Williams obstetrics

INDICE: 1 Approach to the patient. 2 Examination of the blood. 3 Examination of the marrow. 4 The marrow and hematopoietic microenvironment. 5 The lymphoid tissues. 6 Hematology of the newborn. 7 Hematology during pregnancy. 8 Hematology in the aged. 9 Genetic principles and molecular biology. 10 Cytogenetics and gene rearrangement. 11 Apoptosis. 12 Cell cycle regulation. 13 Signal transduction pathways. 14 The cluster of differentiation (CD) antigens. 15 Hematopoietic stem cells, progenitor cells, and cytokines. 16 The inflammatory response. 17 The innate immune system. 18 The adaptive immune system and dendritic cells. 19 Pharmacology and toxicity of antineoplastic drugs. 20 Treatment ofinfections in the immunocompromised host. 21 Principles of antithrombotic therapy. 22 Principles of hematopoietic stem cell transplantation. 23 Principles of immune cell therapy. 24 Principles of vaccine therapy. 25 Principles of therapeutic apheresis. 26 Principles of gene transfer for therapy. 27 Pain management. 28 Morphology of the erythron. 29 Composition of the erythrocyte. 30 Production of erythrocytes. 31 Destruction of erythrocytes. 32 Clinical manifestations and classification of erythrocyte disorders. 33 Aplastic anemia. 34 Purered cell aplasia. 35 Anemia of chronic renal disease. 36 Anemia of endocrine disorders. 37 The congenital dyserythropoietic anemias. 38 Paroxysmal nocturnal hemoglobinuria. 39 Disorders of folic acid and cobalamin metabolism: the megaloblastic anemias. 40 Disorders of iron metabolism. 41 Anemia resulting from other nutritional deficiencies. 42 Anemia associated with marrow infiltration.43 Anemia of chronic disease. 44 Disorders of the red cell membrane: hereditary spherocytosis, elliptocytosis, and related disorders. 45 Disorders of red cells resulting from enzyme abnormalities. 46 Disorders of globin synthesis: the thalassemias. 47 Disorders of hemoglobin structure: sickle cell anemia and related abnormalities. 48 Methemoglobinemia and other causes of cyanosis. 49 Hemolytic anemia resulting from physical injury to red cells. 50 Hemolytic anemia due to chemical and physical agents. 51 Hemolytic anemia due to infections with microorganisms. 52 Hemolytic anemia due to immune injury. 53 Alloimmune hemolytic disease of the newborn. 54 Acute blood loss anemia. 55 Hypersplenism and hyposplenism. 56 Primary and secondary polycythemia (Erythrocytosis). 57 The hematologic aspects of porphyria. 58 Hereditary and acquired sideroblastic anemias. 59 Morphology of neutrophils, eosinophils, and basophils. 60 Composition of neutrophils. 61 Production, distribution, and fate of neutrophils. 62 Eosinophils and their disorders. 63 Basophils and mast cells, and their disorders. 64 Classification and clinical manifestations of neutrophil disorders. 65 Neutropenia and neutrophilia. 66 Disorders of neutrophil function. 67 Morphology of monocytes and macrophages. 68 Biochemistry and function of monocytes and macrophages. 69 Production, distribution, and fate of monocytes and macrophages. 70 Classification and clinical manifestations of disorders of monocytes andmacrophages. 71 Monocytosis and monocytopenia. 72 Inflammatory and malignant histiocytosis. 73 Lipid storage diseases. 74 Morphology of lymphocytes and plasma cells. 75 Composition and biochemistry of lymphocytes and plasma cells. 76Lymphopoiesis. 77 Functions of B lymphocytes and plasma cells in immunoglobin. 78 Functions of T lymphocytes: T-cell receptors for antigen. 79 Functions ofnatural killer cells. 80 Classification and clinical manifestations of lymphocytosis and plasma cell disorders. 81 Lymphocytosis and lymphocytopenia. 82 Immunodeficiency diseases. 83 Acquired immunodeficiency syndrome (AIDS). 84 Mononucleosis syndromes. 85 Classification and clinical manifestations of the clonal myeloid disorders. 86 Myelodysplastic disorders (Clonal cytopenias and oligoblastic leukemia). 87 Acute myelogenous leukemia. 88 Chronic myelogenous leukemia and related disorders. 89 Idiopathic myelofibrosis (agnogenic myeloid metaplasia). 90 Classification of malignant lymphoid disorders. 91 Acute lymphocytic leukemia. 92 Chronic lymphocytic leukemia and related diseases. 93 Hairy cell leukemia. 94 Large granular lymphocytic leukemia. 95 Pathology of malignant lymphomas. 96 The non-Hodgkin lymphomas. 97 Hodgkin lymphoma. 98 Plasma cellneoplasms: General considerations. 99 Essential monoclonal gammopathies. 100 Plasma cell myeloma. 101 Amyloidosis. 102 Macroglobulinemia. 103 Heavy-chain disease. 104 Megakaryopoiesis and thrombopoiesis. 105 Platelet morphology, biochemistry and function. 106 Molecular biololgy and biochemistry of the coagulation factors and pathways of hemostasis. 107 Control of coagulation reactions. 108 Vascular function in hemostasis. 109 Classification, clinical manifestations and evaluation of disorders of hemostasis. 110 Thrombocytopenia. 111 Thrombocytosis and essential thrombocythemia. 112 Hereditary qualitative platelet disorders. 113 Acquired qualitative platelet disorders. 114 The vascular purpuras. 115 Hemophilia A and hemophilia B. 116 Inherited deficiencies of coagulation factors II, V, VII, XI and XIIIa. 117 Hereditary abnormalities of fibrinogen. 118 von Willebrand disease. 119 Antibody-mediated coagulation factor deficiencies. 120 Hemostatic dysfunction related to liver diseases and liver transplantation. 121 Disseminated intravascular coagulation. 122 Hereditary thrombophilias. 123 The antiphospholipid syndrome. 124 Antibody-mediated thrombotic disorders: thrombotic thrombocytopenia purpura and heparin induced thrombocytopenia. 125 Venous thrombosis. 126 Arterial thrombosis. 127 Fibrinolysis and thrombolysis. 128 Erythrocyte antigens and antibodies. 129 Human leukocyte and platelet antigens. 130 Blood procurement and screening. 131 Preservation and clinical use of erythrocytes and whole blood. 132 Preservation and clinical use of platelets.

• ISBN: 978-0-07-149701-5
• Editorial: McGraw-Hill
• Encuadernacion: Cartoné
• Páginas: 1385
• Fecha Publicación: 01/09/2009
• Nº Volúmenes: 1
• Idioma: Inglés