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LEADER: 09459cam 22007694a 4500
001 ocm55955722
003 OCoLC
005 20200929075643.0
008 040706s2006 nyua b 001 0 eng
010 $a 2004055200
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050 00 $aRC633$b.H43 2006
060 00 $aWH 100$bW721 2006
082 00 $a616.1/5$222
084 $a44.86$2bcl
245 00 $aWilliams hematology /$ceditors, Marshall A. Lichtman [and others].
246 30 $aHematology
250 $a7th ed.
260 $aNew York :$bMcGraw-Hill, Medical Pub. Division,$c©2006.
300 $axxvii, 2189, 108 pages :$billustrations ;$c28 cm
336 $atext$btxt$2rdacontent
337 $aunmediated$bn$2rdamedia
338 $avolume$bnc$2rdacarrier
504 $aIncludes bibliographical references and index.
505 00 $tApproach to the patient --$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 00 $tClassification and clinical manifestations of disorders of monocytes and macrophages --$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 --$tMolecular biology and biochemistry of the coagulation factors and pathways of hemostasis --$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.
520 $aThe hematology classic returns with a new editorial team, a new set of expert contributors, and a complete updating of the contents as it continues to define the modern practice of clinical hematology. Look for new chapters on the use of venous access devices, pain management, therapeutic use of cytokines, and flow cytometry. Plus, the latest moelcular biology techniques and 300 color plates enhance your diagnostic skills.
650 0 $aBlood$xDiseases.
650 0 $aHematology.
650 6 $aSang$xMaladies.
650 6 $aHématologie.
650 7 $a44.86 haematology.$0(NL-LeOCL)077596773$2bcl
650 7 $aBlood$xDiseases.$2fast$0(OCoLC)fst00834579
650 7 $aHematology.$2fast$0(OCoLC)fst00954904
650 17 $aHematology.$0(NL-LeOCL)078532345$2gtt
650 17 $aBlood diseases.$0(NL-LeOCL)07845560X$2gtt
650 7 $aDoenças hematológicas.$2larpcal
650 12 $aHematologic Diseases.$0https://id.nlm.nih.gov/mesh/D006402
700 1 $aLichtman, Marshall A.
700 1 $aWilliams, William J.$q(William Joseph),$d1926-2016.
856 41 $3Table of contents$uhttp://catdir.loc.gov/catdir/enhancements/fy0618/2004055200-t.html
856 41 $uhttp://www.accessmedicine.com/resourceTOC.aspx?resourceID=69$zOnline access via AccessMedicine
856 41 $uhttp://online.statref.com/document.aspx?grpalias=UCPSM&fxid=167&docid=1$zOnline access via STAT!Ref
856 42 $3Contributor biographical information$uhttp://catdir.loc.gov/catdir/enhancements/fy0737/2004055200-b.html
938 $aBaker & Taylor$bBKTY$c199.00$d.00$i0071435913$n0006070841$sactive
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