دانلود کتاب هماتولوژی ویلیامز: گلبول قرمز و بیماری های آن
Williams Hematology: The Red Cell and Its Diseases, 1ed

Williams Hematology: The Red Cell and Its Diseases Everything you need to know about red cell disorders, from basic science to clinical application.

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. There are myriad red cell disorders, such as iron deficiency anemia, pernicious anemia, aplastic anemia, autoimmune hemolytic anemia, sickle cell, thalassemia and other hemoglobinopathies.

Williams Hematology: The Red Cell 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. Presented in an accessible template format, the book includes classifications, etiology and pathogenesis, clinical and laboratory features, differential diagnosis, treatment, management, and supportive care.

In this volume, we bring to the reader the most up-to-date consideration of the structure and function of the red cell. After two introductory chapters on the structure and biology of the red cell and erythropoiesis, the focus turns to the comprehensive set of diseases, either acquired or inherited, in which a quantitative (deficiency or excess) or qualitative (membrane, enzyme, hemoglobin) abnormality of the red cell results in disease.

This comprehensive, yet concise resource covers:

• Structure and physiology of the red cell
• Classification of red cell diseases
• Diseases of red cell production
• Anemias resulting principally from inherited disorders
• Anemia as a result of exogenous factors
• Polyclonal erythrocytosis
• Red cell transfusion

Contents

Part I Structure and Physiology of the Red Cell
Part II Classification of Red Cell Diseases
PART III Diseases of Red Cell Production
Part IV Anemias Resulting Principally from Inherited Disorders
Part V Anemia as a Result of Exogenous Factors
Part VI Polyclonal Erythrocytosis
Part VII Red Cell Transfusion