72 results on '"Forget, Bernard G."'
Search Results
2. Prospects for Gene Therapy of Sickle Cell Disease and Thalassemia
3. NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
4. Animal Models of Hemoglobinopathies and Thalassemia
5. Molecular and Cellular Basis of Hemoglobin Switching
6. Hemoglobins of the Embryo, Fetus, and Adult
7. The Erythrocyte Membrane
8. A Developmental Approach to Hematopoiesis
9. Unusual Types of α Thalassemia
10. Other Sickle Hemoglobinopathies
11. OTHER CLINICALLY IMPORTANT DISORDERS OF HEMOGLOBIN
12. The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin
13. The Pathophysiology and Clinical Features of α Thalassaemia
14. α THALASSEMIA
15. SICKLE CELL DISEASE
16. Genetic Modulation of Sickle Cell Disease and Thalassemia
17. Hemoglobin SC Disease and Hemoglobin C Disorders
18. Stem Cell Transplantation
19. Sickle Cell Trait
20. Nuclear Factors That Regulate Erythropoiesis
21. Population Genetics and Global Health Burden
22. Induction of Fetal Hemoglobin in the Treatment of Sickle Cell Disease and β Thalassemia
23. The Molecular Basis of α Thalassemia
24. Erythropoiesis
25. Introduction, by David J. Weatherall
26. Clinical Aspects of β Thalassemia and Related Disorders
27. Preface
28. PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
29. Unstable Hemoglobins, Hemoglobins with Altered Oxygen Affinity, Hemoglobin M, and Other Variants of Clinical and Biological Interest
30. Plate section
31. Rheology and Vascular Pathobiology in Sickle Cell Disease and Thalassemia
32. Index.
33. Prospects for Gene Therapy of Sickle Cell Disease and Thalassemia.
34. Stem Cell Transplantation.
35. Novel Approaches to Treatment.
36. Induction of Fetal Hemoglobin in the Treatment of Sickle Cell Disease and β Thalassemia.
37. Transfusion and Iron Chelation Therapy in Thalassemia and Sickle Cell Disease.
38. Laboratory Methods for Diagnosis and Evaluation of Hemoglobin Disorders.
39. Genetic Modulation of Sickle Cell Disease and Thalassemia.
40. Population Genetics and Global Health Burden.
41. Dyshemoglobinemias.
42. Unstable Hemoglobins, Hemoglobins with Altered Oxygen Affinity, Hemoglobin M, and Other Variants of Clinical and Biological Interest.
43. Other Sickle Hemoglobinopathies.
44. Hemoglobin SC Disease and Hemoglobin C Disorders.
45. Sickle Cell Pain: Biology, Etiology, and Treatment.
46. Clinical and Pathophysiological Aspects of Sickle Cell Anemia.
47. Hemoglobin E Disorders.
48. Clinical Aspects of β Thalassemia and Related Disorders.
49. The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin.
50. Unusual Types of α Thalassemia.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.