Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ0 thalassemia phenotypes.
Ifeanyi IkwuanusiLori C JordanChelsea A LeeNiral J PatelSpencer WaddleSumit PruthiL Taylor DavisAllison GriffinMichael Rutledge DeBaunAdetola A KassimManus J DonahuePublished in: American journal of hematology (2019)