Repositorio Dspace

Listar por autor "Badell, Isabel"

Listar por autor "Badell, Isabel"

Ordenar por:Orden:Resultados:

  • Measurable Residual Disease Assessed by Flow-Cytometry Is a Stable Prognostic Factor for Pediatric T-Cell Acute Lymphoblastic Leukemia in Consecutive SEHOP Protocols Whereas the Impact of Oncogenetics Depends on Treatment 
    Vega-García, Nerea; Pérez-Jaume, Sara; Esperanza-Cebollada, Elena; Vicente-Garces, Clara; Torrebadell, Montserrat; Jiménez-Velasco, Antonio; Ortega, Margarita; Llop, Marta; Abad, Lorea; Vagace, José-Manuel; Minguela-Puras, Alfredo; Pratcorona, Marta; Sánchez-García, Joaquín; García-Calderón, Clara-B; Gómez-Casares, María-Teresa; Martín-Clavero, Estela; Escudero, Adela; Rinon-Martínez-Gallo, Marta; Muñoz, Luz; Rosario-Velasco, María; García-Morin, Marina; Catala, Albert; Pascual, Antonia; Velasco, Pablo; Fernández, José-María; Lassaletta, Álvaro; Fuster, José-Luis; Badell, Isabel; Molinos-Quintana, Agueda; Molines, Antonio; Guerra-García, Pilar; Pérez-Martínez, Antonio; García-Abos, Miriam; Robles-Ortiz, Reyes; Pisa, Sandra; Adan, Rosa; Díaz-de-Heredia, Cristina; Dapena, José-Luis; Rives, Susana; Ramírez-Orellana, Manuel; Camos, Mireia (FRONTIERS MEDIA SA, 2021-02)
    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 ...
  • Next-generation Sequencing in Bone Marrow Failure Syndromes and Isolated Cytopenias: Experience of the Spanish Network on Bone Marrow Failure Syndromes 
    Gálvez, Eva; Vallespín, Elena; Arias-Salgado, Elena-G; Sánchez-Valdepenas, Carmen; Giménez, Yari; Navarro, Susana; Rio, Paula; Bogliolo, Massimo; Pujol, Roser; Peiro, Montserrat; Nevado, Julián; Zubicaray, Josune; Sebastian, Elena; Catala, Albert; Beléndez, Cristina; Díaz-de-Heredia, Cristina; Galera, Ana; Badell, Isabel; Madero, Luis; Perona, Rosario; Sastre, Leandro; Surralles, Jordi; Bueren, Juan; Lapunzina, Pablo; Sevilla, Julián (LIPPINCOTT WILLIAMS & WILKINS, 2021-04)
    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 ...
  • Prognostic significance of mutation type and chromosome fragility in Fanconi anemia 
    Jose-Ramírez, María; Pujol, Roser; Minguillon, Jordi; Bogliolo, Massimo; Persico, Ilaria; Cavero, Debora; de-la-Cal, Aurora; Rio, Paula; Navarro, Susana; Casado, José-Antonio; Bailador, Almudena; Sánchez-de-la-Fuente, Antonio; López-de-Heredia, Miguel; Almazan, Francisco; Antelo, María-Luisa; Argiles, Bienvenida; Badell, Isabel; Baragano, Marta; Belendez, Cristina; Bermudez-Cortés, Mar; Bernues, Marta; Isabel-Buedo, María; Carrasco, Estela; Catalá, Albert; Costa, Dolors; Cuesta, Isabel; Fernández-Delgado, Rafael; Fernández-Teijeir, Ana; Figuera, Ángela; García, Marta; Gondra, Ainhoa; González, Macarena; González-Muñiz, Soledad; Hernández-Rodríguez, Inés; Ibáñez, Fátima; John-Kelleher, Nicholas; Lendinez, Francisco; López, Mónica; López-Almaraz, Ricardo; Marchante, Inmaculada; Mendoza, Carmen; Nieto, José; Ojeda, Emilio; Payan-Pernia, Salvador; Peláez, Irene; Pérez-de-Soto, Inmaculada; Portugal, Raquel; Ramos-Arroyo, María-A; Regueiro, Alexandra; Rodríguez, Ana; Rosell, Jordi; Sáez, Raquel; Sánchez, José; Sánchez, Martha; Leónor-Senent, Ma; Tapia, María; Trujillo-Quintero, Juan-Pablo; Manuel-Vagace, José; Verdu-Amoros, Jaime; Verdugo, Victoria; Vidales, Isabel; Villarreal, Jasson; Díaz-de-Heredia, Cristina; Sevilla, Julián; Bueren, Juan-Antonio; Surralles, Jordi (WILEY, 2025-02)
    Fanconi anemia (FA) is a rare genetic disease characterized by high phenotypic and genotypic heterogeneity, and extreme chromosome fragility. To better understand the natural history of FA, identify genetic risk and ...