Wintrobe’s Clinical Hematology 15th Edition Test Bank

This is NOT a textbook. A test bank is a collection of exam questions to provide a resource for students and instructors to create questions that align with the content, learning objectives, and competencies outlined in the textbook or course curriculum.

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Wintrobe’s Clinical Hematology 15th Edition Test Bank
Nursing Test Bank
  • CH 1. Examination of the Blood and Bone Marrow
  • CH 2. Clinical Flow Cytometry
  • CH 3. Cytogenetics
  • CH 4. Molecular Biology and Hematology
  • PART II The Normal Hematologic System
  •  
  • Section 1. Hematopoiesis
  •  
  • CH 5. Origin and Development of Blood Cells
  • Section 2. The Erythrocyte
  •  
  • CH 6. Erythropoiesis
  • CH 7. The Mature Erythrocyte
  • CH 8. Destruction of Erythrocytes
  • Section 3. Granulocytes and Monocytes
  •  
  • CH 9. Neutrophilic Leukocytes
  • CH 10. The Human Eosinophil
  • CH 11. Basophilic Leukocytes: Mast Cells and Basophils
  • CH 12. Mononuclear Phagocytes
  • CH 13. Phagocytosis
  • Section 4. The Lymphocytes
  •  
  • CH 14. Lymphocytes and Lymphatic Organs
  • CH 15. B Lymphocytes
  • CH 16. T Lymphocytes and Natural Killer Cells
  • CH 17. Effector Mechanisms in Immunity
  • Section 5. Hemostasis
  •  
  • CH 18. Megakaryocytes
  • CH 19. Platelet Structure and Function in Hemostasis and Thrombosis
  • CH 20. Blood Coagulation and Fibrinolysis
  • CH 21. Endothelium: Angiogenesis and the Regulation of Hemostasis
  • PART III Therapeutic Modalities
  •  
  • CH 22. Red Cell, Platelet, and White Cell Antigens
  • CH 23. Transfusion Medicine
  • CH 24. Hematopoietic Stem Cell Transplantation
  • CH 25. Gene Therapy for Hematologic Disorders
  • PART IV Disorders of Red Cells
  •  
  • Section 1. Introduction
  •  
  • CH 26. Anemia: General Considerations
  • Section 2. Disorders of Iron Metabolism and Heme Synthesis
  •  
  • CH 27. Iron Deficiency and Related Disorders
  • CH 28. Sideroblastic Anemias
  • CH 29. Hemochromatosis
  • CH 30. Porphyria
  • Section 3. Hemolytic Anemia
  •  
  • CH 31. Hereditary Spherocytosis, Hereditary Elliptocytosis, and Other Disorders Associated with Abnormalities of the Erythrocyte Membrane
  • CH 32. Hereditary Hemolytic Anemias Due to Red Blood Cell Enzyme Disorders
  • CH 33. Autoimmune Hemolytic Anemia
  • CH 34. Alloimmune Hemolytic Disease of the Fetus and Newborn
  • CH 35. Paroxysmal Nocturnal Hemoglobinuria
  • CH 36. Acquired Nonimmune Hemolytic Disorders
  • Section 4. Hereditary Disorders of Hemoglobin Structure and Synthesis
  •  
  • CH 37. Sickle Cell Anemia and Other Sickling Syndromes
  • CH 38. Thalassemias and Related Disorders: Quantitative Disorders of Hemoglobin Synthesis
  • CH 39. Hemoglobins with Altered Oxygen Affinity, Unstable Hemoglobins, M-Hemoglobins, and Dyshemoglobinemias
  • Section 5. Other Red Cells Disorders
  •  
  • CH 40. Megaloblastic Anemias: Disorders of Impaired DNA Synthesis
  • CH 41. Inherited Aplastic Anemia Syndromes
  • CH 42. Acquired Aplastic Anemia
  • CH 43. Red Cell Aplasia
  • CH 44. Congenital Dyserythropoietic Anemias
  • CH 45. Anemias Secondary to Chronic Disease and Systemic Disorders
  • CH 46. Anemias During Pregnancy and the Postpartum Period
  • CH 47. Anemias Unique to the Newborn Period
  • CH 48. Erythrocytosis
ISBN-13

9781975184698

Edition

15th Edition

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