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Management of sickle cell disease
BMJ, 2008Hypoxia, hemolysis and infection are more or less associated in patients affected with sickle cell disease. Treatment is based on a programme including regular lifestyle, hydration, folic acid supply, prevention of pneumococcal infections and cerebrovascular events in children, regular follow-up in specialised centres allowing precocious screening and ...
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Fetal Hemoglobin, Sickling, and Sickle Cell Disease
Advances in Pediatrics, 1990Increased numbers of F cells and large amounts of Hb F/F cell appear to produce clinical benefit in rare variants of sickle cell disease and probably in more commonly encountered patients. Fetal hemoglobin interferes with polymerization of Hb S in vitro, but laboratory studies carried out with homogeneous hemoglobin solutions are inadequate models of ...
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Sickle Cell Disease Literature
The Journal of the American Dental Association, 2021Marcia Pereira, Alves Dos Santos +3 more
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Archives of Surgery, 1940
Since the original description of sickle cell anemia by Herrick in 1910,1sufficient data have been accumulated to permit certain statements concerning the pathologic physiology involved and to warrant certain practical conclusions as to the management of the condition.
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Since the original description of sickle cell anemia by Herrick in 1910,1sufficient data have been accumulated to permit certain statements concerning the pathologic physiology involved and to warrant certain practical conclusions as to the management of the condition.
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