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Title Williams hematology / [edited by] Kenneth Kaushansky, Marshall A. Lichtman, Josef T. Prchal, Marcel Levi, Oliver W. Press, Linda J. Burns, Michael A. Caligiuri.

Publication Info. New York : McGraw-Hill, [2015]
©2016

Copies

Location Call No. Status
 University of Saint Joseph: Pope Pius XII Library - Internet  WORLD WIDE WEB E-BOOK MCGRAW    Downloadable
University of Saint Joseph patrons, please click here to access this McGraw-Hill resource
Edition 9th edition.
Description 1 online resource : color illustrations
Note Preceded by Williams hematology / editors, Kenneth Kaushansky [and others]. 8th ed. c2010.
Bibliography Includes bibliographical references.
Contents Part I: Clinical Evaluation of the Patient -- Chapter 1: Initial Approach to the Patient: History and Physical Examination -- Chapter 2: Examination of Blood Cells -- Chapter 3: Examination of the Marrow -- Chapter 4: Consultative Hematology -- Part II: The Organization of the Lymphohematopoietic Tissues -- Chapter 5: Structure of the Marrow and the Hematopoietic Microenvironment -- Chapter 6: The Organization and Structure of Lymphoid Tissues -- Part III: Epochal Hematology -- Chapter 7: Hematology of the Fetus and Newborn -- Chapter 8: Hematology During Pregnancy -- Chapter 9: Hematology in Older Persons -- Part IV: Molecular and Cellular Hematology -- Chapter 10: Genetic Principles and Molecular Biology -- Chapter 11: Genomics -- Chapter 12: Epigenetics -- Chapter 13: Cytogenetics and Genetic Abnormalities -- Chapter 14: Metabolism of Hematologic Neoplastic Cells -- Chapter 15: Apoptosis Mechanisms: Relevance to the Hematopoietic System -- Chapter 16: Cell-Cycle Regulation and Hematologic Disorders -- Chapter 17: Signal Transduction Pathways -- Chapter 18: Hematopoietic Stem Cells, Progenitors, and Cytokines -- Chapter 19: The Inflammatory Response -- Chapter 20: Innate Immunity -- Chapter 21: Dendritic Cells and Adaptive Immunity -- Part V: Therapeutic Principles -- Chapter 22: Pharmacology and Toxicity of Antineoplastic Drugs -- Chapter 23: Hematopoietic Cell Transplantation -- Chapter 24: Treatment of Infections in the Immunocompromised Host -- Chapter 25: Principles of Antithrombotic Therapy -- Chapter 26: Immune Cell Therapy -- Chapter 27: Vaccine Therapy -- Chapter 28: Therapeutic Apheresis: Indications, Efficacy, and Complications -- Chapter 29: Gene Therapy for Hematologic Diseases -- Chapter 30: Regenerative Medicine: Multipotential Cell Therapy for Tissue Repair -- Part VI: The Erythrocyte -- Chapter 31: Structure and Composition of the Erythrocyte -- Chapter 32: Erythropoiesis -- Chapter 33: Erythrocyte Turnover -- Chapter 34: Clinical Manifestations and Classification of Erythrocyte Disorders -- Chapter 35: Aplastic Anemia: Acquired and Inherited -- Chapter 36: Pure Red Cell Aplasia -- Chapter 37: Anemia of Chronic Disease -- Chapter 38: Erythropoietic Effects of Endocrine Disorders -- Chapter 39: The Congenital Dyserythropoietic Anemias -- Chapter 40: Paroxysmal Nocturnal Hemoglobinuria -- Chapter 41: Folate, Cobalamin, and Megaloblastic Anemias -- Chapter 42: Iron Metabolism -- Chapter 43: Iron Deficiency and Overload -- Chapter 44: Anemia Resulting from other Nutritional Deficiencies -- Chapter 45: Anemia Associated with Marrow Infiltration -- Chapter 46: Erythrocyte Membrane Disorders -- Chapter 47: Erythrocyte Enzyme Disorders -- Chapter 48: The Thalassemias: Disorders of Globin Synthesis -- Chapter 49: Disorders of Hemoglobin Structure: Sickle Cell Anemia and Related Abnormalities -- Chapter 50: Methemoglobinemia and Other Dyshemoglobinemias -- Chapter 51: Fragmentation Hemolytic Anemia -- Chapter 52: Erythrocyte Disorders as a Result of Chemical and Physical Agents -- Chapter 53: Hemolytic Anemia Resulting from Infections with Microorganisms -- Chapter 54: Hemolytic Anemia Resulting from Immune Injury -- Chapter 55: Alloimmune Hemolytic Disease of the Fetus and Newborn -- Chapter 56: Hypersplenism and Hyposplenism -- Chapter 57: Primary and Secondary Erythrocytoses -- Chapter 58: The Porphyrias -- Chapter 59: Polyclonal and Hereditary Sideroblastic Anemias -- Part VII: Neutrophils, Eosinophils, Basophils, and Mast Cells -- Chapter 60: Structure and Composition of Neutrophils, Eosinophils, and Basophils -- Chapter 61: Production, Distribution, and Fate of Neutrophils -- Chapter 62: Eosinophils and Related Disorders.
Chapter 63: Basophils, Mast Cells, and Related Disorders -- Chapter 64: Classification and Clinical Manifestations of Neutrophil Disorders -- Chapter 65: Neutropenia and Neutrophilia -- Chapter 66: Disorders of Neutrophil Function -- 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 Tlymphocytes: T-Cell Receptors for Antigen -- Chapter 77: Functions of Natural Killer Cells -- Chapter 78: Classification and Clinical Manifestations of Lymphocyte and Plasma Cell Disorders -- Chapter 79: Lymphocytosis and Lymphocytopenia -- Chapter 80: Immunodeficiency Diseases -- Chapter 81: Hematologic Manifestations of Acquired Immunodeficiency Syndrome -- Chapter 82: Mononucleosis Syndromes -- Part X: Malignant Myeloid Diseases -- Chapter 83: Classification and Clinical Manifestations of the Clonal Myeloid Disorders -- Chapter 84: Polycythemia Vera -- Chapter 85: Essential Thrombocythemia -- Chapter 86: Primary Myelofibrosis -- Chapter 87: Myelodysplastic Syndromes -- Chapter 88: Acute Myelogenous Leukemia -- Chapter 89: Chronic Myelogenous Leukemia and Related Disorders -- Part XI: Malignant Lymphoid Diseases -- Chapter 90: Classification of Malignant Lymphoid Disorders -- Chapter 91: Acute Lymphoblastic Leukemia -- Chapter 92: Chronic Lymphocytic Leukemia -- Chapter 93: Hairy Cell Leukemia -- Chapter 94: Large Granular Lymphocytic Leukemia -- Chapter 95: General Considerations for Lymphomas: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease -- Chapter 96: Pathology of Lymphomas -- Chapter 97: Hodgkin Lymphoma -- Chapter 98: Diffuse Large B-Cell Lymphoma and Related Diseases -- Chapter 99: Follicular Lymphoma -- Chapter 100: Mantle Cell Lymphoma -- Chapter 101: Marginal Zone B-Cell Lymphomas -- Chapter 102: Burkitt Lymphoma -- Chapter 103: Cutaneous T-Cell Lymphoma (Mycosis Fungoides and ŠZary Syndrome) -- Chapter 104: Mature T-Cell and Natural Killer Cell Lymphomas -- Chapter 105: Plasma Cell Neoplasms: General Considerations -- Chapter 106: Essential Monoclonal Gammopathy -- Chapter 107: Myeloma -- Chapter 108: Immunoglobulin Light-Chain Amyloidosis -- Chapter 109: Macroglobulinemia -- Chapter 110: Heavy-Chain Disease -- Part XII: Hemostasis and Thrombosis -- Chapter 111: Megakaryopoiesis and Thrombopoiesis -- Chapter 112: Platelet Morphology, Biochemistry, and Function -- Chapter 113: Molecular Biology and Biochemistry of the Coagulation Factors and Pathways of Hemostasis -- Chapter 114: Control of Coagulation Reactions -- Chapter 115: Vascular Function in Hemostasis -- Chapter 116: Classification, Clinical Manifestations, and Evaluation of Disorders of Hemostasis -- Chapter 117: Thrombocytopenia -- Chapter 118: Heparin-Induced Thrombocytopenia -- Chapter 119: Reactive Thrombocytosis -- Chapter 120: Hereditary Qualitative Platelet Disorders -- Chapter 121: Acquired Qualitative Platelet Disorders -- Chapter 122: The Vascular Purpuras -- Chapter 123: Hemophilia A and Hemophilia B -- Chapter 124: Inherited Deficiencies of Coagulation Factors II, V, V+VIII, VII, X, XI, and XIII -- Chapter 125: Hereditary Fibrinogen Abnormalities -- Chapter 126: Von Willebrand Disease -- Chapter 127: Antibody-Mediated Coagulation Factor Deficiencies -- Chapter 128: Hemostatic Alterations in Liver Disease and Liver Transplantation -- Chapter 129: Disseminated Intravascular Coagulation -- Chapter 130: Hereditary Thrombophilia -- Chapter 131: The Antiphospholipid Syndrome -- Chapter 132: Thrombotic Microangiopathies -- 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.
Note Online resource; title from electronic title page (AccessMedicine, viewed on July 28, 2015).
Subject Blood -- Diseases.
Hematology.
Blood -- Diseases. (OCoLC)fst00834579
Hematology. (OCoLC)fst00954904
Hematologie. (NL-LeOCL)078532345
Bloedziekten. (NL-LeOCL)07845560X
Hematologic Diseases. (DNLM)D006402
Hematology -- methods. (DNLM)D006405Q000379
Genre/Form Handboeken (vorm) (NL-LeOCL)088143252
Elektronische boeken. (NL-LeOCL)303983256
Added Author Kaushansky, Kenneth, editor.
Lichtman, Marshall A., editor.
Prchal, Josef T., editor.
Levi, Marcel, editor.
Press, Oliver William, editor.
Burns, Linda J., editor.
Caligiuri, Michael A., editor.
Williams, William J. (William Joseph), 1926-2016.
Added Title Hematology
Other Form: Print version: Williams hematology. Ninth edition. New York : McGraw-Hill, 2015 9780071833004 (OCoLC)909852692
ISBN 9780071833004 (alk. paper)
0071833005 (alk. paper)
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