Sickle Cell Anemia
-15%
portes grátis
Sickle Cell Anemia
From Basic Science to Clinical Practice
Costa, Fernando Ferreira; Conran, Nicola
Springer International Publishing AG
04/2018
435
Mole
Inglês
9783319791531
15 a 20 dias
7611
Descrição não disponível.
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 S?
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.
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 S?
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.
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
Hematology;Hemoglobin;Hereditary Disease;Red Cells;Sickle Cell Anemia
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 S?
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.
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 S?
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.
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
