ウィリアムズ血液学(第6版)<br>Williams Hematology (6TH)

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ウィリアムズ血液学(第6版)
Williams Hematology (6TH)

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  • 製本 Hardcover:ハードカバー版/ページ数 1941 p.
  • 言語 ENG
  • 商品コード 9780070703971
  • DDC分類 616.15

基本説明

This popular classic reference is thoroughly updated with expanded coverage of treatment and management new material on the clinical aspects and classification of such conditions as myeloid malignancies and malignant lymphoid disorders.

Full Description

This popular classic reference in hematologic disorders is thoroughly updated with expanded coverage of treatment and management.

Contents

Part I: Clinical Evaluation of the Patient 1: Approach to the Patient. 2: Examination of the Blood. 3: Examination of the Marrow. Part II: General Hematology. 4: Structure of the Marrow. 5: Spleen and Other Lymphoid Tissues. 6: The Inflammatory Response. 7: Hematology of The Newborn. 8: Hematology in The Aged. Part III: Molecular and Cellular Hematology. 9: Genetic Principles and Molecular Biology. 10: Cytogenetics and Gene Rearrangement. 11: Apoptosis. 12: Principles of Cell Regulation. 13: The Cluster of Differentiation (CD) Antigens. 14: Hematopoietic Stem Cells, Progenitor Cells, and Cytokines. 15: Immune Accessory Molecules and Signal Transduction. Part IV: Therapeutic Principles. 16: Pharmacology and Toxicity of Antineoplastic Drugs. 17: Treatment of Infections in The Immunocompromised Host. 18: Allogeneic and Autologous Stem Cell Transplantation. 19: Gene Therapy. 20: The Use of Venous Access Devices. 21: Pain Management. Part V: The Erythrocyte. 22: Morphology of The Erythron. 23: Composition of The Erythrocyte. 24: Iron Metabolism. 25: Metabolic Aspects of Folic Acid and Cobalamin. 26: Energy Metabolism and Maintenance of Erythrocytes. 27: The Red Cell Membrane 28: Structure and Function of Hemoglobin. 29: Production and Destruction of Erythrocytes. 30: Clinical Manifestations and Classification of Erythrocyte Disorders. 31: Aplastic Anemia. 32: Pure Red Cell Aplasia. 33: Anemia of Chronic Renal Failure. 34: Anemia of Endocrine Disorders. 35: The Congenital Dyserythropoietic Anemias. 36: Paroxysmal Nocturnal Hemoglobinuria. 37: The Megaloblastic Anemias. 38: Iron Deficiency. 39: Anemia Due to Other Nutritional Deficiencies. 40: Anemia Associated With Marrow Infiltration. 41: Anemia of Chronic Disease. 42: Disorders of Iron Transport and Storage. 43: Hereditary Spherocytosis, Elliptocytosis and Related Disorders. 44: Acanthocytosis, Stomatocytosis, and Related Disorders. 45: G 6 Phosphate Dehydrogenase Deficiency and Other Red Cell Enzyme Abnormalities. 46: The Thalassemias. 47: The Sickle Cell Diseases and Related Disorders. 48: Hemoglobinopathies Associated With Unstable Hemoglobin. 49: Methemoglobinemia and Other Causes of Cyanosis. 50: Traumatic Cardiac Hemolytic Anemia. 51: Microangiopathic Hemolytic Anemia. 52: March Hemoglobinuria, Sports Anemia, and Space Anemia. 53: Hemolytic Anemia Due to Chemical and Physical Agents. 54: Hemolytic Anemia Due to Infections With Microorganisms. 55: Acquired Hemolytic Anemia Due to Warm- Reacting Autoantibodies. 56: Cryopathic Hemolytic Syndromes 57: Drug- Related Immune Hemolytic Anemia. 58: Alloimmune Hemolytic Disease of the Newborn. 59: Acute Blood Loss Anemia. 60: Hypersplenism and Hyposplenism. 61: Polycythemia. 62: The Hematologic Aspects of Porphyria. 63: Hereditary and Acquired Sideroblastic Anemias. Part VI: Neutrophils, Eosinophils, Basophils and Mast Cells. 64: Morphology of Neutrophils, Eosinophils, and Basophils. 65: Composition of Neutrophils. The Metabolism of Neutrophils 66: Production, Distribution, and Fate of Neutrophils. 67: Functions of Neutrophils. 68: Eosinophils and Their Disorders. 69: Production, Biochemistry, and Function of Basophils and Mast Cells. Basophilopenia, Basophilia, and Mastocytosis. 70: Classification and Clinical Manifestations of Neutrophil Disorders. 71: Neutropenia. and Neutrophilia. 72: Neutrophil Disorders: Qualitative Abnormalities of the Neutrophil. Part VII: Monocytes and Macrophages. 73: Morphology of Monocytes and Macrophages. 74: Biochemistry and Function of Monocytes and Macrophages. 75: Production, Distribution, and Fate of Monocytes and Macrophages. 76: Classification and Clinical Manifestations of Disorders of Monocytes and Macrophages. 77: Monocytosis and Monocytopenia. 78: Inflammatory and Malignant Histiocytosis. 79: Lipid Storage Diseases. Part VIII: Lymphocytes and Plasma Cells. 80: Morphology of Lymphocytes and Plasma Cells. 81: Composition and Biochemistry of Lymphocytes and Plasma Cells. 82: Lymphoid Ontogeny and Homing Receptors. 83: Functions of B Lymphocytes and Plasma Cells in Immunoglobulin. 84: Functions of T Lymphocytes: T-Cell Receptors for Antigen. 85: Functions of Natural Killer Cells. 86: Classification and Clinical Manifestation of Lymphocyte and... 87: Lymphocytosis and Lymphocytopenia. 88: Immunodeficiency Diseases. 89: Acquired Immunodeficiency Syndrome (AIDS). 90: Mononucleosis Syndromes. Part IX: Malignant Diseases. 91: Classification of Myeloid Malignancies. 92: Myelodysplastic Disorders. 93: Acute Myelogenous Leukemia. 94: Chronic Myelogenous Leukemia and Related Disorders. 95: Idiopathic Myelofibrosis (Agnogenic Myeloid Metaplasia). 96: Classification of Malignant Lymphoid Disorders. 97: Acute Lymphocytic Leukemia. 98: Chronic Lymphocytic Leukemia and Related Diseases. 99: Hairy Cell Leukemia. 100: Large Granular Lymphocytic Leukemia. 101: Pathology of Malignant Lymphomas. 102: Hodgkin Disease. 103: Lymphomas. 104: Plasma Cell Neoplasms: General Considerations. 105: Essential Monoclonal Gammopathy. 106: Plasma Cell Myeloma. 107: Amyloidosis. 108: Macroglobulinemia. 109: Heavy- Chain Disease. Part X: Hemostatasis and Thrombosis. 110: Megakaryopoiesis and Thrombopoiesis. 111: Platelet Morphology, Biochemistry and Function. 112: Molecular Biology, Biochemistry and Life- Span of Plasma... The Pathway of Blood Coagulation. 113: Control of Coagulation Reactions. 114: Vascular Function in Hemostasis. 115: Evaluation, Classification and Clinical Manifestations of Disorders of Hemos. 116: Molecular Mechanisms of Fibrinolysis. 117: Thrombocytopenia. 118: Thrombocytosis and Essential Thrombocythemia. 119: Hereditary Qualitative Platelet Disorders. 120: Acquired Qualitative Platelet Disorders Due to Disease, Drugs, and Foods. 121: The Vascular Purpuras. 122: Bleeding Disorders Due to Coagulation Factors II, V, VII, X, XI, XIII and Combined FV and VIII. 123: Hemophilia A and Hemophilia B. 124: Hereditary Abnormalities in Fibrinogen. 125: Coagulopathies Associated With Liver Disease, Liver Transplantation. 126: Disseminated Intravascular Coagulation. 127: The Inherited Thrombophilias. 128: Lupus Anticoagulants and Related Disorders. 129: Venous Thrombosis. 130: Thrombosis, Arteriosclerosis, and Coronary Artery Disease. 131: Antiplatelet Drugs and Therapy. 132: Oral Anticoagulants. 133: Heparin, Hirudin and Related Agents. 134: Fibrinolytic Therapy. 135: Von Willebrand Disease. 136: Disorders of Fibrinolysis and Use of Antifibrinolytic Agents. Part XI: Transfusion Medicine. 137: Erythrocyte Antigens and Antibodies. 138: Human Leukocyte and Platelet Antigens. 139: Blood Procurement and Screening. 140: Preservation and Clinical Use of Erythrocytes and Whole Blood. 141: Collection and Transfusion of Leukocytes, Dendritic Cells, and Stem Cells. 142: Preservation and Clinical Use of Platelets. 143: Preparation and Clinical Use of Plasma and Plasma Fractions. 144: Therapeutic Hemapheresis: Indications, Efficacy, Complications.