Inclusion bodies in the red cells of pahemichrome. In the present study, mitients with thalassemia syndromes may crospectrophotometric examination of result from precipitation of those single inclusion bodies in ghosts prehemoglobin subunits that are produced pared from the red cells of two patients in relative excess. In hemoglobin H diwith fl-thalassemia major revealed the sease, a form of a-...

hemoglobin f (hbf, α 2 γ 2 ) is a major contributor to the clinical heterogeneity and ameliorating agent observed in patients with the β-globin disorders including β-thalassemia and sickle cell disease (scd). during fetal life, hbf is the major hemoglobin but is largely substituted by adult hemoglobin (hba, α 2 β 2 ) following a globin expression switch after birth. increased γ-globin expressio...

patients and methods in this cross-sectional study, the hemoglobin levels of 52 patients with end-stage renal disease were measured before and after hemodialysis. the required erythropoietin doses and the differences in cost were calculated based on the hemoglobin levels before and after hemodialysis. a model to predict the adjusted erythropoietin dosages based on post-hemodialysis hemoglobin l...