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Page 1
Negative impact on clinical outcome of the mutational co-occurrence of SF3B1 and DNMT3A in refractory anemia with ring sideroblasts (RARS).
Martín I, Such E, Navarro B, Vicente A, López-Pavía M, Ibáñez M, Tormo M, Villamón E, Gómez-Seguí I, Luna I, Oltra S, Pedrola L, Sanz MA, Cervera J, Sanz G. Martín I, et al. Among authors: oltra s. Leuk Lymphoma. 2017 Jul;58(7):1686-1693. doi: 10.1080/10428194.2016.1246725. Epub 2016 Oct 24. Leuk Lymphoma. 2017. PMID: 27771989
WT1 isoform expression pattern in acute myeloid leukemia.
Luna I, Such E, Cervera J, Barragán E, Ibañez M, Gómez-Seguí I, López-Pavía M, Llop M, Fuster O, Dolz S, Oltra S, Alonso C, Vera B, Lorenzo I, Martínez-Cuadrón D, Montesinos P, Senent ML, Moscardó F, Bolufer P, Sanz MA. Luna I, et al. Among authors: oltra s. Leuk Res. 2013 Dec;37(12):1744-9. doi: 10.1016/j.leukres.2013.10.009. Epub 2013 Oct 22. Leuk Res. 2013. PMID: 24211094
Rapid screening of ASXL1, IDH1, IDH2, and c-CBL mutations in de novo acute myeloid leukemia by high-resolution melting.
Ibáñez M, Such E, Cervera J, Luna I, Gómez-Seguí I, López-Pavía M, Dolz S, Barragán E, Fuster O, Llop M, Rodríguez-Veiga R, Avaria A, Oltra S, Senent ML, Moscardó F, Montesinos P, Martínez-Cuadrón D, Martín G, Sanz MA. Ibáñez M, et al. Among authors: oltra s. J Mol Diagn. 2012 Nov;14(6):594-601. doi: 10.1016/j.jmoldx.2012.06.006. Epub 2012 Aug 25. J Mol Diagn. 2012. PMID: 22929312 Free article.
Analysis of SNP rs16754 of WT1 gene in a series of de novo acute myeloid leukemia patients.
Luna I, Such E, Cervera J, Barragán E, Jiménez-Velasco A, Dolz S, Ibáñez M, Gómez-Seguí I, López-Pavía M, Llop M, Fuster Ó, Oltra S, Moscardó F, Martínez-Cuadrón D, Senent ML, Gascón A, Montesinos P, Martín G, Bolufer P, Sanz MA. Luna I, et al. Among authors: oltra s. Ann Hematol. 2012 Dec;91(12):1845-53. doi: 10.1007/s00277-012-1596-x. Epub 2012 Oct 16. Ann Hematol. 2012. PMID: 23070125
MAGE-A1 expression is associated with good prognosis in neuroblastoma tumors.
Grau E, Oltra S, Martínez F, Orellana C, Cañete A, Fernández JM, Hernández-Martí M, Castel V. Grau E, et al. Among authors: oltra s. J Cancer Res Clin Oncol. 2009 Apr;135(4):523-31. doi: 10.1007/s00432-008-0484-1. Epub 2008 Sep 27. J Cancer Res Clin Oncol. 2009. PMID: 18820946
Prenatal study of common submicroscopic "genomic disorders" using MLPA with subtelomeric/microdeletion syndrome probe mixes, among gestations with ultrasound abnormalities in the first trimester.
Roselló M, Ferrer-Bolufer I, Monfort S, Oltra S, Quiroga R, Martínez F, Gonzalvo M, Benac A, Perales A, Orellana C. Roselló M, et al. Among authors: oltra s. Eur J Med Genet. 2010 Mar-Apr;53(2):76-9. doi: 10.1016/j.ejmg.2009.12.003. Epub 2009 Dec 29. Eur J Med Genet. 2010. PMID: 20004752
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