Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/82542
Title: Dense cell formation in pediatric and adolescent patients with sickle cell disease
Authors: Abraham, E. C.
Bergherm, B.
Felice, Alex
McKie, Virgil C.
Abraham, A.
McKie, Kathleen M.
Keywords: Hemoglobin
Hemoglobinopathy
Sickle cell anemia
Molecular microbiology
Issue Date: 1986
Publisher: BMJ Group
Citation: Abraham, E. C., Bergherm, B., Felice, A., McKie, V., Abraham, A., & McKie, K. (1986). Dense cell formation in pediatric and adolescent patients with sickle cell disease. Clinical Research, 34(2), 449a.
Abstract: Previous studies on the influence of α-thalassemia (α-thal) on dense cell formation were done mostly in adult SS patients without much concern to discriminate the independent effect of age, Hb F levels, and α-thal. In this report we studied 15 SS patients with α-thal-2 heterozygosity (α-/αα) and 21 non-thalassemic (αα/αα) SS patients of age 2-13.
URI: https://www.um.edu.mt/library/oar/handle/123456789/82542
Appears in Collections:Scholarly Works - FacM&SSur

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