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003 | MACHS | ||
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008 | 040706s2006 nyua b 001 0 eng | ||
010 | _a2004055200 | ||
016 | 7 |
_a101223626 _2DNLM |
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016 | 7 |
_a013282471 _2Uk |
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020 | _a0071435913 | ||
020 | _a9780071435918 | ||
035 | _a(OCoLC)55955722 | ||
040 |
_aDNLM/DLC _cDLC _dNLM _dBAKER _dC#P _dMUQ _dJVD _dHU6 _dIG# _dBTCTA _dYDXCP _dUKM _dUBA _dVYD |
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042 | _apcc | ||
049 | _aVWEN | ||
050 | 0 | 4 |
_aRC633 _b.H43 2006 |
060 | 0 | 0 | _a2005 N-880 |
060 | 1 | 0 |
_aWH 100 _bW721 2006 |
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_a616.1/5 _222 |
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_aWH _a100 _aW721 _a2006 |
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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 |