159 results on '"Menif, Samia"'
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2. A regionally based precision medicine implementation initiative in North Africa:The PerMediNA consortium
3. New Born Screening of Hemoglobinopathies in a Center Tunisian Population
4. Emotional and behavioral attitudes of Tunisian youth towards childhood leukemia: health education and primary prevention in perspective
5. Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia
6. EZH2, new diagnosis and prognosis marker in acute myeloid leukemia patients
7. Coinheritance of HbO Arab/β 0 -thalassemia with Severe Manifestation in Newborn.
8. Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging.
9. TP53 Gene 72 Arg/Pro (rs1042522) single nucleotide polymorphism increases the risk and the severity of chronic lymphocytic leukemia
10. PB2543: CIRCULATING MICROVESICLES AS POTENTIAL CELLULAR BIOMARKERS FOR THROMBOTIC RISKS IN BETA THALASSEMIA
11. PB2526: UMBILICAL CORD BLOOD SCREENING FOR SICKLE CELL DISEASE: A PILOT STUDY IN THE NORTH OF TUNISIA
12. PB1717: CD19-NEGATIVE B- ACUTE LYMPHOBLASTIC LEUKEMIA: WHAT CHALLENGES?
13. PB1722: EARLY T-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA: DIAGNOSIS AND TREATMENT CHALLENGES
14. A regionally based precision medicine implementation initiative in North Africa:The PerMediNA consortium
15. In Ph+BCR-ABL1P210+ acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent
16. Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study
17. Chronic myeloid leukemia patients in Tunisia: epidemiology and outcome in the imatinib era (a multicentric experience)
18. CHRONIC MYELOID LEUKEMIA IN CHILDREN AND YOUNG ADULTS IN TUNISIA
19. Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach.
20. Molecular study of ABCB1 gene and its correlation with imatinib response in chronic myeloid leukemia
21. Regulatory network analysis of microRNAs and genes in imatinib-resistant chronic myeloid leukemia
22. hOCT1 gene expression predict for optimal response to Imatinib in Tunisian patients with chronic myeloid leukemia
23. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family
24. Epidemiology of Chronic Myeloid Leukemia in Tunisia
25. Tyrosol Derivatives, Bearing 3,5-Disubstituted Isoxazole and 1,4-Disubstituted Triazole, as Potential Antileukemia Agents by Promoting Apoptosis
26. Hematological relevance of JAK2 V617F and calreticulin mutations in Tunisian patients with essential thrombocythemia
27. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ) 0 -Thalassemia among Tunisian family.
28. KIT mutation detection in Tunisian patients with newly diagnosed myelogenous leukemia: prevalence and prognostic significance
29. Coinheritance of HbO Arab/β0-thalassemia with Severe Manifestation in Newborn
30. JAK2 p.(V617F) mutation in Tunisian myeloproliferative neoplasms and its genotype-phenotype correlation
31. Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.
32. The prevalence and prognostic significance of KRAS mutation in bladder cancer, chronic myeloid leukemia and colorectal cancer
33. Genetic polymorphisms of NQO1, CYP1A1 and TPMT and susceptibility to acute lymphoblastic leukemia in a Tunisian population
34. ATRA and anthracycline-based chemotherapy in the treatment of childhood acute promyelocytic leukemia (APL): A 10-year experience in Tunisia
35. First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby
36. Additional file 2 of Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study
37. Additional file 1 of Identification of genes and miRNA associated with idiopathic recurrent pregnancy loss: an exploratory data mining study
38. Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions
39. Recurrent differentiation syndrome or septic shock? Unresolved dilemma in a patient with acute promyelocytic leukemia
40. Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency.
41. The proportion of different BCR-ABL1 transcript types in chronic myeloid leukemia. An international overview
42. JAK2 p.(V617F) mutation in Tunisian myeloproliferative neoplasms and its genotypephenotype correlation.
43. In Ph+BCR-ABL1P210+ acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent
44. Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians.
45. Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance
46. Regulatory network analysis of microRNAs and genes in imatinib-resistant chronic myeloid leukemia
47. Association of genetic variation inIKZF1, ARID5B, CDKN2A, andCEBPEwith the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence
48. Polymorphisms in XPC, XPD and XPG DNA repair genes and leukemia risk in a Tunisian population
49. Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance.
50. In Ph+BCR-ABL1P210+acute lymphoblastic leukemia the e13a2 (B2A2) transcript is prevalent
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