STUDY OF CLINICAL AND PROTHROMBOTIC GENE MUTATION AS PREDICTORS OF THROMBOEMBOLISM IN PEDIATRIC CANCER

Assessment of factor V leiden, prothrombin gene mutation and methylenetetrahydrofolate reductase activity in pediatric patients with thalassemia

HEMOCHROMATOSIS HFE GENE POLYMORPHISM AND DEVELOPMENT OF PREDIABETES AND DIABETES MELLITUS IN B THALASSEMIC PATIENTS

Relationship between polymorphisms in thrombophilic genes and preeclampsia In Egyptian population

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

The Risk of Development of Thrombocytopenia during Valproic Acid Therapy in Children Attending Aswan University Hospitals

Association of Protein Z intronic G79A Polymorphism with susceptibility to deep vein thrombosis in Egyptian patients with Behcet's disease: A preliminary report

PROTHROMBIN GENE G20210A MUTATION IN PATIENTS WITH ACUTE DEEP VENOUS THROMBOSIS

Association of factor V leiden and prothrombin gene mutations with thrombotic risk in patients with sickle cell anemia

Prothrombin G20210A Mutation in Women with Preeclampsia in Alexandria