Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Cristina Díaz De Heredia"'
Autor:
Oskar Marin-Bejar, Damia Romero-Moya, Javier Rodriguez-Ubreva, Maximiliano Distefano, Francesca Lessi, Paolo Aretini, Alessandro Liquori, Julio Castaño, Emilia Kozyra, Lili Kotmayer, Clara Bueno, José Cervera, José Carlos Rodriguez-Gallego, Josep F Nomdedeu, Laura Murillo-Sanjuán, Cristina Díaz de Heredia, Antonio Pérez-Martinez, Félix López-Cardenas, Carolina Martínez-Laperche, Nieves Dorado-Herrero, Francisco M Marco, Felipe Prósper, Pablo Menendez, David Valcárcel, Esteban Ballestar, Csaba Bödör, Anna Bigas, Albert Catalá, Marcin W Wlodarski, Alessandra Giorgetti
Publikováno v:
HemaSphere, Vol 7, p e891194b (2023)
Externí odkaz:
https://doaj.org/article/73cdfb6289c94ebfa4e147d1498cc8f1
Autor:
Víctor Galán Gómez, Lydia de la Fuente Regaño, Antonia Rodríguez Villa, Cristina Díaz de Heredia Rubio, Marta González Vicent, Isabel Badell Serra, José María Fernández, Antonia Isabel Pascual Martínez, José María Pérez Hurtado, Mónica López Duarte, M. Soledad Maldonado Regalado, Antonio Pérez-Martínez
Publikováno v:
Anales de Pediatría, Vol 96, Iss 4, Pp 309-318 (2022)
Resumen: Introducción: Los resultados de los pacientes con diagnóstico de leucemia linfoblástica aguda con cromosoma de Philadelphia (LLA-Ph) continúan siendo desfavorables comparados con los otros tipos de leucemias linfoblásticas agudas, pese
Externí odkaz:
https://doaj.org/article/bdda080b600643dba7d292b46f92f34c
Autor:
Víctor Galán Gómez, Lydia de la Fuente Regaño, Antonia Rodríguez Villa, Cristina Díaz de Heredia Rubio, Marta González Vicent, Isabel Badell Serra, José María Fernández, Antonia Isabel Pascual Martínez, José María Pérez Hurtado, Mónica López Duarte, M. Soledad Maldonado Regalado, Antonio Pérez-Martínez
Publikováno v:
Anales de Pediatría (English Edition), Vol 96, Iss 4, Pp 309-318 (2022)
Introduction: Outcomes in patients diagnosed of acute lymphoblastic leukemia with Philadelphia chromosome (Ph-ALL) remains unfavourable compared to other subtypes of acute lymphoblastic leukemia despite improvements in drug treatments as well as adva
Externí odkaz:
https://doaj.org/article/44dbbc0fb46e4deaba279d31c18bd634
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:
Oskar Marin-Bejar, Damia Romero-Moya, Javier Rodriguez-Ubreva, Maximiliano Distefano, Francesca Lessi, Paolo Aretini, Alessandro Liquori, Julio Castaño, Emilia Kozyra, Lili Kotmayer, Clara Bueno, José Cervera, José Carlos Rodriguez-Gallego, Josep F Nomdedeu, Laura Murillo-Sanjuán, Cristina Díaz de Heredia, Antonio Pérez-Martinez, Félix López-Cadenas, Carolina Martínez-Laperche, Nieves Dorado-Herrero, Francisco M Marco, Felipe Prósper, Pablo Menendez, David Valcárcel, Esteban Ballestar, Csaba Bödör, Anna Bigas, Albert Catalá, Marcin W Wlodarski, Alessandra Giorgetti
Publikováno v:
Haematologica, Vol 108, Iss 9 (2023)
Externí odkaz:
https://doaj.org/article/64a9f674d5c1431a8af78aa2de7d0937
Autor:
José A. Casado, Antonio Valeri, Rebeca Sanchez-Domínguez, Paula Vela, Andrea López, Susana Navarro, Omaira Alberquilla, Helmut Hanenberg, Roser Pujol, José-Carlos Segovia, Jordi Minguillón, Jordi Surrallés, Cristina Díaz de Heredia, Julián Sevilla, Paula Rio, Juan A. Bueren
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 15 (2022)
Fanconi anemia (FA) is the most prevalent inherited bone marrow failure (BMF) syndrome. Nevertheless, the pathophysiological mechanisms of BMF in FA have not been fully elucidated. Since FA cells are defective in DNA repair, we hypothesized that FA h
Externí odkaz:
https://doaj.org/article/7a971dce26ce4b9da8072027a4e7901d
Autor:
Eva Gálvez, Elena Vallespín, Elena G. Arias-Salgado, Carmen Sánchez-Valdepeñas, Yari Giménez, Susana Navarro, Paula Río, Massimo Bogliolo, Roser Pujol, Montserrat Peiró, Julián Nevado, Josune Zubicaray, Elena Sebastián, Albert Catalá, Cristina Beléndez, Cristina Díaz de Heredia, Ana Galera, Isabel Badell, Luis Madero, Rosario Perona, Leandro Sastre, Jordi Surrallés, Juan Bueren, Pablo Lapunzina, Julián Sevilla
Publikováno v:
HemaSphere, Vol 5, Iss 4, p e539 (2021)
Inherited bone marrow failure syndromes (IBMFSs) are a group of congenital rare diseases characterized by bone marrow failure, congenital anomalies, high genetic heterogeneity, and predisposition to cancer. Appropriate treatment and cancer surveillan
Externí odkaz:
https://doaj.org/article/7171cad4d97c4e6b9d227d6066cf270c
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:
Valeria Rizzuto, Tamara T. Koopmann, Adoración Blanco-Álvarez, Barbara Tazón-Vega, Amira Idrizovic, Cristina Díaz de Heredia, Rafael Del Orbe, Miriam Vara Pampliega, Pablo Velasco, David Beneitez, Gijs W. E. Santen, Quinten Waisfisz, Mariet Elting, Frans J. W. Smiers, Anne J. de Pagter, Jean-Louis H. Kerkhoffs, Cornelis L. Harteveld, Maria del Mar Mañú-Pereira
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglobin (Hb) variants with decreased stability. UHs are therefore easily precipitating, causing hemolysis and, in some cases, leading to dominant beta-tha
Externí odkaz:
https://doaj.org/article/ccdae50896004ad484f211a23535bb0c
Autor:
Lucía López-Granados, Montserrat Torrent, Ana Sastre, Marta Gonzalez-Vicent, Cristina Díaz de Heredia, Bienvenida Argilés, Antonia Pascual, José M. Pérez-Hurtado, Luisa Sisinni, Miguel Ángel Diaz, Izaskun Elorza, M. Angeles Dasí, Isabel Badell
Publikováno v:
Anales de Pediatría, Vol 88, Iss 4, Pp 196-203 (2018)
Resumen: Introducción: El trasplante de progenitores hematopoyéticos (TPH) consiste en implantar elementos celulares capaces de generar un sistema hematopoyético nuevo y sano. El régimen de intensidad reducida (RIR) consiste en un tratamiento pre
Externí odkaz:
https://doaj.org/article/80b416e57d994fbdb55e85657e43c69b