Williams Manual of Hematology 9th Edition Marshall A. Lichtman Et Al.

Williams Manual of Hematology 9th Edition Marshall A. Lichtman Et Al. – Ebook Instant Download/Delivery ISBN(s): 9781259642470,125964247X, 9780071833011, 0071833013

Product details:

• ISBN 10: 0071833013
• ISBN 13: 9780071833011
• Author: Marshall A. Lichtman Et Al

Publisher’s Note: Products purchased from Third Party sellers are not guaranteed by the publisher for quality, authenticity, or access to any online entitlements included with the product. The world’s most highly regarded reference text on the mechanisms and clinical management of blood diseases A Doody’s Core Title for 2020! Edition after edition, Williams Hematology has guided generations of clinicians, biomedical researchers, and trainees in many disciplines through the origins, pathophysiological mechanisms, and management of benign and malignant disorders of blood cells and coagulation proteins. It is acknowledged worldwide as the leading hematology resource, with editors who are internationally regarded for their research and clinical achievements and authors who are luminaries in their fields. The Ninth Edition of Williams Hematology is extensively revised to reflect the latest advancements in basic science, translational pathophysiology, and clinical practice. In addition to completely new chapters, it features a full-color presentation that includes 700 photographs, 300 of which are new to this edition, and 475 illustrations. Recognizing that blood and marrow cell morphology is at the heart of diagnostic hematology, informative color images of the relevant disease topics are conveniently integrated into each chapter, allowing easy access to illustrations of cell morphology important to diagnosis. Comprehensive in its depth and breath, this go-to textbook begins with the evaluation of the patient and progresses to the molecular and cellular underpinnings of normal and pathological hematology. Subsequent sections present disorders of the erythrocyte, granulocytes and monocytes, lymphocytes and plasma cells, malignant myeloid and lymphoid diseases, hemostasis and thrombosis, and transfusion medicine.

Table contents:

PART I: Clinical Evaluation of the Patient
1. Initial Approach to the Patient: History and Physical Examination
2. Examination of Blood Cells
3. Examination of The Marrow
4. Consultative Hematology
PART II: The Organization of the Lymphohematopoietic Tissues
5. Structure of the Marrow and the Hematopoietic Microenvironment
6. The Organization and Structure of Lymphoid Tissues
PART III: Epochal Hematology
7. Hematology of the Fetus and Newborn
8. Hematology during Pregnancy
9. Hematology in Older Persons
PART IV: Molecular and Cellular Hematology
10. Genetic Principles and Molecular Biology
11. Genomics
12. Epigenetics
13. Cytogenetics and Genetic Abnormalities
14. Metabolism of Hematologic Neoplastic Cells
15. Apoptosis Mechanisms: Relevance to the Hematopoietic System
16. Cell-Cycle Regulation and Hematologic Disorders
17. Signal Transduction Pathways
18. Hematopoietic Stem Cells, Progenitors, and Cytokines
19. The Inflammatory Response
20. Innate Immunity
21. Dendritic Cells and Adaptive Immunity
PART V: Therapeutic Principles
22. Pharmacology and Toxicity of Antineoplastic Drugs
23. Hematopoietic Cell Transplantation
24. Treatment of Infections in The Immunocompromised Host
25. Antithrombotic Therapy
26. Immune Cell Therapy
27. Vaccine Therapy
28. Therapeutic Apheresis: Indications, Efficacy, and Complications
29. Gene Therapy for Hematologic Diseases
30. Regenerative Medicine: Multipotential Cell Therapy for Tissue Repair
PART VI: The Erythrocyte
31. Structure and Composition of the Erythrocyte
32. Erythropoiesis
33. Erythrocyte Turnover
34. Clinical Manifestations and Classification of Erythrocyte Disorders
35. Aplastic Anemia: Acquired and Inherited
36. Pure Red Cell Aplasia
37. Anemia of Chronic Disease
38. Erythropoietic Effects of Endocrine Disorders
39. The Congenital Dyserythropoietic Anemias
40. Paroxysmal Nocturnal Hemoglobinuria
41. Folate, Cobalamin, and Megaloblastic Anemias
42. Iron Metabolism
43. Iron Deficiency and Overload
44. Anemia Resulting from Other Nutritional Deficiencies
45. Anemia Associated with Marrow Infiltration
46. Erythrocyte Membrane Disorders
47. Erythrocyte Enzyme Disorders
48. The Thalassemias: Disorders of Globin Synthesis
49. Disorders of Hemoglobin Structure: Sickle Cell Anemia and Related Abnormalities
50. Methemoglobinemia and Other Dyshemoglobinemias
51. Fragmentation Hemolytic Anemia
52. Erythrocyte Disorders as a Result of Chemical and Physical Agents
53. Hemolytic Anemia Resulting from Infections with Microorganisms
54. Hemolytic Anemia Resulting from Immune Injury
55. Alloimmune Hemolytic Disease of the Fetus and Newborn
56. Hypersplenism and Hyposplenism
57. Primary and Secondary Erythrocytoses
58. The Porphyrias
59. Polyclonal and Hereditary Sideroblastic Anemias
PART VII: Neutrophils, Eosinophils, Basophils, and Mast Cells
60. Structure and Composition of Neutrophils, Eosinophils, and Basophils
61. Production, Distribution, and Fate of Neutrophils
62. Eosinophils and Related Disorders
63. Basophils, Mast Cells, and Related Disorders
64. Classification and Clinical Manifestations of Neutrophil Disorders
65. Neutropenia and Neutrophilia
66. Disorders of Neutrophil Function
PART VIII: Monocytes and Macrophages
67. Structure, Receptors, and Functions of Monocytes and Macrophages
68. Production, Distribution, and Activation of Monocytes and Macrophages
69. Classification and Clinical Manifestations of Disorders of Monocytes and Macrophages
70. Monocytosis and Monocytopenia
71. Inflammatory and Malignant Histiocytosis
72. Gaucher Disease and Related Lysosomal Storage Diseases
PART IX: Lymphocytes and Plasma Cells
73. The Structure of Lymphocytes and Plasma Cells
74. Lymphopoiesis
75. Functions of B Lymphocytes and Plasma Cells in Immunoglobulin Production
76. Functions of T Lymphocytes: T-Cell Receptors for Antigen
77. Functions of Natural Killer Cells
78. Classification and Clinical Manifestations of Lymphocyte and Plasma Cell Disorders
79. Lymphocytosis and Lymphocytopenia
80. Immunodeficiency Diseases
81. Hematologic Manifestations of Acquired Immunodeficiency Syndrome
82. Mononucleosis Syndromes
PART X: Malignant Myeloid Diseases
83. Classification and Clinical Manifestations of the Clonal Myeloid Disorders
84. Polycythemia Vera
85. Essential Thrombocythemia
86. Primary Myelofibrosis
87. Myelodysplastic Syndromes
88. Acute Myelogenous Leukemia
89. Chronic Myelogenous Leukemia and Related Disorders
PART XI: Malignant Lymphoid Diseases
90. Classification of Malignant Lymphoid Disorders
91. Acute Lymphoblastic Leukemia
92. Chronic Lymphocytic Leukemia
93. Hairy Cell Leukemia
94. Large Granular Lymphocytic Leukemia
95. General Considerations for Lymphomas: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease
96. Pathology of Lymphomas
97. Hodgkin Lymphoma
98. Diffuse Large B-Cell Lymphoma and Related Diseases
99. Follicular Lymphoma
100. Mantle Cell Lymphoma
101. Marginal Zone B-Cell Lymphomas
102. Burkitt Lymphoma
103. Cutaneous T-Cell Lymphoma (Mycosis Fungoides and Sézary Syndrome)
104. Mature T-Cell and Natural Killer Cell Lymphomas
105. Plasma Cell Neoplasms: General Considerations
106. Essential Monoclonal Gammopathy
107. Myeloma
108. Immunoglobulin Light-Chain Amyloidosis
109. Macroglobulinemia
110. Heavy-Chain Disease
PART XII: Hemostasis and Thrombosis
111. Megakaryopoiesis and Thrombopoiesis
112. Platelet Morphology, Biochemistry, and Function
113. Molecular Biology and Biochemistry of the Coagulation Factors and Pathways of Hemostasis
114. Control of Coagulation Reactions
115. Vascular Function in Hemostasis
116. Classification, Clinical Manifestations, and Evaluation of Disorders of Hemostasis
117. Thrombocytopenia
118. Heparin-Induced Thrombocytopenia
119. Reactive Thrombocytosis
120. Hereditary Qualitative Platelet Disorders
121. Acquired Qualitative Platelet Disorders
122. The Vascular Purpuras
123. Hemophilia A and Hemophilia B
124. Inherited Deficiencies of Coagulation Factors II, V, V+VIII, VII, X, XI, and XIII
125. Hereditary Fibrinogen Abnormalities
126. von Willebrand Disease
127. Antibody-Mediated Coagulation Factor Deficiencies
128. Hemostatic Alterations in Liver Disease and Liver Transplantation
129. Disseminated Intravascular Coagulation
130. Hereditary Thrombophilia
131. The Antiphospholipid Syndrome
132. Thrombotic Microangiopathies
133. Venous Thrombosis
134. Atherothrombosis: Disease Initiation, Progression, and Treatment
135. Fibrinolysis and Thrombolysis
PART XIII: Transfusion Medicine
136. Erythrocyte Antigens and Antibodies
137. Human Leukocyte and Platelet Antigens
138. Blood Procurement and Red Cell Transfusion
139. Preservation and Clinical Use of Platelets

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