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010 _a2004055200
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_2Uk
020 _a0071435913
020 _a9780071435918
035 _a(OCoLC)55955722
040 _aDNLM/DLC
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049 _aVWEN
050 0 4 _aRC633
_b.H43 2006
060 0 0 _a2005 N-880
060 1 0 _aWH 100
_bW721 2006
082 0 0 _a616.1/5
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099 _aWH
_a100
_aW721
_a2006
245 0 0 _aWilliams hematology
_ceditors, Marshall A. Lichtman ... [et al.].
246 3 0 _aHematology
250 _a7th ed.
260 _aNew York
_bMcGraw-Hill, Medical Pub. Division
_cc2006.
300 _axxvii, 2189, 108 p.
_bill.
_c28 cm.
504 _aIncludes bibliographical references and index.
505 0 0 _tApproach to the patient --
_tExamination of the blood --
_tExamination of the marrow --
_tThe marrow and hematopoietic microenvironment --
_tThe lymphoid tissues --
_tHematology of the newborn --
_tHematology during pregnancy --
_tHematology in the aged --
_tGenetic principles and molecular biology --
_tCytogenetics and gene rearrangement --
_tApoptosis --
_tCell cycle regulation --
_tSignal transduction pathways --
_tThe cluster of differentiation (CD) antigens --
_tHematopoietic stem cells, progenitor cells, and cytokines --
_tThe inflammatory response --
_tThe innate immune system --
_tThe adaptive immune system and dendritic cells --
_tPharmacology and toxicity of antineoplastic drugs --
_tTreatment of infections in the immunocompromised host --
_tPrinciples of antithrombotic therapy --
_tPrinciples of hematopoietic stem cell transplantation --
_tPrinciples of immune cell therapy --
_tPrinciples of vaccine therapy --
_tPrinciples of therapeutic apheresis --
_tPrinciples of gene transfer for therapy --
_tPain management --
_tMorphology of the erythron --
_tComposition of the erythrocyte --
_tProduction of erythrocytes --
_tDestruction of erythrocytes --
_tClinical manifestations and classification of erythrocyte disorders --
_tAplastic anemia --
_tPure red cell aplasia --
_tAnemia of chronic renal disease --
_tAnemia of endocrine disorders --
_tThe congenital dyserythropoietic anemias --
_tParoxysmal nocturnal hemoglobinuria --
_tDisorders of folic acid and cobalamin metabolism: the megaloblastic anemias --
_tDisorders of iron metabolism --
_tAnemia resulting from other nutritional deficiencies --
_tAnemia associated with marrow infiltration --
_tAnemia of chronic disease --
_tDisorders of the red cell membrane: hereditary spherocytosis, elliptocytosis, and related disorders --
_tDisorders of red cells resulting from enzyme abnormalities --
_tDisorders of globin synthesis: the thalassemias --
_tDisorders of hemoglobin structure: sickle cell anemia and related abnormalities --
_tMethemoglobinemia and other causes of cyanosis --
_tHemolytic anemia resulting from physical injury to red cells --
_tHemolytic anemia due to chemical and physical agents --
_tHemolytic anemia due to infections with microorganisms --
_tHemolytic anemia due to immune injury --
_tAlloimmune hemolytic disease of the newborn --
_tAcute blood loss anemia --
_tHypersplenism and hyposplenism vPrimary and secondary polycythemia (Erythrocytosis) --
_tThe hematologic aspects of porphyria --
_tHereditary and acquired sideroblastic anemias --
_tMorphology of neutrophils, eosinophils, and basophils --
_tComposition of neutrophils --
_tProduction, distribution, and fate of neutrophils --
_tEosinophils and their disorders vBasophils and mast cells, and their disorders --
_tClassification and clinical manifestations of neutrophil disorders --
_tNeutropenia and neutrophilia --
_tDisorders of neutrophil function --
_tMorphology of monocytes and macrophages --
_tBiochemistry and function of monocytes and macrophages --
_tProduction, distribution, and fate of monocytes and macrophages --
505 0 0 _tClassification and clinical manifestations of disorders of monocytes and macrophages --
_tMonocytosis and monocytopenia --
_tInflammatory and malignant histiocytosis --
_tLipid storage diseases --
_tMorphology of lymphocytes and plasma cells --
_tComposition and biochemistry of lymphocytes and plasma cells --
_tLymphopoiesis --
_tFunctions of B lymphocytes and plasma cells in immunoglobin --
_tFunctions of T lymphocytes: T-cell receptors for antigen --
_tFunctions of natural killer cells --
_tClassification and clinical manifestations of lymphocytosis and plasma cell disorders --
_tLymphocytosis and lymphocytopenia --
_tImmunodeficiency diseases --
_tAcquired immunodeficiency syndrome (AIDS) --
_tMononucleosis syndromes --
_tClassification and clinical manifestations of the clonal myeloid disorders --
_tMyelodysplastic disorders (Clonal cytopenias and oligoblastic leukemia) --
_tAcute myelogenous leukemia --
_tChronic myelogenous leukemia and related disorders --
_tIdiopathic myelofibrosis (agnogenic myeloid metaplasia) --
_tClassification of malignant lymphoid disorders --
_tAcute lymphocytic leukemia --
_tChronic lymphocytic leukemia and related diseases --
_tHairy cell leukemia --
_tLarge granular lymphocytic leukemia --
_tPathology of malignant lymphomas --
_tThe non-Hodgkin lymphomas --
_tHodgkin lymphoma --
_tPlasma cell neoplasms: General considerations --
_tEssential monoclonal gammopathies --
_tPlasma cell myeloma --
_tAmyloidosis --
_tMacroglobulinemia --
_tHeavy-chain disease --
_tMegakaryopoiesis and thrombopoiesis --
_tPlatelet morphology, biochemistry and function --
_tMolecular biololgy and biochemistry of the coagulation factors and pathways of hemostasis --
_tControl of coagulation reactions --
_tVascular function in hemostasis --
_tClassification, clinical manifestations and evaluation of disorders of hemostasis --
_tThrombocytopenia --
_tThrombocytosis and essential thrombocythemia --
_tHereditary qualitative platelet disorders --
_tAcquired qualitative platelet disorders --
_tThe vascular purpuras --
_tHemophilia A and hemophilia B --
_tInherited deficiencies of coagulation factors II, V, VII, XI and XIIIa --
_tHereditary abnormalities of fibrinogen --
_tvon Willebrand disease --
_tAntibody-mediated coagulation factor deficiencies --
_tHemostatic dysfunction related to liver diseases and liver transplantation --
_tDisseminated intravascular coagulation --
_tHereditary thrombophilias --
_tThe antiphospholipid syndrome --
_tAntibody-mediated thrombotic disorders: thrombotic thrombocytopenia purpura and heparin induced thrombocytopenia --
_tVenous thrombosis --
_tArterial thrombosis --
_tFibrinolysis and thrombolysis --
_tErythrocyte antigens and antibodies --
_tHuman leukocyte and platelet antigens --
_tBlood procurement and screening --
_tPreservation and clinical use of erythrocytes and whole blood --
_tPreservation and clinical use of platelets.
650 0 _aBlood
_xDiseases.
650 0 _aHematology.
650 1 2 _aHematologic Diseases.
700 1 _aLichtman, Marshall A.
700 1 _aWilliams, William J.
_q(William Joseph)
_d1926-
852 _d2010-02-23
852 _d2010-02-23
856 4 1 _3Table of contents only
_uhttp://www.loc.gov/catdir/enhancements/fy0618/2004055200-t.html
856 4 2 _3Contributor biographical information
_uhttp://www.loc.gov/catdir/enhancements/fy0737/2004055200-b.html
942 _2lcc
_cBK