Wintrobe's clinical hematology. Twovolume set + companion website (12th Ed.)
Auteurs : GREER J.P., ARBER D, FORESTER J, BERTIL MD
VOLUME 1
- CH 1. Examination of the Blood and Bone Marrow
- CH 2. Clinical Flow Cytometry
- CH 3. Cytogenetics
- CH 4. Molecular Biology and Hematology
- CH 5. Origin and Development of Blood Cells
- CH 6. Erythropoiesis
- CH 7. The Mature Erythrocyte
- CH 8. Destruction of Erythrocytes
- CH 9. Neutrophilic Leukocytes
- CH 10. The Human Eosinophil
- CH 11. Basophilic Leukocytes: Mast Cells and Basophils
- CH 12. Mononuclear Phagocytes
- CH 13. Phagocytosis
- CH 14. Lymphocytes and Lymphatic Organs
- CH 15. B Lymphocytes
- CH 16. T Lymphocytes and Natural Killer Cells
- CH 17. Effector Mechanisms in Immunity
- 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
- 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
- CH 26. Anemia: General Considerations
- CH 27. Iron Deficiency and Related Disorders
- CH 28. Sideroblastic Anemias
- CH 29. Hemochromatosis
- CH 30. Porphyria
- 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
- 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
- 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
PART I Laboratory Hematology
PART II The Normal Hematologic System
Section 1. Hematopoiesis
Section 2. The Erythrocyte
Section 3. Granulocytes and Monocytes
Section 4. The Lymphocytes
Section 5. Hemostasis
PART III Therapeutic Modalities
PART IV Disorders of Red Cells
Section 1. Introduction
Section 2. Disorders of Iron Metabolism and Heme Synthesis
Section 3. Hemolytic Anemia
Section 4. Hereditary Disorders of Hemoglobin Structure and Synthesis
Section 5. Other Red Cells Disorders
V O L U M E 2
PART V Disorders of Hemostasis and Coagulation
Section 1. Introduction
Section 2. Thrombocytopenia
Section 3. Other Disorders of Primary Hemostasis
Section 4. Coagulation Disorders Platelet Destruction
Section 5 Thrombosis
PART VI Nonmalignant Disorders of Leukocytes,the Spleen, and/or Immunoglobins
PART VII Hematologic Malignancies
Section 1. General
'This is the 12th and most complete iteration of Wintrobe's Clinical Hematology, first published in 1942 by Maxwell Meyer Wintrobe, a leading hematologist at that time. In the years since, the book has been updated, the science elaborated, and the number of editors expanded. Yet subsequent editions have retained the strength of the first edition....The current editorial team consists of the 5 experts who edited the previous edition, along with 2 new editors. All are experts in pediatric or adult hematology/hematopathology, and all are locate
Date de parution : 06-2009
Ouvrage de 3232 p.
21x28 cm
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Wintrobe's Clinical Hematology 412,37 €
