Pulmonary hypertension in Egyptian sickle cell disease patients

Association between XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patient

Phenotypic variability of Egyptian children with thalassemia intermedia and treatment response

Oxidative status among Egyptian children with sickle cell anemia

Studyy of some of the ameliorating factors in homozygous Beta thalassemia

A study of renal findings in pediatric Beta-thalassemia in Egyptian patients

A study of the prevalence and risk factors of hepatobiliary dysfunction in Egyptian children with chronic hemolytic anemia

Study of autoimmune hemolytic anemia in Egyptian children

Genetic screening for alpha thalassemia mutations among Egyptian neonates

Study of serum hepcidin as a diagnostic tool of iron overload in Egyptian children with beta-thalassemia major and intermedia