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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 Donahue
Published in: American journal of hematology (2019)
Keyphrases
  • sickle cell disease
  • subarachnoid hemorrhage
  • cerebral ischemia
  • red blood cell
  • brain injury
  • cerebral blood flow
  • blood brain barrier