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Prognostic significance of FLT3 mutational status and expression levels in MLL-AF4+ and MLL-germline acute lymphoblastic leukemia.
Chillón MC, Gómez-Casares MT, López-Jorge CE, Rodriguez-Medina C, Molines A, Sarasquete ME, Alcoceba M, Miguel JD, Bueno C, Montes R, Ramos F, Rodríguez JN, Giraldo P, Ramírez M, García-Delgado R, Fuster JL, González-Díaz M, Menendez P. Chillón MC, et al. Leukemia. 2012 Nov;26(11):2360-6. doi: 10.1038/leu.2012.161. Epub 2012 Jun 18. Leukemia. 2012. PMID: 22705992
Wilms Tumor 1 gene expression levels improve risk stratification in AML patients. Results of a multicentre study within the Spanish Group for Molecular Biology in Haematology.
Martínez-Laperche C, Kwon M, Franco-Villegas AC, Chillón MC, Castro N, Anguita E, Dolz S, Rodríguez-Medina C, Hermosín L, Bellón JM, Prieto-Conde MI, Barragán E, Gómez-Casares M, Ayala R, Martínez-López J, González-Díaz M, Díez-Martin JL, Buño I; Cooperative Group for Molecular Biology in Haematology (GBMH). Martínez-Laperche C, et al. Br J Haematol. 2018 May;181(4):542-546. doi: 10.1111/bjh.14635. Epub 2017 Apr 3. Br J Haematol. 2018. PMID: 28369773 Free article. No abstract available.
Genomic analysis of a familial myelodysplasia/acute myeloid leukemia and inherited RUNX1 mutations without a pre-existing platelet disorder.
Prieto-Conde MI, Labrador J, Hermida G, Alonso S, Jiménez C, García-Álvarez M, Medina A, Balanzategui A, Alcoceba M, Sarasquete ME, Puig N, González V, Gutiérrez NC, García-Sanz R, González-Díaz M, Chillón MDC. Prieto-Conde MI, et al. Leuk Lymphoma. 2020 Jan;61(1):181-184. doi: 10.1080/10428194.2019.1648801. Epub 2019 Aug 6. Leuk Lymphoma. 2020. PMID: 31385734 No abstract available.
A New Next-Generation Sequencing Strategy for the Simultaneous Analysis of Mutations and Chromosomal Rearrangements at DNA Level in Acute Myeloid Leukemia Patients.
Prieto-Conde MI, Corchete LA, García-Álvarez M, Jiménez C, Medina A, Balanzategui A, Hernández-Ruano M, Maldonado R, Sarasquete ME, Alcoceba M, Puig N, González-Calle V, García-Sanz R, Gutiérrez NC, González-Díaz M, Chillón MC. Prieto-Conde MI, et al. J Mol Diagn. 2020 Jan;22(1):60-71. doi: 10.1016/j.jmoldx.2019.08.002. Epub 2019 Oct 9. J Mol Diagn. 2020. PMID: 31605801 Free article.
Reply to Brown et al: 'Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis'.
Prieto-Conde MI, Labrador J, Hermida G, Alonso S, Jiménez C, García-Alvarez M, Medina A, Balanzategui A, Alcoceba M, Sarasquete ME, Puig N, González V, Gutiérrez NC, García-Sanz R, González-Díaz M, Chillón MDC. Prieto-Conde MI, et al. Leuk Lymphoma. 2020 Jan;61(1):248-249. doi: 10.1080/10428194.2019.1680843. Epub 2019 Oct 23. Leuk Lymphoma. 2020. PMID: 31642380 No abstract available.
Identification of relapse-associated gene mutations by next-generation sequencing in low-risk acute myeloid leukaemia patients.
Prieto-Conde MI, Jiménez C, García-Álvarez M, Ramos F, Medina A, Cuello R, Balanzategui A, Alonso JM, Sarasquete ME, Queizán JA, Alcoceba M, Bárez A, Puig N, Cantalapiedra A, Gutiérrez NC, García-Sanz R, González-Díaz M, Chillón MC. Prieto-Conde MI, et al. Br J Haematol. 2020 May;189(4):718-730. doi: 10.1111/bjh.16420. Epub 2020 Mar 2. Br J Haematol. 2020. PMID: 32124426 Free article.
73 results