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005			20250609115957.0
008			160309s2017 nyu bf 001 0 eng
010			_a 2016011463
020			_a9781259642470
020			_a125964247X
035			_a(DNLM)101678575
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050	0	0	_aRC633 _b.L53 2017
060	1	0	_aWH 39
082	0	0	_a616.1/5 _223
245	0	0	_aWilliams manual of hematology / _c[edited by] Marshall A. Lichtman ... [and 5 others].
246	1		_aManual of hematology
250			_aNinth edition.
260			_aNew York: _bMcGraw-Hill Medical, _c2017.
263			_a1611
300			_aix, 656 p. : _c23 cm. _bill. (col.)
504			_aIncludes bibliographical references and index.
505			_aMachine generated contents note: 1.Approach to the Patient 2.Classification of Anemias and Polycythemias 3.Aplastic Anemia: Acquired and Inherited 4.Pure Red Cell Aplasia 5.Anemia of Chronic Renal Disease 6.Anemia of Endocrine Disorders 7.Congenital Dyserythropoietic Anemias 8.The Megaloblastic Anemias 9.Iron-Deficiency Anemia and Iron Overload 10.Anemia Resulting from Other Nutritional Deficiencies 11.Hereditary and Acquired Sideroblastic Anemias 12.Anemia Resulting from Marrow Infiltration 13.Anemia of Chronic Inflammation 14.Hereditary Spherocytosis, Elliptocytosis, and Related Disorders 15.Hemolytic Anemia Related to Red Cell Enzyme Defects 16.The Thalassemias 17.The Sickle Cell Diseases and Related Disorders 18.Hemoglobinopathies Associated with Unstable Hemoglobin 19.Methemoglobinemia and Other Dyshemoglobinemias Note continued: 20.Traumatic Hemolytic Anemia, March and Sports-Related Hemoglobinuria, Traumatic Cardiac Hemolytic Anemia 21.Microangiopathic Hemolytic Anemia 22.Hemolytic Anemia Resulting from a Chemical or Physical Agent 23.Hemolytic Anemia Resulting from Infectious Agents 24.Hemolytic Anemia Resulting from Warm-Reacting Antibodies 25.Cryopathic Hemolytic Anemia 26.Drug-Induced Hemolytic Anemia 27.Alloimmune Hemolytic Disease of the Newborn 28.Hypersplenism and Hyposplenism 29.Polyclonal Polycythemias (Primary and Secondary) 30.The Porphyrias 31.Classification and Clinical Manifestations of Neutrophil Disorders 32.Neutropenia and Neutrophilia 33.Disorders of Neutrophil Functions 34.Eosinophils and Their Diseases 35.Basophils and Mast Cells and Their Diseases 36.Monocytosis and Monocytopenia 37.Inflammatory and Malignant Histiocytosis 38.Lipid Storage Disease Note continued: 39.Pharmacology and Toxicity of Antineoplastic Drugs 40.Principles of Hematopoietic Stem Cell Transplantation 41.Classification and Clinical Manifestations of the Clonal Myeloid Disorders 42.Myelodysplastic Syndromes (Clonal Cytopenias and Oligoblastic Myelogenous Leukemia) 43.Polycythemia Vera 44.Primary and Familial Thrombocythemia 45.Paroxysmal Nocturnal Hemoglobinuria (PNH) 46.The Acute Myelogenous Leukemias 47.The Chronic Myelogenous Leukemias 48.Primary Myelofibrosis 49.Classification of the Polyclonal Lymphoid Disorders 50.Lymphocytosis and Lymphocytopenia 51.Primary Immunodeficiency Syndrome 52.The Acquired Immunodeficiency Syndrome 53.The Mononucleosis Syndromes 54.Classification and Clinical Manifestations of the Malignant Lymphoid Disorders 55.The Acute Lymphocytic Leukemias 56.The Chronic Lymphocytic Leukemias 57.Hairy Cell Leukemia 58.Large Granular Lymphocytic Leukemia Note continued: 59.Hodgkin Lymphoma 60.General Considerations of Lymphoma: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease 61.Diffuse Large B-Cell Lymphoma 62.Follicular Lymphomas 63.Mantle Cell Lymphomas 64.Marginal Zone B-Cell Lymphoma 65.Burkitt Lymphoma 66.Cutaneous T-Cell Lymphoma (Mycosis Fungoides and Sezary Syndrome) 67.Mature T-Cell and Natural Killer Cell Lymphomas 68.Essential Monoclonal Gammopathy 69.Myeloma 70.Macroglobulinemia 71.Heavy-Chain Diseases 72.Amyloidosis 73.Clinical Manifestations, Evaluation, and Classification of Disorders of Hemostasis 74.Thrombocytopenia 75.Reactive (Secondary) Thrombocytosis 76.Hereditary Platelet Disorders 77.Acquired Platelet Disorders 78.The Vascular Purpuras 79.Hemophilia A and B 80.von Willebrand Disease 81.Hereditary Disorders of Fibrinogen Note continued: 82.Inherited Deficiencies of Coagulation Factors II, V, VII, X, XI, and XIII and the Combined Deficiencies of Factors V and VIII and of the Vitamin K-Dependent Factors 83.Antibody-Mediated Coagulation Factor Deficiencies 84.Hemostatic Dysfunction Related to Liver Diseases 85.The Antiphospholipid Syndrome (Lupus Anticoagulant and Related Disorders) 86.Disseminated Intravascular Coagulation 87.Fibrinolysis and Thrombolysis 88.Principles of Antithrombotic Therapy 89.Hereditary Thrombophilia 90.Venous Thromboembolism 91.Antibody-Mediated Thrombotic Disorders: Thrombotic Thrombocytopenic Purpura and Heparin-Induced Thrombocytopenia 92.Red Cell Transfusion 93.Transfusion of Platelets 94.Therapeutic Hemapheresis
650	1	2	_aHematologic Diseases _928342
655		2	_aHandbooks _98263
700	1		_aLichtman, Marshall A., _eeditor. _928343
730	0		_aWilliams hematology. _sNinth edition. _928344
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