez, José Luis Dapena Díaz, Nuria Conde Cuevas
Publikováno v:
Anales de Pediatría, Vol 97, Iss 6, Pp 429-430 (2022)
Externí odkaz:
https://doaj.org/article/138b64ac03e9427b86c32aa24da0222c
Autor:
Clara Vicente-Garcés, Elena Esperanza-Cebollada, Sara Montesdeoca, Montserrat Torrebadell, Susana Rives, José Luis Dapena, Albert Català, Nuria Conde, Mireia Camós, Nerea Vega-García
Publikováno v:
Frontiers in Molecular Biosciences, Vol 9 (2022)
Development of next-generation sequencing (NGS) has provided useful genetic information to redefine diagnostic, prognostic, and therapeutic strategies for the management of acute leukemia (AL). However, the application in the clinical setting is stil
Externí odkaz:
https://doaj.org/article/e821a06a15d34238a5df1afa070e0763
Autor:
Laura Viñas-Giménez, Rafael Rincón, Roger Colobran, Xavier de la Cruz, Verónica Paola Celis, José Luis Dapena, Laia Alsina, Joan Sayós, Mónica Martínez-Gallo
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory disorder. HLH can be considered as a threshold disease depending on the trigger and the residual NK-cell cytotoxicity. In this study, we analyzed the molecular and funct
Externí odkaz:
https://doaj.org/article/adad2843b85d4f1691acf851788361af
Autor:
Nerea Vega-García, Sara Perez-Jaume, Elena Esperanza-Cebollada, Clara Vicente-Garcés, Montserrat Torrebadell, Antonio Jiménez-Velasco, Margarita Ortega, Marta Llop, Lorea Abad, José Manuel Vagace, Alfredo Minguela, Marta Pratcorona, Joaquín Sánchez-Garcia, Clara B. García-Calderón, María Teresa Gómez-Casares, Estela Martín-Clavero, Adela Escudero, Marta Riñón Martinez-Gallo, Luz Muñoz, María Rosario Velasco, Marina García-Morin, Albert Català, Antonia Pascual, Pablo Velasco, José Mª. Fernández, Alvaro Lassaletta, José Luis Fuster, Isabel Badell, Águeda Molinos-Quintana, Antonio Molinés, Pilar Guerra-García, Antonio Pérez-Martínez, Miriam García-Abós, Reyes Robles Ortiz, Sandra Pisa, Rosa Adán, Cristina Díaz de Heredia, José Luis Dapena, Susana Rives, Manuel Ramírez-Orellana, Mireia Camós
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Robust and applicable risk-stratifying genetic factors at diagnosis in pediatric T-cell acute lymphoblastic leukemia (T-ALL) are still lacking, and most protocols rely on measurable residual disease (MRD) assessment. In our study, we aimed to analyze
Externí odkaz:
https://doaj.org/article/76d44086f8a049c3816cf6758487be24
Autor:
Emilio Monteagudo, Itziar Astigarraga, Áurea Cervera, María Angeles Dasí, Ana Sastre, Rubén Berrueco, José Luis Dapena
Publikováno v:
Anales de Pediatría, Vol 91, Iss 2, Pp 127.e1-127.e10 (2019)
Resumen: La trombocitopenia inmune primaria, anteriormente conocida como púrpura trombocitopénica inmune, es una enfermedad cuyo manejo diagnóstico y terapéutico ha sido siempre controvertido. La Sociedad Española de Hematología y Oncología Pe
Externí odkaz:
https://doaj.org/article/f46c7b3158284b6395ecbf461a0189a0
Autor:
Emilio Monteagudo, Itziar Astigarraga, Áurea Cervera, María Angeles Dasí, Ana Sastre, Rubén Berrueco, José Luis Dapena
Publikováno v:
Anales de Pediatría (English Edition), Vol 91, Iss 2, Pp 127.e1-127.e10 (2019)
Primary immune thrombocytopenia, formerly known as immune thrombocytopenic purpura, is a disease for which the clinical and therapeutic management has always been controversial. The ITP working group of the Spanish Society of Paediatric Haematology a
Externí odkaz:
https://doaj.org/article/2d7e1390fdd34e4fb991946fe1708244
Publikováno v:
Anales de Pediatría, Vol 89, Iss 3, Pp 189.e1-189.e8 (2018)
Resumen: La trombocitopenia inmune (PTI) es una entidad relativamente frecuente en pediatría. Aunque su evolución suele ser favorable en la mayoría de los casos, el manejo de aquellos pacientes en los que la enfermedad persiste es muy controvertid
Externí odkaz:
https://doaj.org/article/478feb8957a7454a88a8e1de9c751ad4
Publikováno v:
Anales de Pediatría (English Edition), Vol 89, Iss 3, Pp 189.e1-189.e8 (2018)
Immune thrombocytopaenia (ITP) is a relatively common disorder in childhood. Although it usually achieves spontaneous remission at this age, the management of persistent or chronic ITP in children is still controversial. The aim of this article is to
Externí odkaz:
https://doaj.org/article/e211792328fc457dbca5b797f4bc86c6
Publikováno v:
SSRN Electronic Journal.
Greed and fear are the main psychological factors driving investment deci-sions, and the VIX Index is regarded as the most important measure of howfearful the market feels about future returns of the main equity index, theS&P 500 Index. However, give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6afb479dadd4fb52f66aa9873c87954
https://doi.org/10.2139/ssrn.3806521
https://doi.org/10.2139/ssrn.3806521