Sickle Cell Anemia
From Basic Science to Clinical Practice
Herausgegeben:Costa, Fernando Ferreira; Conran, Nicola
Sickle Cell Anemia
From Basic Science to Clinical Practice
Herausgegeben:Costa, Fernando Ferreira; Conran, Nicola
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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 with the disease. Our knowledge regarding sickle cell disease mechanisms, while still not complete, has broadened considerably over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the disease's pathophysiology…mehr
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- Produktdetails
- Verlag: Springer / Springer International Publishing / Springer, Berlin
- Artikelnr. des Verlages: 86363844, 978-3-319-06712-4
- Seitenzahl: 435
- Erscheinungstermin: 11. April 2016
- Englisch
- Abmessung: 241mm x 160mm x 29mm
- Gewicht: 865g
- ISBN-13: 9783319067124
- ISBN-10: 3319067125
- Artikelnr.: 40707908
- Verlag: Springer / Springer International Publishing / Springer, Berlin
- Artikelnr. des Verlages: 86363844, 978-3-319-06712-4
- Seitenzahl: 435
- Erscheinungstermin: 11. April 2016
- Englisch
- Abmessung: 241mm x 160mm x 29mm
- Gewicht: 865g
- ISBN-13: 9783319067124
- ISBN-10: 3319067125
- Artikelnr.: 40707908
Chapter 2 Sickle cell Anemia: History and Epidemiology.-
Chapter 3 Overviewof Sickle Cell Anemia Pathophysiology.-
Chapter 4 Red Blood Cells and the Vaso-occlusive Process.-
Chapter5 Leukocytes in the vaso-occlusive process.-
Chapter 6 Hypercoagulability andSickle Cell Disease.-
Chapter 7 Cardiovascular Adaptations to Anemia and theRole of Vascular Endothelium in Sickle Cell Disease Pathophysiology.-
Chapter 8Inflammation and Sickle CellAnemia.-
Chapter 9 Clinical Manifestations of Sickle Cell Anemia: Infants and Children.-
Chapter 10 Treatment of Childhood Sickle Cell Disease.-
Chapter 11 Priapism inSickle Cell Disease: New aspects of pathophysiology.-
Chapter 12 ClinicalManifestations and Treatment of Adult Sickle Cell.-
Chapter 13 Hemoglobin SbetaThalassemia, SC Disease and SD Disease: Clinical and Laboratorial Aspects.-
Chapter 14 Sickle Cell Disease in Africa and the Arabian Peninsula: CurrentManagement and Challenges.-
Chapter 15 Genetic Factorsmodifying sickle cell disease severity.-
Chapter 16 Future Perspectives for theTreatment of Sickle Cell.
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.
Chapter 2 Sickle cell Anemia: History and Epidemiology.-
Chapter 3 Overviewof Sickle Cell Anemia Pathophysiology.-
Chapter 4 Red Blood Cells and the Vaso-occlusive Process.-
Chapter5 Leukocytes in the vaso-occlusive process.-
Chapter 6 Hypercoagulability andSickle Cell Disease.-
Chapter 7 Cardiovascular Adaptations to Anemia and theRole of Vascular Endothelium in Sickle Cell Disease Pathophysiology.-
Chapter 8Inflammation and Sickle CellAnemia.-
Chapter 9 Clinical Manifestations of Sickle Cell Anemia: Infants and Children.-
Chapter 10 Treatment of Childhood Sickle Cell Disease.-
Chapter 11 Priapism inSickle Cell Disease: New aspects of pathophysiology.-
Chapter 12 ClinicalManifestations and Treatment of Adult Sickle Cell.-
Chapter 13 Hemoglobin SbetaThalassemia, SC Disease and SD Disease: Clinical and Laboratorial Aspects.-
Chapter 14 Sickle Cell Disease in Africa and the Arabian Peninsula: CurrentManagement and Challenges.-
Chapter 15 Genetic Factorsmodifying sickle cell disease severity.-
Chapter 16 Future Perspectives for theTreatment of Sickle Cell.
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.