background: many efforts have been undertaken until now to find an alternative approach to packed red cell tranfusion in major β-thalassemia. augmentation of fetal hemoglobin by hydroxyurea has proved to be less effective in this condition as compared to sickle cell anemia, probably due to molecular heterogeneity of the former disease. hydroxyurea efficacy and its relation to xmn1 polymorphism ...

our previous studies on thalassemia patients, homozygous or compound heterozygous for severe beta thalassemia mutations, has suggested that 5’hs4-lcr and/or xmn1-hbg2 backgrounds, which were linked in our thalassemia patients, are important in determining the blood transfusion dependency of these individuals. while the majority of patients with aa/-- 5’hs4/xmn1 background, were severely depende...

Influence of the magnetoelastic interaction on the structural phase transitions in cubic ferromagnets is investigated on the basis of a Ginzburg-Landau theory. It is shown that for the case of a positive magnetic anisotropy constant the structural phase transitions are not accompanied by a spin-reorientation. In the magnetic state the high-temperature phase has small deformations caused by the ...