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Williams manual of hematology / [edited by] Marshall A. Lichtman ... [and 5 others].

Contributor(s): Material type: TextTextPublication details: New York: McGraw-Hill Medical, 2017.Edition: Ninth editionDescription: ix, 656 p. : 23 cm. ill. (col.)ISBN:
  • 9781259642470
  • 125964247X
Other title:
  • Manual of hematology
Uniform titles:
  • Williams hematology. Ninth edition.
Subject(s): Genre/Form: DDC classification:
  • 616.1/5 23
LOC classification:
  • RC633 .L53 2017
NLM classification:
  • WH 39
Contents:
Machine 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
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Holdings
Item type Current library Call number Copy number Status Barcode
Books Books Zetech Library - Mang'u Campus General Stacks RC633 .L53 2017 (Browse shelf(Opens below)) C1 Available Z012765
Books Books Zetech Library - Mang'u Campus General Stacks RC633 .L53 2017 (Browse shelf(Opens below)) C2 Available Z012766

Includes bibliographical references and index.

Machine 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

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