Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ0 thalassemia phenotypes. Issue 3 (22nd December 2019) - 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.