Researchers sought to determine whether stored electronic health record data would be helpful for creating an automated contemporaneous cohort to estimate survival following disease-modifying treatment in SCA.
Researchers sought to determine whether treatment with hydroxyurea would be cost-effective for children with SCA in sub-Saharan Africa.
Researchers sought to determine reasons for the association of SCD with rates of alloimmunization following transfusion therapy in both high-income and low-income countries.
Researchers sought to determine whether hydroxyurea would be effective for preventing malaria infection in children with SCA living in sub-Saharan Africa.
Majority of youth in Michigan and New York with sickle cell anemia did not have filled hydroxyurea prescriptions.
Researchers assessed whether daily zinc supplementation prevents severe or invasive infection among children with sickle cell anemia.
Researchers sought to determine if there is a link between globin gene regulation and hypoxia adaptation that could impact treatment approaches for thalassemia and SCD.
The 2022 CDC Clinical Practice Guideline is intended to help clinicians weigh the benefits and risks of opioids and alternative pain treatments for outpatients.
Researchers sought to determine whether early initiation of DMT in childhood would prevent myocardial fibrosis in patients with sickle cell anemia.
Researchers sought to determine whether silent cerebral infarctions were associated with cognitive performance or impairment among patients SCA.
