Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia

Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia

DNA sequencing of uncharacterized β–globin gene mutations in β–thalassaemia in children

DNA sequencing of uncharacterized beta–globin gene mutations in beta–thalassaemia in children

In vitro stimulation of hemoglobin F production in thalassemic patients by the histone deacetylase inhibitor apicidin

The recent approach in management of thalassemia

The impact of iron regulating genes mutations on iron overload in β-thalassemia patients

New trends in mamagement of thalassemia in comparison with old conventional methodsof treatment

Effect of HFE gene (hemochromatosis in iron) mutation on iron overload in thalassemic patients

Oxidative stress and antioxidant status in β-thalassemia