Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ0 thalassemia phenotypes

Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ⁰ thalassemia phenotypes

Am J Hematol. 2020 Mar;95(3):E66-E68. doi: 10.1002/ajh.25698. Epub 2019 Dec 22.

Ifeanyi Ikwuanusi¹, Lori C Jordan^{1

2

3}, Chelsea A Lee^{1

2}, Niral J Patel^{1

2}, Spencer Waddle¹, Sumit Pruthi¹, L Taylor Davis¹, Allison Griffin¹, Michael R DeBaun^{4

5}, Adetola A Kassim⁵, Manus J Donahue^{1

3

6}

¹ Department of Radiology, Vanderbilt University Medical Center, Nashville, Tennessee.
² Department of Pediatrics, Division of Pediatric Neurology, Vanderbilt University Medical Center, Nashville, Tennessee.
³ Department of Neurology, Vanderbilt University Medical Center, Nashville, Tennessee.
⁴ Department of Pediatrics, Vanderbilt-Meharry Center for Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, Tennessee.
⁵ Department of Internal Medicine, Division of Hematology/Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
⁶ Department of Psychiatry, Vanderbilt University Medical Center, Nashville, Tennessee.

No abstract available