Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ 0 thalassemia phenotypes
Ikwuanusi, Ifeanyi, Jordan, Lori C., Lee, Chelsea A., Patel, Niral J., Waddle, Spencer, Pruthi, Sumit, Davis, L. Taylor, Griffin, Allison, DeBaun, Michael R., Kassim, Adetola A., Donahue, Manus J.Journal:
American Journal of Hematology
DOI:
10.1002/ajh.25698
Date:
December, 2019
File:
PDF, 280 KB
2019