2091 results in Hematology
12 - Animal Models of Hemoglobinopathies and Thalassemia
- from SECTION TWO - PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
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10 - The Biology of Vascular Nitric Oxide
- from SECTION TWO - PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
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Index
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15 - Unusual Types of α Thalassemia
- from SECTION THREE - α THALASSEMIA
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30 - Induction of Fetal Hemoglobin in the Treatment of Sickle Cell Disease and β Thalassemia
- from SECTION EIGHT - NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
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24 - Unstable Hemoglobins, Hemoglobins with Altered Oxygen Affinity, Hemoglobin M, and Other Variants of Clinical and Biological Interest
- from SECTION SIX - OTHER CLINICALLY IMPORTANT DISORDERS OF HEMOGLOBIN
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- 17 August 2009, pp 589-606
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25 - Dyshemoglobinemias
- from SECTION SIX - OTHER CLINICALLY IMPORTANT DISORDERS OF HEMOGLOBIN
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7 - Hemoglobins of the Embryo, Fetus, and Adult
- from SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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19 - Clinical and Pathophysiological Aspects of Sickle Cell Anemia
- from SECTION FIVE - SICKLE CELL DISEASE
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Contents
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27 - Genetic Modulation of Sickle Cell Disease and Thalassemia
- from SECTION SEVEN - SPECIAL TOPICS IN HEMOGLOBINOPATHIES
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26 - Population Genetics and Global Health Burden
- from SECTION SEVEN - SPECIAL TOPICS IN HEMOGLOBINOPATHIES
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Preface
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Frontmatter
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List of Contributors
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17 - Clinical Aspects of β Thalassemia and Related Disorders
- from SECTION FOUR - THE β THALASSEMIAS
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13 - The Molecular Basis of α Thalassemia
- from SECTION THREE - α THALASSEMIA
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SECTION SIX - OTHER CLINICALLY IMPORTANT DISORDERS OF HEMOGLOBIN
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33 - Prospects for Gene Therapy of Sickle Cell Disease and Thalassemia
- from SECTION EIGHT - NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
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SECTION FOUR - THE β THALASSEMIAS
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