In patients with beta-thalassemia major, there was a highly significant linear increase in the percentages of blood OKT8(+) cells with an increasing number of units of erythrocytes transfused, irrespective of splenectomy [ 37 ].
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Total blood lymphocyte counts in hemochromatosis probands with HFE C282Y homozygosity: relationship to severity of iron overload and HLA-A and -B alleles and haplotypes.
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