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

Ikwuanusi I, Jordan LC, Lee CA, Patel NJ, Waddle S, Pruthi S, Davis LT, Griffin A, DeBaun MR, Kassim AA, Donahue MJ
Am J Hematol. 2020 95 (3): E66-E68

PMID: 31814164 · PMCID: PMC7017969 · DOI:10.1002/ajh.25698

MeSH Terms (11)

Adolescent Adult Anemia, Sickle Cell Cerebrovascular Circulation Child Female Hemodynamics Hemoglobin, Sickle Humans Male Thalassemia

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