| http://www.w3.org/ns/prov#value | - Now, however, as a result of the high quality of care available in comprehensive sickle cell centers, disease-related mortality during childhood has been reduced to 1 to 2 percent.1,2 This remarkable improvement in survival stems mainly from interventions aimed at preventing early deaths from infection and splenic sequestration, as well as the greater use of diseasemodifying therapies (e.g., hydro
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