Mostrando resultados 37 a 48 de 48
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Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
openAccess | | 2015 | Panobinostat as part of induction and maintenance for elderly patients with newly diagnosed acute myeloid leukemia: phase Ib/II panobidara study | Ocio, Enrique M. CSIC ORCID ; Pérez-Simón, José A. CSIC ORCID; Chillón, M. del Carmen; Díez-Campelo, María; González, Marcos CSIC ORCID ; Vidriales, Maria Belén; Mateos, Maria Victoria; San Miguel, Jesús F. CSIC ORCID | artículo |
closedAccess | | 2017 | Prediction of peripheral neuropathy in multiple myeloma patients receiving bortezomib and thalidomide: a genetic study based on a single nucleotide polymorphism array | García-Sanz, Ramón; Corchete, Luis A.; Alcoceba, Miguel; Chillón, M. del Carmen; Jiménez, Cristina; Prieto-Conde, Isabel; García-Alvarez, María; Puig, Noemi; Rapado, Inmaculada; Barrio, Santiago; Oriol, Albert; Blanchard, María Jesús; Rubia, Javier de la; Martínez, Rafael; Lahuerta, Juan José; González, Marcos CSIC ORCID ; Mateos, Maria Victoria; San Miguel, Jesús F. CSIC ORCID; Martínez-López, Joaquín; Sarasquete, María Eugenia | artículo |
closedAccess | | 2017 | Quantitative PCR: an alternative approach to detect common copy number alterations in multiple myeloma | Chillón, M. del Carmen; Jiménez, Cristina; García-Sanz, Ramón; Alcoceba, Miguel; Prieto-Conde, Isabel; García-Alvarez, María; Antón, Alicia; Maldonado, Rebeca; Hernández-Ruano, Montserrat; González, Marcos CSIC ORCID ; Gutiérrez, Norma Carmen; Sarasquete, María Eugenia | artículo |
closedAccess | | 2020 | Reply to Brown et al: ‘Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis’ | Prieto-Conde, Isabel; Labrador, Jorge; Hermida, Gerardo; Alonso, Sara CSIC ORCID CVN; Jiménez, Cristina; García-Alvarez, María; Medina, Alejandro; Balanzategui, Ana; Alcoceba, Miguel; Sarasquete, María Eugenia; Puig, Noemi; González-Calle, Verónica; Gutiérrez, Norma Carmen; García-Sanz, Ramón; González, Marcos CSIC ORCID ; Chillón, M. del Carmen | carta al director |
openAccess | | 2012 | Risk of placenta-mediated pregnancy complications or pregnancy-related VTE in VTE-asymptomatic families of probands with VTE and heterozygosity for factor V Leiden or G20210 prothrombin mutation | Córdoba, Iris; Chillón, M. del Carmen; Sarasquete, María Eugenia; Martin-Herrero, Francisco; Guerrero Arroyo, María del Carmen CSIC ORCID ; Lozano, Francisco S.; González, Marcos CSIC ORCID ; González-Porras, José R. | artículo |
closedAccess | | 2012 | Simultaneous analysis of the expression of 14 genes with individual prognostic value in myelodysplastic syndrome patients at diagnosis: WT1 detection in peripheral blood adversely affects survival | Santamaría, Carlos; Cañizo, María Consuelo del; Díez-Campelo, María; Chillón, M. del Carmen; García-Sanz, Ramón; San Miguel, Jesús F. CSIC ORCID; González, Marcos CSIC ORCID | artículo |
openAccess | | 12-may-2023 | Supplementary material. Comparison of the 2022 and 2017 European LeukemiaNet risk classifications in a real-life cohort of the PETHEMA group | Sargas, Claudia; Ayala Bueno, Rosa CSIC ORCID; Larráyoz, María José; Chillón, M. del Carmen; Rodríguez-Arbolí, Eduardo CSIC ORCID; Bilbao, Cristina; Prados de la Torre, Esther; Martínez-Cuadrón, David; Rodríguez-Veiga, Rebeca; Boluda, Blanca; Gil, Cristina; Bernal, T.; Bergua, Juan; Algarra, Lorenzo; Tormo, Mar; Martínez-Sánchez, Pilar; Soria, Elena; Alonso-Domínguez, Juan Manuel; García, Raimundo; Amigo, María Luz; Herrera-Puente, Pilar; Sayas, María-José; Lavilla, Esperanza; Martínez-López, Joaquín; Calasanz, Mª Jose; García-Sanz, Ramón; Pérez-Simón, José A. CSIC ORCID; Gómez Casares, María T.; Sanchez-Garcia, Joaquin; Barragán, Eva; Montesinos, Pau | dataset |
closedAccess | | 2017 | The cryptic IRF2BP2-RARA fusion transforms hematopoietic stem/progenitor cells and induces retinoid-sensitive acute promyelocytic leukemia | Jovanovic, J. V.; Chillón, M. del Carmen; Vincent-Fabert, C.; Dillon, R.; Voisset, E.; Gutiérrez, Norma Carmen; Sanz, R. G.; Lopez, A. A. M.; Morgan, Y. G.; Lok, J.; Solomon, E.; Duprez, E.; Diáz, M. G.; Grimwade, D. | artículo |
closedAccess | | nov-2021 | The novel HLA-DQB1*06:03:27 allele characterised by sequence-based typing in a European bone marrow donor | Boix, Francisco; Chillón, M. del Carmen; García-Sánchez, S.; Alcoceba, Miguel; Marín-Rubio, Luis Alberto | artículo |
closedAccess | | 2015 | The predominant myeloma clone at diagnosis, CDR3 defined, is constantly detectable across all stages of disease evolution | Puig, Noemi; Sarasquete, María Eugenia; Balanzategui, Ana; Alcoceba, Miguel; Chillón, M. del Carmen; Sebastián, Elena; Gutiérrez, Norma Carmen; San Miguel, Jesús F. CSIC ORCID; García-Sanz, Ramón | artículo |
openAccess | | 2008 | The relevance of preferentially expressed antigen of melanoma (PRAME) as a marker of disease activity and prognosis in acute promyelocytic leukemia | Santamaría, Carlos; Chillón, M. del Carmen; García-Sanz, Ramón; Balanzategui, Ana; Sarasquete, María Eugenia; Alcoceba, Miguel; San Miguel, Jesús F. CSIC ORCID; González, Marcos CSIC ORCID | artículo |
closedAccess | | 2000 | Two new 3′ PML Breakpoints in t(15;17)(q22;q21)-positive acute promyelocytic leukemia | Chillón, M. del Carmen; González, Marcos CSIC ORCID ; García-Sanz, Ramón; Balanzategui, Ana; Mateos, Maria Victoria; Hernández, Jesús M. CSIC ORCID ; Orfao, Alberto CSIC ORCID ; San Miguel, Jesús F. CSIC ORCID | artículo |