Williams Hematology: Red Cell and Its Diseases
DESCRIERE
A comprehensive, much-needed clinical guide to red cell disorders
Red blood cell (RBC) disorders are conditions that affect the red blood cells. When red blood cells do not have enough hemoglobin, oxygen cannot reach all parts of the body—as a result, organs start to malfunction and may lead to a host of issues including deformities, enlarged spleen, heart problems and other diseases. The Red Cells and its Diseases provides clinicians with a practical diagnostic and treatment framework for identifying and successfully managing acute, congenital, and chronic red blood cell disorders. This comprehensive, yet concise resource covers the structure and physiology of the red cell, classification of red cell disease, diseases of red cell production, the causes of anemia, red cell transfusion, and more.
- Market: Hematologists-oncologists (15, 000 US; 25, 000 global), internal medicine (114, 087), internal medicine/pediatrics (4, 840), medical students (3rd year/4th year) (20, 000), nurse practitioners (270, 000), physician assistants (140, 000)
- Fills a gap in the literature on red cell disorders
- Provides new foundations for development of therapy for red cell diseases
- Includes classifications, etiology and pathogenesis, clinical and laboratory features, differential diagnosis, treatment, management, and supportive care
Part 1. Structure and Physiology of the Red Cell |
Chap. 1 Structure of the Red Cell |
Chap 2. Erythropoiesis and Red Cell turnover |
Part 2. Classification of Red cell Diseases |
Chap. 3. Clinical Manifestations and Classification of Red Cell Disorders |
Part 3. Diseases of Red Cell Production |
Chap 4. Aplastic Anemia |
Chap 5. Erythroid Aplasia |
Chap 6. Anemia of Chronic Inflammation |
Chap 7. Erythropoietic effects of endocrine disorders |
Chap 8. Paroxysmal nocturnal hemoglobinuria |
Chap 9. Folate, Cobalamin and the megaloblastic anemia |
Chap 10. Iron Metabolism |
Chap. 11. Iron deficiency anemia |
Chap 12. Anemia resulting from other nutritional deficiencies |
Chap 13. Anemia associated with marrow infiltration |
Part 4. Anemias as a result principally of inherited disorders |
Chap 14. Congenital (inherited) dyserythropoietic anemias |
Chap 15. Erythrocyte membrane disorders |
Chap 16. Erythrocyte Enzyme disorders |
Chap 17. The thalassemias |
Chap 18. Disorders of hemoglobin structure: Sickle cell anemia and related abnormalities |
Chap 19. Methemoglobinemia and other dyhemoglobinemias |
Chap 20. Polyclonal hereditary and acquired sideroblastic anemia |
Chap 21. The porphyrias |
Part 5. Anemia as a result of exogenous factors |
Chap 22. Fragmentation hemolytic anemia |
Chap 23. Erythrocyte disorders as a result of chemicals, metals, and other toxic agents |
Chap 24. Hemolytic anemia as a result of infections with microorganisms |
Chap 25. Hypersplenism and hyposplenism |
Chap 26. Immune hemolytic anemia |
Chap 27. Alloimmune hemolytic disease of the fetus and newborn |
Part 6. Erythrocytosis |
Chap 27. Primary and secondary erythrocytosis |
Part 7. Red Cell Transfusion |
Chap 28. Erythrocyte antigens and antibodies |
Chap 29. Blood procurement and red cell transfusion |
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Marshall A. Lichtman, MD, is dean emeritus, and a former professor of medicine, biochemistry, and biophysics at the University of Rochester Medical Center in New York. He is a past president of the American Society of Hematology (ASH).
Josef T. Prchal, MD, is a professor in the division of hematology and hematologic malignancies, a Huntsman Cancer Institute investigator, and a member of the Cell Response and Regulation Program and the Imaging, Diagnostics, and Therapeutics Program at the University of Utah.
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