688 results on '"Michaux, L."'
Search Results
2. Development of CuAlNi Shape Memory Alloy Structures Using Cold Spray Deposition Technique with Laser Remelting
3. Nouveautés dans la prise en charge des pneumopathies d’hypersensibilité
4. Hot methane line lists for exoplanet and brown dwarf atmospheres
5. RPL5 on 1p22.1 is recurrently deleted in multiple myeloma and its expression is linked to bortezomib response
6. Correction: Lenalidomide added to standard intensive treatment for older patients with AML and high-risk MDS
7. The CADM1 tumor suppressor gene is a major candidate gene in MDS with deletion of the long arm of chromosome 11
8. 60 Comprehensive genome-wide analysis of non-invasive test data allows accurate cancer prediction: a retrospective analysis of over 85.000 pregnancies
9. miR-15a-5p and miR-21-5p contribute to chemoresistance in cytogenetically normal acute myeloid leukaemia by targeting PDCD4, ARL2 and BTG2
10. Translocation t(14;18) is not associated with inferior outcome in chronic lymphocytic leukemia
11. FIP1L1-PDGFRα D842V, a novel panresistant mutant, emerging after treatment of FIP1L1-PDGFRα T674I eosinophilic leukemia with single agent sorafenib
12. Heterogeneous patterns of amplification of the NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia
13. An Unusual Course of Donor-Transmitted Angiosarcoma after Lung Transplantation
14. Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL
15. Chromosomal translocations independently predict treatment failure, treatment-free survival and overall survival in B-cell chronic lymphocytic leukemia patients treated with cladribine
16. A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation
17. Addition of lenalidomide to intensive treatment in younger and middle-aged adults with newly diagnosed AML: the HOVON-SAKK-132 trial
18. Het ondernemingsbegrip in het mededingingsrecht, het marktpraktijkenrecht en het consumentenrecht
19. A rare cause of high liver stiffness
20. Cytogenetics and molecular genetics of T-cell acute lymphoblastic leukemia: from thymocyte to lymphoblast
21. A rare cause of high liver stiffness
22. miR-15a-5p and miR-21-5p contribute to chemoresistance in cytogenetically normal acute myeloid leukaemia by targeting PDCD4, ARL2 and BTG2
23. Het ondernemingsbegrip in het mededingingsrecht, het marktpraktijkenrecht en het consumentenrecht
24. Correction: Lenalidomide added to standard intensive treatment for older patients with AML and high-risk MDS
25. Fluorescence in situ hybridization analysis of 110 hematopoietic disorders with chromosome 5 abnormalities: do de novo and therapy-related myelodysplastic syndrome–acute myeloid leukemia actually differ?
26. FOXP1, a gene highly expressed in a subset of diffuse large B-cell lymphoma, is recurrently targeted by genomic aberrations
27. Translocation t(1;6)(p35.3;p25.2): a new recurrent aberration in ‘unmutated’ B-CLL
28. ‘Wait a Minute, Mr Postman’: On Universal Service, the Postal Services Directive and the SGEI Framework · Joined Cases C-431/19 P and C-432/19 P Inpost · Annotation by Joris Gruyters and Lennard Michaux
29. Coexistence of BCL1/CCND1 and CMYC aberrations in blastoid mantle cell lymphoma: a rare finding associated with very poor outcome
30. Translocation t(2;3)(p15–23;q26–27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features
31. High incidence of complications after 2-chloro-2’-deoxyadenosine combined with cyclophosphamide in patients with advanced lymphoproliferative malignancies
32. Clinical and molecular features of FIP1L1-PDFGRA (+) chronic eosinophilic leukemias
33. t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH)
34. Genetics of Chronic Lymphocytic Leukemia: Practical Aspects and Prognostic Significance
35. Concurrent spinal cord and vertebral bone marrow radionecrosis 8 years after therapeutic irradiation
36. Atypical lymphocytic leukemia and mantle cell lymphoma immunologically very close: flow cytometric distinction by the use of CD20 and CD54 expression
37. Complex karyotype and absence of mutation in the c-kit receptor in aggressive mastocytosis presenting with pelvic osteolysis, eosinophilia and brain damage
38. IL-TIF/IL-22: genomic organization and mapping of the human and mouse genes
39. Phase I/II study of 2-chloro-2′-deoxyadenosine with cyclophosphamide in patients with pretreated B cell chronic lymphocytic leukemia and indolent non-Hodgkin's lymphoma
40. The value of interphase fluorescence in situ hybridization for the detection of translocation t(12;21) in childhood acute lymphoblastic leukemia
41. Life Cycle Costing
42. Corona and EU Economic Law
43. MafB oncoprotein detected by immunohistochemistry as a highly sensitive and specific marker for the prognostic unfavorable t(14;20) (q32;q12) in multiple myeloma patients
44. Magnetic resonance imaging of the bone marrow in hematological malignancies
45. Trisomy 3q11-q29 is recurrently observed in B-cell non-Hodgkin's lymphomas associated with cold agglutinin syndrome
46. Rare IgH/14q32 Translocations in Multiple Myeloma: B390
47. Multiple Myeloma in Black Africans: Does It Behave Differently?: A626
48. The t(14;20)(q32;q12): A Rare Cytogenetic Change in Multiple Myeloma (MM) Associated with Poor Outcome: A182
49. Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization
50. Sustained, clonal karyotype abnormalities in the Philadelphia chromosome negative cells of CML patients successfully treated with Imatinib
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