Molecular diagnosis of mitochondrial and nuclear DNA mutations among Egyptian children with mitochondrial encephalomyopathies

Methyl tetrahydrofolate reductase C677T gene mutation as a risk factor for diabetic nephropathy in type 2 diabetes

Association study of uncouplingprotein2 polymorphism with myeloperoxidase in diabetic patients type 2

Metallothionein polymorphism as a risk factor for cardiovascular complications in type 2 diabetic patients

Study of platelet and endothelial microparticles in patients with type 2 diabetes mellitus

Trace element levels and malondialdehyde in non-insulin dependent diabetes mellitus

Paraoxonase gene polymorphism as a marker for early microvascular complications in type 1 diabetes mellitus

Study of mutation in NAD (P) H : Quinone oxidoreductase 1 alleles in patients with acute leukemia

Pilot study of insulin resistance in type 2 diabetes mellitus

Molecular genetics in type 2 diabetes mellitus