دانلود کتاب Williams Manual of Hematology 10th Edition

فهرست مطالب کتاب Williams Manual of Hematology 10th Edition – (کتاب راهنمای هماتولوژی ویلیامز ویرایش دهم – 2022):

Part I. Initial Clinical Evaluation
1. Approach to the Patient
Part II. Disorders of Red Cells
2. Classification of Anemias and Erythrocytoses
3. Aplastic Anemia: Acquired and Inherited
4. Pure Red Cell Aplasia
5. Anemia of Chronic (Inflammatory, Neoplastic, and Renal) Disease
6. Erythropoietic Effects of Endocrine Disorders
7. Congenital Dyserythropoietic Anemias
8. Folate, Cobalamin, and Megaloblastic Anemias
9. Iron Deficiency and Iron Overload
10. Anemia Resulting from Other Nutritional Deficiencies
11. Hereditary and Acquired Sideroblastic Anemias
12. Anemia Resulting from Marrow Infiltration
13. Erythrocyte Membrane Disorders
14. Hemolytic Anemia Related to Red Cell Enzyme Defects
15. The Thalassemias
16. The Sickle Cell Diseases and Other Hemoglobinopathies
17. Unstable Hemoglobins and Hemoglobins with Altered Oxygen Affinity
18. Methemoglobinemia and Other Dyshemoglobinemias
19. Fragmentation Hemolytic Anemia
20. Hemolytic Anemia Resulting from a Chemical or Physical Agent
21. Hemolytic Anemia Resulting from Infectious Agents
22. Hemolytic Anemia Resulting from Warm-Reacting Antibodies
23. Cryopathic Hemolytic Anemia
24. Drug-Induced Hemolytic Anemia
25. Alloimmune Hemolytic Disease of the Newborn
26. Hypersplenism and Hyposplenism
27. Polyclonal Erythrocytoses (Primary and Secondary)
28. The Porphyrias
Part III. Disorders of Granulocytes
29. Classification and Clinical Manifestations of Neutrophil Disorders
30. Neutropenia and Neutrophilia
31. Disorders of Neutrophil Function
32. Eosinophils and Their Disorders
33. Basophils, Mast Cells and Their Disorders
Part IV. Disorders of Monocytes and Macrophages
34. Classification and Clinical Manifestations of Monocyte and Macrophage Disorders
35. Monocytosis and Monocytopenia
36. Inflammatory and Malignant Histiocytosis
37. Gaucher Disease and Related Lysosomal Storage Diseases
Part V. Principles of Therapy for Neoplastic Hematologic Disorders
38. Pharmacology and Toxicity of Antineoplastic Drugs
39. Principles of Hematopoietic Cell Transplantation
40. Immune Cell Therapy: Genetically Engineered T Cells
Part VI. The Clonal Myeloid Disorders
41. Classification and Clinical Manifestations of the Clonal Myeloid Disorders
42. Polycythemia Vera
43. Essential Thrombocythemia
44. Paroxysmal Nocturnal Hemoglobinuria
45. Myelodysplastic Syndromes
46. The Acute Myelogenous Leukemias
47. The Chronic Myelogenous Leukemias
48. Primary Myelofibrosis
Part VII. The Polyclonal Lymphoid Diseases
49. Classification and Clinical Manifestations of Polyclonal Lymphocyte and Plasma Cell Disorders
50. Lymphocytosis and Lymphocytopenia
51. Primary Immunodeficiency Syndrome
52. Hematologic Manifestations of the Acquired Immunodeficiency Syndrome
53. The Mononucleosis Syndromes
Part VIII. The Clonal Lymphoid and Plasma Cell Diseases
54. Classification and Clinical Manifestations of the Neoplastic Lymphocytic Disorders
55. The Acute Lymphoblastic Leukemias
56. The Chronic Lymphocytic Leukemias
57. Hairy Cell Leukemia
58. Large Granular Lymphocytic Leukemia
59. General Considerations of Lymphoma: Epidemiology, Etiology, Heterogeneity, and Primary Extranodal Disease
60. Hodgkin Lymphoma
61. Diffuse Large B-Cell Lymphoma and Related Diseases
62. Follicular Lymphoma
63. Mantle Cell Lymphoma
64. Marginal Zone B-Cell Lymphoma
65. Burkitt Lymphoma
66. Cutaneous T-Cell Lymphoma
67. Mature T-Cell and Natural Killer Cell Lymphomas
68. Essential Monoclonal Gammopathy
69. Myeloma
70. Macroglobulinemia
71. Heavy-Chain Diseases
72. Amyloidosis
Part IX. Disorders of Platelets and Hemostasis
73. Clinical Manifestations, Evaluation and Classification of Disorders of Hemostasis
74. Thrombocytopenia
75. Hereditary and Reactive (Secondary) Thrombocytosis
76. Hereditary Platelet Disorders
77. Acquired Platelet Disorders
78. The Vascular Purpuras
Part X. Disorders of Coagulation Proteins
79. Hemophilia A and B
80. von Willebrand Disease
81. Hereditary Disorders of Fibrinogen
82. Inherited Deficiencies of Coagulation Factors II, V, VII, X, XI, and XIII and Combined Deficiencies of Factor V and VIII and of Vitamin K–Dependent Factors
83. Antibody-Mediated Coagulation Factor Deficiencies
84. Hemostatic Dysfunction Related to Liver Diseases
85. The Antiphospholipid Syndrome
86. Disseminated Intravascular Coagulation
87. Fibrinolysis and Thrombolysis
Part XI. Thrombosis and Antithrombotic Therapy
88. Principles of Antithrombotic and Antifibrinolytic Therapy
89. Hereditary Thrombophilia
90. Venous Thromboembolism
91. Antibody-Mediated Thrombotic Disorders: Thrombotic Thrombocytopenic Purpura and Heparin-Induced Thrombocytopenia
Part XII. Transfusion and Hemapheresis
92. Red Cell Transfusion
93. Transfusion of Platelets
94. Plasma and Plasma Component Therapy
95. Therapeutic Hemapheresis
Table of Normal Values
Index