Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/82332
Title: Hemorheologic parameters in children with homozygous Sickle Cell Anemia receiving chronic red cell transfusions for large cerebral vessel vasculopathy (LCVV)
Authors: Sabio, H.
McKie, Virgil C.
McKie, Kathleen M.
Jeraldo, T. L.
Adams, R. A.
Felice, Alex
Keywords: Hemoglobin
Hemoglobinopathy
Sickle cell anemia
Molecular microbiology
Issue Date: 1988
Citation: Sabio, H., McKie, V., McKie, K. M., Jeraldo, T. L., Adams, R. A., & Felice, A. (1988). Hemorheologic parameters in children with homozygous Sickle Cell Anemia receiving chronic red cell transfusions for large cerebral vessel vasculopathy (LCVV). National Sickle Cell Meeting, Washington, DC.
Abstract: Five children with homozygous sickle cell anemia (SCA) !Without associated alpha thalassemia receiving partial exchange transfusions designed to maintain the % Hb S between 30-15 for 3 management of LCVV were studied.
URI: https://www.um.edu.mt/library/oar/handle/123456789/82332
Appears in Collections:Scholarly Works - FacM&SSur



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