2091 results in Hematology
Chapter 13c - Management of obstetric hemorrhage: hemostatic management
- from Section 5 - Hemorrhagic disorders
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Section 4 - Thrombophilia and fetal loss
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Section 3 - Thromboembolism and anticoagulation
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Section 5 - Hemorrhagic disorders
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Chapter 16 - Genetic counseling and pre-natal diagnosis in hemophilia
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Chapter 9 - Prosthetic heart valves
- from Section 3 - Thromboembolism and anticoagulation
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Chapter 15 - Inherited coagulopathies
- from Section 5 - Hemorrhagic disorders
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Section 7 - Malignant conditions
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Chapter 2 - Hematinic deficiencies
- from Section 1 - Cellular changes
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Contributors
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4 - Nuclear Factors That Regulate Erythropoiesis
- from SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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- Disorders of Hemoglobin
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- 17 August 2009, pp 62-85
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29 - Transfusion and Iron Chelation Therapy in Thalassemia and Sickle Cell Disease
- from SECTION EIGHT - NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
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- 17 August 2009, pp 689-744
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21 - Hemoglobin SC Disease and Hemoglobin C Disorders
- from SECTION FIVE - SICKLE CELL DISEASE
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- 17 August 2009, pp 525-548
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11 - Mechanisms and Clinical Complications of Hemolysis in Sickle Cell Disease and Thalassemia
- from SECTION TWO - PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
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- 17 August 2009, pp 201-224
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8 - Rheology and Vascular Pathobiology in Sickle Cell Disease and Thalassemia
- from SECTION TWO - PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
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- 17 August 2009, pp 139-157
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SECTION THREE - α THALASSEMIA
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3 - The Normal Structure and Regulation of Human Globin Gene Clusters
- from SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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22 - Sickle Cell Trait
- from SECTION FIVE - SICKLE CELL DISEASE
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- 17 August 2009, pp 549-563
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16 - The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin
- from SECTION FOUR - THE β THALASSEMIAS
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- 17 August 2009, pp 323-356
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Introduction, by David J. Weatherall
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- 17 August 2009, pp xix-xx
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