1,051 results on '"Vekemans M"'
Search Results
2. COVID-19: impact of vaccination in myeloma patients
3. Diagnostic Yield of Chromosomal Microarray Analysis in Fetuses With Isolated Increased Nuchal Translucency: A French Multicenter Study
4. Gonadotropins and Prolactin
5. Manifestations rares des gammapathies monoclonales : à propos de 2 cas et revue de la littérature
6. P13 IXAZOMIB, DARATUMUMAB AND LOW-DOSE DEXAMETHASONE IN INTERMEDIATE-FIT PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA; RESULTS OF THE INDUCTION AND MAINTENANCE TREATMENT OF THE PHASE II HOVON 143 STUDY
7. Correction: Lenalidomide added to standard intensive treatment for older patients with AML and high-risk MDS
8. Comparative value of post-remission treatment in cytogenetically normal AML subclassified by NPM1 and FLT3-ITD allelic ratio
9. Gastrointestinal Nuclear Medicine
10. Comparative therapeutic value of post-remission approaches in patients with acute myeloid leukemia aged 40–60 years
11. Three-dimensional reconstruction of the lower limb’s venous system in human fetuses using the computer-assisted anatomical dissection (CAAD) technique
12. Diffuse vertebral marrow changes at MRI: Multiple myeloma or normal?
13. COVID-19: impact of vaccination in myeloma patients.
14. P906: IXAZOMIB, DARATUMUMAB AND LOW DOSE DEXAMETHASONE IN FRAIL PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA (NDMM): RESULTS OF THE MAINTENANCE TREATMENT OF THE PHASE II HOVON 143 STUDY
15. P12: TREATMENTS IN PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA: RETROSPECTIVE CHART REVIEW OF REAL-WORLD OUTCOMES FOR STANDARD OF CARE
16. Resistance prediction in AML: analysis of 4601 patients from MRC/NCRI, HOVON/SAKK, SWOG and MD Anderson Cancer Center
17. Differential association of calreticulin type 1 and type 2 mutations with myelofibrosis and essential thrombocytemia: relevance for disease evolution
18. Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy
19. Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma
20. A general chemotherapy myelotoxicity score to predict febrile neutropenia in hematological malignancies
21. Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases
22. Diffuse vertebral marrow changes at MRI: Multiple myeloma or normal?
23. Inferior outcome of addition of the aminopeptidase inhibitor tosedostat to standard intensive treatment for elderly patients with aml and high risk mds
24. Causes of fever in cancer patients (prospective study over 477 episodes)
25. NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique
26. Low mannose-binding lectin concentration is associated with severe infection in patients with hematological cancer who are undergoing chemotherapy
27. La CGH array : un bouleversement de la pratique hospitalière en cytogénétique
28. Febrile neutropenia and Fusobacterium bacteremia: clinical experience with 13 cases
29. OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment
30. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH
31. Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10p
32. Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain
33. Bortezomib (Velcade)-thalidomide-dexamethasone is superior to thalidomide-dexamethasone in patients with multiple myeloma progressing or relapsing after autologous transplantation: 0117
34. LRRFIP1, a new FGFR1 partner gene associated with 8p11 myeloproliferative syndrome
35. Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocation
36. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies
37. 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation
38. Rare IgH/14q32 Translocations in Multiple Myeloma: B390
39. Multiple Myeloma in Black Africans: Does It Behave Differently?: A626
40. Osteonecrosis of the Jaw in Multiple Myeloma Patients: Risk Factors of Early ONJ, Decreased Impact After 2005: A120
41. The t(14;20)(q32;q12): A Rare Cytogenetic Change in Multiple Myeloma (MM) Associated with Poor Outcome: A182
42. Diagnostic préimplantatoire
43. Diagnostic génétique préimplantatoire et grossesses spontanées : un passage à l'acte inattendu
44. La CGH microarray : principe et applications en pathologie constitutionnelle
45. L’expérience parisienne du diagnostic génétique pré-implantatoire (DPI) : bilan des premières naissances
46. Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia
47. Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene
48. EUROPEAN PATIENT SAFETY POST-AUTHORIZATION STUDY WITH MULTIPLE REFRACTORY MYELOMA OR IN RELAPSE TREATED WITH POMALIDOMIDE IN HABITUAL PRACTICE
49. Genotype–phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions
50. Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: A Case Report
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