132 results on '"Shaheen, Iman A."'
Search Results
2. Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian β-Thalassemia Major Patients
3. Vitamin D receptor polymorphisms and vitamin D insufficiency are not associated with sepsis in critically ill children: a case-control study
4. Thrombin activatable fibrinolysis inhibitor plasma levels and TAFI Thr325Ile genetic polymorphism in a cohort of Egyptian sickle cell disease patients and impact on disease severity.
5. Thrombin Activatable Fibrinolysis Inhibitor (TAFI) Plasma Levels and Thr325Ile Genetic Polymorphism in a Cohort of Egyptian Sickle Cell Disease Patients and Impact on Disease Severity
6. Usefulness of serum osteopontin level as a noninvasive parameter of portal hypertension
7. Vitamin D Insufficiency is Not Associated With Pediatric and Adolescent Immune Thrombocytopenia: A Study in Conjunction With its Receptor Genetic Polymorphisms
8. Platelets count and platelets indices; mean platelet volume and plateletcrit in pediatric chronic lung disease
9. L-Selectin P213S and Integrin Alpha 2 C807T Genetic Polymorphisms in Pediatric Sickle Cell Disease Patients
10. Polymorphisms of xeroderma pigmentosum genes (XPC, XPD, and XPG) and susceptibility to acute leukemia among a sample of Egyptian patients
11. Hematological Findings in Nephropathic Cystinosis: Single Center Experience.
12. Genetic Variations of ferroportin-1(FPN1-8CG), TMPRSS6 (rs855791) and Hemojuvelin (I222N and G320V) Among a Cohort of Egyptian β-Thalassemia Major Patients
13. Association of μ-opioid receptor gene polymorphism (A118G) with variations in fentanyl analgesia consumption after total abdominal hysterectomy in female Egyptian patients
14. The association between hepatitis C virus infection, genetic polymorphisms of oxidative stress genes and B-cell non-Hodgkin’s lymphoma risk in Egypt
15. IMPACT OF SUPEROXIDE DISMUTASE GENETIC POLYMORPHISM (SOD2 VAL16ALA) AND SUPEROXIDE DISMUTASE LEVEL ON DISEASE SEVERITY IN A COHORT OF EGYPTIAN SICKLE CELL DISEASE PATIENTS IN EGYPT
16. Association between matrix metalloproteinase 2 (MMP2) promoter polymorphisms and the susceptibility to non-Hodgkin’s lymphoma in Egyptians
17. Methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in chronic myeloid leukemia: an Egyptian study
18. Prevalence of factor V Leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease
19. Clinical relevance of angiopoietin-1, angiopoietin-2, and their receptor Tie-2 expression in acute myeloid leukemia
20. Flow cytometric detection of leukemic stem cells (LSCs) in Egyptian pediatric B-acute lymphoblastic leukemia
21. The osteogenic differentiation potentials of umbilical cord blood hematopoietic stem cells
22. The clinical significance of methylenetetrahydrofolate reductase (MTHFR) polymorphisms in acute lymphoblastic leukemia
23. Clinical relevance of angiopoietin-1, angiopoietin-2, and their receptor Tie-2 expression in acute myeloid leukemia
24. A Localized Case–Control Study of Extra-Gastric Manifestations of Helicobacter pylori Infection in Children
25. Klotho Level as a Marker of Low Bone Mineral Density in Egyptian Sickle Cell Disease Patients
26. Detection of Renal Insufficiency in a Cohort of Patients With Beta-thalassemia Major Using Cystatin-C
27. Quantitative Assessment of Wilms Tumor 1 (WT1) Gene Transcripts in Egyptian Acute Lymphoblastic Leukemia Patients
28. Detection of miR-1246, miR-23a and miR-451 in sera of colorectal carcinoma patients: a case-control study in Cairo University hospital
29. Elevated serum KL-6 in pediatric asthma exacerbation: a proof of alveolar injury
30. The Relation Between Maternal / Neonatal Vitamin D Levels and Early Onset Neonatal Sepsis
31. Klotho Level as a Marker of Low Bone Mineral Density in Egyptian Sickle Cell Disease Patients.
32. The prevalence of combined vascular endothelial growth factor, endothelial nitric oxide synthase and thrombin‐activatable fibrinolysis inhibitor genetic polymorphisms among Egyptian patients with recurrent spontaneous abortion
33. Breast cancer resistance protein (BCRP) gene expression in a cohort of adult Egyptian patients with acute myeloid leukemia
34. Erratum to: A Localized Case–Control Study of Extra-Gastric Manifestations of Helicobacter pylori Infection in Children
35. Thrombin-Activatable Fibrinolysis Inhibitor Gene Polymorphism (TAFI1040C/T) in Women With Recurrent Spontaneous Abortion
36. Thrombin-Activatable Fibrinolysis Inhibitor Gene Polymorphism (TAFI1040C/T) in Women With Recurrent Spontaneous Abortion.
37. Peripheral expression of hepcidin gene in Egyptian β-thalassemia major
38. Glutathione S-Transferase Gene Polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian Pediatric Patients with Sickle Cell Disease
39. Association of μ-opioid receptor gene polymorphism (A118G) with variations in fentanyl analgesia consumption after total abdominal hysterectomy in female Egyptian patients
40. Apolipoprotein E Gene Polymorphism And The Risk Of Left Ventricular Dysfunction Among Egyptian Β-thalassemia Major.
41. Detection of Trisomy 4 and 10 in Egyptian Pediatric Patients with Acute Lymphoblastic Leukemia
42. Methylene tetrahydrofolate reductase (MTHFR) gene polymorphisms in chronic myeloid leukemia: an Egyptian study
43. Apolipoprotein E gene polymorphism and the risk of left ventricular dysfunction among Egyptian β-thalassemia major
44. Detection of expression of IL-18 and its binding protein in Egyptian pediatric immune thrombocytopenic purpura
45. Detection of expression of IL-18 and its binding protein in Egyptian pediatric immune thrombocytopenic purpura
46. DNMT3B promoter polymorphism and risk of immune thrombocytopenic purpura in pediatric Egyptians
47. Prevalence of factor V Leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease
48. Detection of Orphan Receptor Tyrosine Kinase (ROR-1) Expression in Egyptian Pediatric Acute Lymphoblastic Leukemia
49. FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt
50. Incidence and Association of 563 C/T Mediterranean and the Silent 1311C/T G6PD Mutations in G6PD-deficient Egyptian Children
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