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Cerebral hemodynamics and metabolism are similar in sickle cell disease patients with hemoglobin SS and Sβ 0 thalassemia phenotypes
Author(s) -
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.
Publication year - 2020
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.25698
Subject(s) - thalassemia , hemoglobinopathy , hemoglobin , medicine , phenotype , disease , hemodynamics , sickle cell anemia , hemoglobin s , metabolism , cardiology , genetics , biology , gene