2091 results in Hematology
SECTION FIVE - SICKLE CELL DISEASE
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2 - Erythropoiesis
- from SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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1 - A Developmental Approach to Hematopoiesis
- from SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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28 - Laboratory Methods for Diagnosis and Evaluation of Hemoglobin Disorders
- from SECTION SEVEN - SPECIAL TOPICS IN HEMOGLOBINOPATHIES
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- 17 August 2009, pp 658-686
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SECTION TWO - PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
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20 - Sickle Cell Pain: Biology, Etiology, and Treatment
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Plate section
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32 - Stem Cell Transplantation
- from SECTION EIGHT - NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
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Disorders of Hemoglobin
- Genetics, Pathophysiology, and Clinical Management
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31 - Novel Approaches to Treatment
- from SECTION EIGHT - NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
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- 17 August 2009, pp 755-773
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9 - The Erythrocyte Membrane
- from SECTION TWO - PATHOPHYSIOLOGY OF HEMOGLOBIN AND ITS DISORDERS
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5 - Molecular and Cellular Basis of Hemoglobin Switching
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23 - Other Sickle Hemoglobinopathies
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- 17 August 2009, pp 564-586
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18 - Hemoglobin E Disorders
- from SECTION FOUR - THE β THALASSEMIAS
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6 - Structure and Function of Hemoglobin and Its Dysfunction in Sickle Cell Disease
- from SECTION ONE - THE MOLECULAR, CELLULAR, AND GENETIC BASIS OF HEMOGLOBIN DISORDERS
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14 - The Pathophysiology and Clinical Features of α Thalassaemia
- from SECTION THREE - α THALASSEMIA
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Foreword, by H. Franklin Bunn
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SECTION EIGHT - NEW APPROACHES TO THE TREATMENT OF HEMOGLOBINOPATHIES AND THALASSEMIA
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- 17 August 2009, pp 687-688
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SECTION SEVEN - SPECIAL TOPICS IN HEMOGLOBINOPATHIES
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- 17 August 2009, pp 623-624
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