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Sickle Cell Anemia From Basic Science to Clinical Practice /
Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not fully understood. A single mutation in the beta-globin gene incurs numerous molecular and cellular mechanisms that contribute to the plethora of symptoms associated...
| Clasificación: | Libro Electrónico |
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| Autor Corporativo: | |
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Cham :
Springer International Publishing : Imprint: Springer,
2016.
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| Edición: | 1st ed. 2016. |
| Temas: | |
| Acceso en línea: | Texto Completo |
Tabla de Contenidos:
- Chapter 1 Hemoglobin: Structure, Synthesis and Oxygen Transport
- Chapter 2 Sickle cell Anemia: History and Epidemiology
- Chapter 3 Overview of Sickle Cell Anemia Pathophysiology
- Chapter 4 Red Blood Cells and the Vaso-occlusive Process
- Chapter 5 Leukocytes in the vaso-occlusive process
- Chapter 6 Hypercoagulability and Sickle Cell Disease
- Chapter 7 Cardiovascular Adaptations to Anemia and the Role of Vascular Endothelium in Sickle Cell Disease Pathophysiology
- Chapter 8 Inflammation and Sickle Cell Anemia
- Chapter 9 Clinical Manifestations of Sickle Cell Anemia: Infants and Children
- Chapter 10 Treatment of Childhood Sickle Cell Disease
- Chapter 11 Priapism in Sickle Cell Disease: New aspects of pathophysiology
- Chapter 12 Clinical Manifestations and Treatment of Adult Sickle Cell
- Chapter 13 Hemoglobin Sβ Thalassemia, SC Disease and SD Disease: Clinical and Laboratorial Aspects
- Chapter 14 Sickle Cell Disease in Africa and the Arabian Peninsula: Current Management and Challenges
- Chapter 15 Genetic Factors modifying sickle cell disease severity
- Chapter 16 Future Perspectives for the Treatment of Sickle Cell.