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, Ghana and Nigeria, Sickle Cell and the Social Sciences is anchored in the discipline of sociology, but draws upon a diverse range of fields;
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, Ghana and Nigeria, Sickle Cell and the Social Sciences is anchored in the discipline of sociology, but draws upon a diverse range of fields;
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; Chapter 1. The Essentials on Sickle Cell Anemia: Guidelines; Chapter 2. Seeking Guidance; Chapter 3. Clinical Trials and Sickle Cell Anemia; PART;
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research and clinical focus Covering the genetic basis of the disease along with the most current work in gene editing, Sickle Cell Disease;
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Sickle cell disease (SCD) is a genetic condition that affects approximately 100,000 people in the United States and millions more globally;
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reviews the search and the development of antisickling herbal drugs in Africa, where Sickle cell disease (SCD) is an endemic. The last chapter;
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Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not;
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with sickle cell disease in the Genome Era. This book offers a comprehensive and timeless account of emerging concepts in clinical and basic;
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topics: Hemophilia; Sickle cell acute chest; Sickle cell drugs; Sickle cell gene therapy; Sickle cell menses and pain; Pediatric DVT; Atypical;
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symptoms like anemia, bacterial infections, stroke, pain, swelling in the hands and feet, etc. The gene defect associated with sickle cell disease;
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Sickle Cell Disease is the most common genetic disease world wide and in the UK. It has marked geographical variation in its distribution;
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me was awareness and knowledge and having the tools to stand up and fight. Lee is a boy who has sickle cell and is going to school and he is faced with;
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Senegalese patients and doctors have played in making sickle cell mild in a social setting where public health priorities and economic austerity;
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system disorders, respiratory problems and painful crises in SCD individuals. This book highlights the role of physiotherapy in sickle cell;
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Central American, and East Indian ancestry can also be affected. The underlying problem involves haemoglobin, a component of the red cells in the;
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Central American, and East Indian ancestry can also be affected. The underlying problem involves haemoglobin, a component of the red cells in the;
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Breaking the Cycle of Pain is a collection of poems, stories, and short essays on Halimat's personal experiences living with sickle cell;
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in this issue include Polymerization and red cell membrane changes; Overview on reperfusion injury in the pathophysiology of SCD; Regulation;
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for blood cells, balances procoagulant and anticoagulant properties of the vessel wall and regulates vascular homeostasis by synthesizing;
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