Sanz MA - Search Results

1

De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.

Cigudosa JC, Odero MD, Calasanz MJ, Solé F, Salido M, Arranz E, Martínez-Ramirez A, Urioste M, Alvarez S, Cervera JV, MacGrogan D, Sanz MA, Nimer SD, Benitez J. Cigudosa JC, et al. Among authors: sanz ma. Genes Chromosomes Cancer. 2003 Apr;36(4):406-12. doi: 10.1002/gcc.10180. Genes Chromosomes Cancer. 2003. PMID: 12619165 Free article.

2

Identification of two atypical PML-RAR(alpha) transcripts in two patients with acute promyelocytic leukemia.

Barragán E, Bolufer P, Martín G, Cervera J, Moreno I, Capote FJ, Rosique P, Sanz MA. Barragán E, et al. Among authors: sanz ma. Leuk Res. 2002 May;26(5):439-42. doi: 10.1016/s0145-2126(01)00158-8. Leuk Res. 2002. PMID: 11916515

3

The t(4;22)(q12;q11) in atypical chronic myeloid leukaemia fuses BCR to PDGFRA.

Baxter EJ, Hochhaus A, Bolufer P, Reiter A, Fernandez JM, Senent L, Cervera J, Moscardo F, Sanz MA, Cross NC. Baxter EJ, et al. Among authors: sanz ma. Hum Mol Genet. 2002 Jun 1;11(12):1391-7. doi: 10.1093/hmg/11.12.1391. Hum Mol Genet. 2002. PMID: 12023981

4

Incidence and prognostic value of FLT3 internal tandem duplication and D835 mutations in acute myeloid leukemia.

Moreno I, Martín G, Bolufer P, Barragán E, Rueda E, Román J, Fernández P, León P, Mena A, Cervera J, Torres A, Sanz MA. Moreno I, et al. Among authors: sanz ma. Haematologica. 2003 Jan;88(1):19-24. Haematologica. 2003. PMID: 12551822

5

A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia.

García-Casado Z, Cervera J, Valencia A, Pajuelo JC, Mena-Duran AV, Barragán E, Bolufer P, Sanz MA. García-Casado Z, et al. Among authors: sanz ma. Cancer Genet Cytogenet. 2006 Jul 1;168(1):73-6. doi: 10.1016/j.cancergencyto.2005.12.014. Cancer Genet Cytogenet. 2006. PMID: 16772124

6

High-level amplification of the RUNX1 gene in two cases of childhood acute lymphoblastic leukemia.

García-Casado Z, Cervera J, Verdeguer A, Tasso M, Valencia A, Pajuelo JC, Mena-Duran AV, Barragán E, Blanes M, Bolufer P, Sanz MA. García-Casado Z, et al. Among authors: sanz ma. Cancer Genet Cytogenet. 2006 Oct 15;170(2):171-4. doi: 10.1016/j.cancergencyto.2006.05.011. Cancer Genet Cytogenet. 2006. PMID: 17011991

7

Influence of genetic polymorphisms on the risk of developing leukemia and on disease progression.

Bolufer P, Barragan E, Collado M, Cervera J, López JA, Sanz MA. Bolufer P, et al. Among authors: sanz ma. Leuk Res. 2006 Dec;30(12):1471-91. doi: 10.1016/j.leukres.2006.01.016. Epub 2006 Oct 4. Leuk Res. 2006. PMID: 17023046 Review.

8

The GST deletions and NQO1*2 polymorphism confers interindividual variability of response to treatment in patients with acute myeloid leukemia.

Barragan E, Collado M, Cervera J, Martin G, Bolufer P, Roman J, Sanz MA. Barragan E, et al. Among authors: sanz ma. Leuk Res. 2007 Jul;31(7):947-53. doi: 10.1016/j.leukres.2006.10.002. Epub 2006 Nov 21. Leuk Res. 2007. PMID: 17118447

9

The potential effect of gender in combination with common genetic polymorphisms of drug-metabolizing enzymes on the risk of developing acute leukemia.

Bolufer P, Collado M, Barragán E, Cervera J, Calasanz MJ, Colomer D, Roman-Gómez J, Sanz MA. Bolufer P, et al. Among authors: sanz ma. Haematologica. 2007 Mar;92(3):308-14. doi: 10.3324/haematol.10752. Haematologica. 2007. PMID: 17339179 Free article.

10

MLL amplification in acute myeloid leukemia.

Pajuelo-Gámez JC, Cervera J, García-Casado Z, Mena-Durán AV, Valencia A, Barragán E, Such E, Bolufer P, Sanz MA. Pajuelo-Gámez JC, et al. Among authors: sanz ma. Cancer Genet Cytogenet. 2007 Apr 15;174(2):127-31. doi: 10.1016/j.cancergencyto.2006.11.019. Cancer Genet Cytogenet. 2007. PMID: 17452254

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