Rev. Bras. Hematol. Hemoter. vol.25 número2

Similarly, no significant differences in the distributions of reticulocyte counts were found in the present study (Reference value: 1%; see Table S1,

and of the presence of α -thalassemia on clinical outcome and HbF expression may contribute to clarifying a possible relation- ship between clinical picture, ß S -haplotypes,

Analysis of oxidative status and biochemical parameters in adult patients with sickle cell anemia treated with hydroxyurea, Ceará-Brazil. Rev Bras

In the absence of a national record of sickle cell disease in Brazil, contributions like the article “Demographic aspects and quality of life of patients with sickle cell anemia” are

Tumor necrosis factor-alpha levels were lower in sickle cell anemia patients who were receiving hydroxyurea treatment than those who were not (p-value = 0.1249).. Sickle cell

Evaluation of red cell and reticulocyte parameters as indicative of iron deficiency in patients with anemia of chronic disease. Rev Bras

The thematic units were: identification of the pain of the child with sickle cell disease by the nurse; strategies to evaluate and control the pain of the child; and impact of

This is a cross-sectional study carried out between November 2007 and January 2009 in children with Sickle Cell Anemia and Hemoglobin SC disease, regularly monitored at a NSRS in