656 results on '"Rachmilewitz, Eliezer"'
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2. Toxicity of iron overload and iron overload reduction in the setting of hematopoietic stem cell transplantation for hematologic malignancies
3. The Red Blood Cell In Thalassemia *
4. The Effect of Fermented Papaya Preparation on Radioactive Exposure
5. The frequency of silent cerebral ischemia in patients with transfusion-dependent β-thalassemia major
6. Cerebral infarction in β-thalassemia intermedia: Breaking the silence
7. Iron dosing in kidney disease: inconsistency of evidence and clinical practice
8. Incidence of Anemia and Iron Deficiency in Strenuously Trained Adolescents: Results of a Longitudinal Follow-Up Study
9. Efficient Introduction of Plasmid DNA into Human Hemopoietic Cells by Encapsidation in Simian Virus 40 Pseudovirions
10. Evolution of a Genetic Disease in an Ethnic Isolate: β-Thalassemia in the Jews of Kurdistan
11. Two Mutations in the β-Globin Polyadenylylation Signal Reveal Extended Transcripts and New RNA Polyadenylylation Sites
12. Frequency and distribution of asymptomatic brain lesions in patients with β-thalassemia intermedia
13. Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia
14. Oxidative stress contributes to hemolysis in patients with hereditary spherocytosis and can be ameliorated by fermented papaya preparation
15. Iron overload in MDS—pathophysiology, diagnosis, and complications
16. Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice
17. Lactose intolerance is not the cause of gastrointestinal adverse effects in beta thalassemia patients treated with deferasirox
18. Beta-thalassemia
19. Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2* MRI
20. The antioxidant effect of erythropoietin on thalassemic blood cells
21. Evidence for tissue iron overload in long-term hemodialysis patients and the impact of withdrawing parenteral iron
22. Non-transferrin bound iron in Thalassemia: Differential detection of redox active forms in children and older patients
23. Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes
24. Increased serum hepcidin levels during treatment with deferasirox in iron-overloaded patients with myelodysplastic syndrome
25. Amelioration of Oxidative Stress in Red Blood Cells from Patients with β-thalassemia Major and Intermedia and E-β-thalassemia Following Administration of a Fermented Papaya Preparation
26. Hepcidin and Hfe in iron overload in β-thalassemia
27. The role of antioxidants and iron chelators in the treatment of oxidative stress in thalassemia
28. Decreased hemolysis following administration of antioxidant—fermented papaya preparation (FPP) to a patient with PNH
29. No evidence for myocardial iron overload and free iron species in multitransfused patients with sickle/β0-thalassaemia
30. Future alternative therapies for β-thalassemia
31. Prevalence of iron deficiency and anemia among strenuously trained adolescents
32. Urinary hepcidin excretion in patients with myelodysplastic syndrome and myelofibrosis
33. Cerebrovascular accident in β-thalassemia major (β-TM) and β-thalassemia intermedia (β-TI)
34. Oxidative Imbalance in Hereditary Hemoglobinopathies
35. Frequency of silent cerebral ischemia in patients with transfusion-dependent β-thalassemia major compared to healthy individuals
36. Oxidative stress in red blood cells, platelets and polymorphonuclear leukocytes from patients with myelodysplastic syndrome
37. β-Thalassaemia and sickle cell anaemia as paradigms of hypercoagulability
38. Hemoglobin Switching in Humans Is Accompanied by Changes in the Ratio of the Transcription Factors, GATA-1 and SP1
39. Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera
40. mRNA Expression of Iron Regulatory Genes in β-Thalassemia Intermedia and β-Thalassemia Major Mouse Models
41. Severe infections in thalassaemic patients: prevalence and predisposing factors
42. Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants
43. Medical Progress: (beta)-Thalassemia
44. Exploring the Role of Hepcidin, an Antimicrobial and Iron Regulatory Peptide, in Increased Iron Absorption in β-Thalassemia
45. Role of Iron in Inducing Oxidative Stress in Thalassemia: Can It Be Prevented by Inhibition of Absorption and by Antioxidants?
46. Enhanced aggregability of red blood cells of beta-thalassemia major patients
47. Photosensitization of human bladder carcinoma cells by pyrene-dodecanoic acid: quantitative analysis of the cytotoxicity
48. Decreased hepcidin mRNA expression in thalassemic mice
49. Intrinsic potential for high fetal hemoglobin production in a Druze family with β-thalassemia is due to an unlinked genetic determinant
50. Two mutations in the B-globulin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites
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