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Book Cover
E-book

Title Williams Hematology / Kenneth Kaushansky, Josef T. Prchal, Linda J. Burns, Marshall A. Lichtman, Marcel Levi, David C. Linch
Edition Tenth Edition
Published New York, N.Y. : McGraw-Hill Education LLC., c2021
Online access available from:
Access Medicine    View Resource Record  

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Description 1 online resource : ill., figs., tables
Series McGraw-Hill's AccessMedicine
McGraw-Hill's AccessMedicine.
Contents Part I: Clinical Evaluation of the Patient -- Chapter 1: Initial Approach to the Patient: History and Physical Examination -- Chapter 2: Examination of Blood and Marrow Cells -- Chapter 3: Consultative Hematology Part II: The Organization of the Lymphohematopoietic Tissues -- Chapter 4: Structure of the Marrow and the Hematopoietic Microenvironment -- Chapter 5: The Organization and Structure of Lymphoid Tissues Part III: Epochal Hematology -- Chapter 6: Hematology of the Fetus and Newborn -- Chapter 7: Hematology During Pregnancy -- Chapter 8: Hematology in Older Persons Part IV: Molecular and Cellular Hematology -- Chapter 9: Genetic Principles and Molecular Biology -- Chapter 10: Genomics and Epigenomics Chapter 11: Cytogenetic and Genetic Abnormalities -- Chapter 12: Application of Big Data and Deep Learning in Hematology -- Chapter 13: Metabolism of Hematologic Neoplastic Cells -- Chapter 14: Cell Death -- Chapter 15: Cell-Cycle Regulation and Hematologic Disorders -- Chapter 16: Signal Transduction Pathways -- Chapter 17: Hematopoietic Stem Cells, Progenitors, and Cytokines -- Chapter 18: The Inflammatory Response -- Chapter 19: Innate Immunity -- Chapter 20: The Biology of Innate Lymphoid Cells and Natural Killer Cells -- Chapter 21: Dendritic Cells and Adaptive Immunity Part V: Therapeutic Principles -- Chapter 22: Immune Checkpoint Inhibitors -- Chapter 23: Immune Cell Therapy: Chimeric Antigen Receptor T-Cell Therapy -- Chapter 24: Immune Cell Therapy: Dendritic Cell and Natural Killer Cell Therapy -- Chapter 25: Vaccine Therapy -- Chapter 26: Gene Therapy for Hematologic Diseases -- Chapter 27: Regenerative Medicine: Induced Pluripotent Stem Cells And Blood Cell Engineering -- Chapter 28: Pharmacology and Toxicity of Antineoplastic Drugs -- Chapter 29: Hematopoietic Stem Cell Transplantation -- Chapter 30: Therapeutic Apheresis: Indications, Efficacy, and Complications -- Chapter 31: Treatment of Infections in the Immunocompromised Host -- Chapter 32: Antithrombotic Therapy Part VI: The Erythrocyte -- Chapter 33: Structure and Composition of the Erythrocyte -- Chapter 34: Erythropoiesis and Red Cell Turnover -- Chapter 35: Clinical Manifestations and Classification of Erythrocyte Disorders -- Chapter 36: Aplastic Anemia: Acquired and Inherited -- Chapter 37: Pure Red Cell Aplasia -- Chapter 38: Anemia of Chronic Disease -- Chapter 39: Erythropoietic Effects of Endocrine Disorders -- Chapter 40: The Hereditary Dyserythropoietic Anemias -- Chapter 41: Paroxysmal Nocturnal Hemoglobinuria -- Chapter 42: Folate, Cobalamin, and Megaloblastic Anemias -- Chapter 43: Iron Metabolism -- Chapter 44: Iron Deficiency and Overload -- Chapter 45: Anemia Resulting from Other Nutritional Deficiencies -- Chapter 46: Anemia Associated with Marrow Infiltration -- Chapter 47: Erythrocyte Membrane Disorders -- Chapter 48: Erythrocyte Enzyme Disorders -- Chapter 49: Thalassemia: A Disorder of Globin Synthesis -- Chapter 50: Disorders of Hemoglobin Structure: Sickle Cell Anemia and Related Abnormalities -- Chapter 51: Methemoglobinemia and Other Dyshemoglobinemias -- Chapter 52: Fragmentation Hemolytic Anemia -- Chapter 53: Erythrocyte Disorders as a Result of Toxic Agents -- Chapter 54: Hemolytic Anemia Resulting from Infections with Microorganisms -- Chapter 55: Hemolytic Anemia Resulting from Immune Injury -- Chapter 56: Alloimmune Hemolytic Disease of the Fetus and Newborn -- Chapter 57: Hypersplenism and Hyposplenism -- Chapter 58: Primary and Secondary Erythrocytoses/Polycythemias -- Chapter 59: The Porphyrias -- Chapter 60: Polyclonal and Hereditary Sideroblastic Anemias Part VII: Neutrophils, Eosinophils, Basophils, and Mast Cells -- Chapter 61: Structure and Composition of Neutrophils, Eosinophils, and Basophils -- Chapter 62: Classification and Clinical Manifestations of Neutrophil Disorders -- Chapter 63: Neutropenia and Neutrophilia -- Chapter 64: Disorders of Neutrophil Function -- Chapter 65: Eosinophils and Their Disorders -- Chapter 66: Basophils and Mast Cells and Their Disorders Part VIII: Monocytes and Macrophages -- Chapter 67: Structure, Receptors, and Functions of Monocytes and Macrophages -- Chapter 68: Production, Distribution, and Activation of Monocytes and Macrophages -- Chapter 69: Classification and Clinical Manifestations of Disorders of Monocytes and Macrophages -- Chapter 70: Monocytosis and Monocytopenia -- Chapter 71: Inflammatory and Malignant Histiocytosis -- Chapter 72: Gaucher Disease and Related Lysosomal Storage Diseases Part IX: Lymphocytes and Plasma Cells -- Chapter 73: The Structure of Lymphocytes and Plasma Cells -- Chapter 74: Lymphopoiesis -- Chapter 75: Functions of B Lymphocytes and Plasma Cells in Immunoglobulin Production -- Chapter 76: Functions of T Lymphocytes: T-Cell Receptors for Antigen -- Chapter 77: Classification and Clinical Manifestations of Lymphocyte and Plasma Cell Disorders -- Chapter 78: Lymphocytosis and Lymphocytopenia -- Chapter 79: Immunodeficiency Diseases -- Chapter 80: Hematologic Manifestations of Human Immunodeficiency Virus and the Acquired Immunodeficiency Syndrome -- Chapter 81: Mononucleosis Syndromes Part X: Malignant Myeloid Diseases -- Chapter 82: Classification and Clinical Manifestations of the Clonal Myeloid Disorders -- Chapter 83: Polycythemia Vera -- Chapter 84: Essential Thrombocythemia -- Chapter 85: Primary Myelofibrosis -- Chapter 86: Myelodysplastic Syndromes -- Chapter 87: Acute Myelogenous Leukemia -- Chapter 88: Chronic Myelogenous Leukemia and Related Disorders Part XI: Malignant Lymphoid Diseases -- Chapter 89: Classification of Malignant Lymphoid Disorders -- Chapter 90: Acute Lymphoblastic Leukemia -- Chapter 91: Chronic Lymphocytic Leukemia -- Chapter 92: Hairy Cell Leukemia -- Chapter 93: Large Granular Lymphocytic Leukemia -- Chapter 94: General Considerations of Lymphomas: Incidence Rates, Etiology, Diagnosis, Staging, and Primary Extranodal Disease -- Chapter 95: Pathology of Lymphomas -- Chapter 96: Hodgkin Lymphoma -- Chapter 97: Diffuse Large B-Cell Lymphoma and Related Diseases -- Chapter 98: Follicular Lymphoma -- Chapter 99: Mantle Cell Lymphoma -- Chapter 100: Marginal Zone B-Cell Lymphomas -- Chapter 101: Burkitt Lymphoma -- Chapter 102: Cutaneous T-Cell Lymphoma (Mycosis Fungoides and Sézary Syndrome) -- Chapter 103: Mature T-Cell and Natural Killer Cell Lymphomas -- Chapter 104: Plasma Cell Neoplasms: General Considerations -- Chapter 105: Essential Monoclonal Gammopathy -- Chapter 106: Myeloma -- Chapter 107: Immunoglobulin Light Chain Amyloidosis -- Chapter 108: Macroglobulinemia -- Chapter 109: Heavy-Chain Disease Part XII: Hemostasis and Thrombosis -- Chapter 110: Megakaryopoiesis and Thrombopoiesis -- Chapter 111: Platelet Morphology, Biochemistry, and Function -- Chapter 112: Molecular Biology and Biochemistry of the Coagulation Factors and Pathways of Hemostasis -- Chapter 113: Control of Coagulation Reactions -- Chapter 114: Vascular Function in Hemostasis -- Chapter 115: Classification, Clinical Manifestations, and Evaluation of Disorders of Hemostasis -- Chapter 116: Thrombocytopenia -- Chapter 117: Heparin-Induced Thrombocytopenia -- Chapter 118: Hereditary and Reactive Thrombocytosis -- Chapter 119: Inherited Platelet Disorders -- Chapter 120: Acquired Qualitative Platelet Disorders -- Chapter 121: The Vascular Purpuras -- Chapter 122: Hemophilia A and Hemophilia B -- Chapter 123: Inherited Deficiencies of Coagulation Factors II, V, V+VIII, VII, X, XI, and XIII -- Chapter 124: Hereditary Fibrinogen Abnormalities -- Chapter 125: VON Willebrand Disease -- Chapter 126: Antibody-Mediated Coagulation Factor Deficiencies -- Chapter 127: Disseminated Intravascular Coagulation -- Chapter 128: Thrombotic Microangiopathies -- Chapter 129: Hemolytic Uremic Syndrome -- Chapter 130: Hemostatic Alterations in Liver Diseases and Liver Transplantation -- Chapter 131: Hereditary Thrombophilia -- Chapter 132: The Antiphospholipid Syndrome -- Chapter 133: Venous Thrombosis -- Chapter 134: Atherothrombosis: Disease Initiation, Progression, and Treatment -- Chapter 135: Fibrinolysis and Thrombolysis Part XIII: Transfusion Medicine -- Chapter 136: Erythrocyte Antigens and Antibodies -- Chapter 137: Human Leukocyte and Platelet Antigens -- Chapter 138: Blood Procurement and Red Cell Transfusion --
Chapter 139: Preservation and Clinical use of Platelets -- Chapter 140: Using Plasma and Plasma Component Therapy
Summary The first edition of Williams Hematology (né Hematology) was published in 1972. This, our 10th edition, represents our continued efforts over one-half century to provide the most current concepts of the genetic basis, pathophysiology, diagnosis, and treatment of hematologic diseases
Bibliography Includes bibliographical references and indexes
Notes Also issued in Online and PDF version
Description based on cover image and table of contents, viewed on December 07, 2020
Subject Hematologic Diseases. 
Hematology -- methods. 
Form Electronic book
Author Kaushansky, Kenneth, editor.
Prchal, Josef T., editor.
Burns, Linda J., editor.
Lichtman, Marshall A., editor.
Levi, Marcel, editor.
Linch, David C., editor.
LC no. 2020031864
ISBN 9781260464122 (e-ISBN)
1260464121 (e-ISBN)
Other Titles Williams Hematology, Tenth Edition