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Contributors | |
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Preface | |
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Clinical Evaluation of the Patient | |
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Initial Approach to the Patient: History and Physical Examination | |
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Examination of Blood Cells | |
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Examination of the Marrow, Daniel H. Ryan | |
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the Organization of the Lymphohematopoietic Tissues | |
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Structure of the Marrow and the Hematopoietic Microenvironment | |
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The Organization and Structure of Lymphoid Tissues | |
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Epochal Hematology | |
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Hematology of the Fetus and Newborn | |
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Hematology during Pregnancy | |
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Hematology in Older Persons | |
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Molecular and Cellular Hematology | |
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Genetic Principles and Molecular Biology | |
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Genomics and Epigenetics | |
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Cytogenetics and Molecular Abnormalities | |
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Apoptosis | |
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Cell-Cycle Regulation and Hematologic Disorders | |
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Signal Transduction Pathways | |
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The Cluster of Differentiation Antigens | |
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Hematopoietic Stem Cells | |
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The Inflammatory Process | |
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Innate Immunity | |
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Dendritic Cells and the Control of Innate Adaptive Immunity | |
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Therapeutic Principles | |
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Pharmacology and Toxicity of Antineoplastic Drugs | |
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Principles of Hematopoietic Cell Transplantation | |
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Treatment of Infections in the Immunocompromised Host | |
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Principles of Antithrombotic Therapy | |
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Principles of Immune Cell Therapy | |
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Principles of Vaccine Therapy | |
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Principles of Therapeutic Apheresis: Indications, Efficacy, and Complications | |
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Principles of Gene Transfer for Therapy | |
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Regenerative Medicine: Principles of Multipotential Cell Therapy for Tissue Replacement | |
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The Erythrocyte | |
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Morphology of the Erythron | |
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Composition of the Erythrocyte, Ernest Beutler | |
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Production of Erythrocytes | |
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Destruction of Erythrocytes, Ernest Beutler | |
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Clinical Manifestations and Classification of Erythrocyte Disorders | |
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Aplastic Anemia: Acquired and Inherited | |
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Pure Red Cell Aplasia | |
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Anemia of Chronic Renal Disease | |
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Anemia of Chronic Disease | |
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Anemia of Endocrine Disorders | |
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The Congenital Dyserythropoietic Anemias | |
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Paroxysmal Nocturnal Hemoglobinuria | |
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Folate, Cobalamin, and Megaloblastic Anemias | |
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Disorders of Iron Metabolism, Ernest Beutler | |
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Anemia Resulting from Other Nutritional Deficiencies | |
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Anemia Associated with Marrow Infiltration | |
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The Red Blood Cell Membrane and Its Disorders: Hereditary Spherocytosis, Elliptocytosis, and Related Diseaes | |
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Disorders of Red Cells Resulting from Enzyme Abnormalities | |
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The Thalassemias: Disorders of Globin Synthesis | |
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Disorders of Hemoglobin Structure: Sickle Cell Anemia and Related Abnormalities | |
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Methemoglobinemia and Other Dyshemoglobinemias | |
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Hemolytic Anemia Resulting from Physical Injury to Red Cells | |
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Hemolytic Anemia Resulting from Chemical and Physical Agents | |
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Hemolytic Anemia Resulting from Infections with Microorganisms | |
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Hemolytic Anemia Resulting from Immune Injury | |
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Alloimmune Hemolytic Disease of the Fetus and Newborn | |
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Hypersplenism and Hyposlenism | |
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Primary and Secondary Polycythemias (Erythrocytosis) | |
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The Porphyrias | |
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Hereditary and Acquired Sideroblastic Anemias | |
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Neutrophils, Eosinophils, Basophils, and Mast Cells | |
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Morphology of Neutrophils, Eosinophils, and Basophils | |
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Composition of Neutrophils | |
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Production, Distribution, and Fate of Neutrophils | |
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Eosinophils and Their Disorders | |
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Basophils and Mast Cells and Their Disorders | |
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Classification and Clinical Manifestations of Neutrophil Disorders | |
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Neutropenia and Neutrophilia | |
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Disorders of Neutrophil Function | |
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Monocytes and Macrophages | |
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Morphology of Monocytes and Macrophages | |
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Biochemistry and Functions of Monocytes and Macrophages | |
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Production, Distribution, and Fate of Monocytes and Macrophages | |
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Classification and Clinical Manifestations of Disorders of Monocytes and Macrophages | |
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Monocytosis and Monocytopenia | |
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Inflammatory and Malignant Histiocytosis | |
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Lipid Storage Diseases | |
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Lymphocytes and Plasma Cells | |
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Morphology of Lymphocytes and Plasma Cells | |
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Composition and Biochemistry of Lymphocytes and Plasma Cells | |
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Lymphopoiesis | |
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Functions of B Lymphocytes and Plasma Cells in Immunoglobulin Production | |
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Functions of T Lymphocytes: T-Cell Receptors for Antigen | |
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Functions of Natural Killer Cells | |
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Classification and Clinical Manifestations of Lymphocyte and Plasma Cell Disorders | |
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Lymphocytosis and Lymphocytopenia | |
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Immunodeficiency Diseases | |
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Hematologic Manifestations of Acquired Immunodeficiency Syndrome | |
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Mononucleosis Syndromes | |
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Neoplastic Myeloid Diseases | |
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Classification and Clinical Manifestations of the Clonal Myeloid Disorders | |
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Polycythemia Vera | |
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Essential Thrombocythemia | |
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Myelodysplastic Syndromes (Clonal Cytopenias and Oligoblastic Myelogenous Leukemia) | |
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Acute Myelogenous Leukemia | |
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Chronic Myelogenous Leukemia and Related Disorders | |
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Primary Myelofibrosis | |
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Neoplastic Lymphoid Diseases | |
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Classification of Malignant Lymphoid Disorders | |
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Acute Lymphoblastic Leukemia | |
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Chronic Lymphocytic Leukemia and Related Diseases | |
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Hairy Cell Leukemia | |
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Large Granular Lymphocytic Leukemia | |
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General Considerations of Lymphoma: Epidemiology, Etiology, Heterogeneity, and Primary Extranodel Disease | |
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Pathology of Malignant Lymphomas | |
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Hodgkin Lymphoma | |
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Diffuse Large B-Cell Lymphoma | |
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Follicular Lymphoma | |
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Mantle Cell Lymphoma | |
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Marginal Zone B-Cell Lymphomas | |
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Burkitt Lymphoma | |
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Cutaneous T-Cell Lymphoma (Mycosis Fungoides and Sezary Syndrome) | |
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Mature T-Cell and Natural Killer Cell Lymphomas | |
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Plasma Cell Neoplasms: General Considerations, H. Elizabeth Broome | |
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Essential Monoclonal Gammopathy | |
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Myeloma | |
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The Amyloidoses | |
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Macroglobulinemia | |
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Heavy-Chain Disease | |
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Hemostatis and Thrombosis | |
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Megakaryopoiesis and Thrombopoiesis | |
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Platelet Morphology, Biochemistry, and Function | |
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Molecular Biology and Biochemistry of the Coagulation Factors and Pathways of Hemostatis | |
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Control of Coagulation Reactions | |
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Vascular Function in Hemostatis | |
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Classification, Clinical Manifestations, and Evaluation of Disorders of Hemostatis | |
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Thrombocytopenia | |
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Reactive Thrombocytosis | |
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Hereditary Qualitative Platelet Disorders | |
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Acquired Qualitative Platelet Disorders | |
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The Vascular Purpuras | |
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Hemophilia a and Hemophilia B | |
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Inherited Deficiencies of Coagulation Factors II, V, VII, X, XI, and XIII and Combined Deficiencies of Factors V and VIII and of the Vitamin K-Dependent Factors | |
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Hereditary Fibrinogen Abnormalities | |
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Von Willebrand Disease | |
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Antibody-Mediated Coagulation Factor Deficiencies, Pete Lollar | |
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Hemostatic Dysfunction Related to Liver Diseases and Liver Transplantation | |
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Disseminated Intravascular Coagulation | |
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Hereditary Thrombophilia | |
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The Antiphospholipid Syndrome | |
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Antibody-Mediated Thrombotic Disorders: Thrombotic-Thrombocytopenic Purpura and Heparin-Induced Thrombocytopenia | |
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Venous Thrombosis | |
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Atherothrombosis: Disease Initiation, Progression, and Treatment | |
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Fibrinolysis and Thrombolysis | |
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Transfusion Medicine | |
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Erythrocyte Antigens and Antibodies | |
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Human Leukocyte and Platelet Antigens | |
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Blood Procurement and Screening | |
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Red Cell Transfusion | |
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Preservation and Clinical Use of Platelets | |
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Index | |