16 results on '"Eclache, Virginie"'
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2. Détection du chromosome Philadelphie chez les patients atteints de leucémie myéloïde chronique: Places respectives de la cytogénétique de l'hybridation in situ en fluorescence et de l'analyse moléculaire par RT-PCR
3. Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL1 or BCR deletion status or response to imatinib therapy
4. A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation
5. Cryptic deletion involving the ATM locus at 11q22.3∼q23.1 in B-cell chronic lymphocytic leukemia and related disorders
6. A constitutional translocation t(1;4)(p21;p15) in a case of chronic lymphocytic leukemia
7. TP53, XPO1 and ATM Mutations Exclusive Distribution in the Adverse Prognosis Chronic Lymphocytic Leukemia (CLL) Group.
8. High Frequency of Mutations in BTK and PLCG2 in Chronic Lymphocytic Leukemia (CLL) Patients on Ibrutinib Therapy.
9. Occurrence of myelodysplastic syndrome in 2 patients with reticular dysgenesis.
10. Impact of baseline cytogenetic findings and cytogenetic response on outcome of high-risk myelodysplastic syndromes and low blast count AML treated with azacitidine.
11. Prognostic value of TP53 gene mutations in myelodysplastic syndromes and acute myeloid leukemia treated with azacitidine.
12. Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?
13. Treatment by Lenalidomide in lower risk myelodysplastic syndrome with 5q deletion—The GFM experience
14. Characteristics and outcome of myelodysplastic syndromes (MDS) with isolated 20q deletion: A report on 62 cases
15. Detection of chromosomal abnormalities associated with chronic lymphocytic leukemia: what is the best method?
16. Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder
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