A Genetic Risk Factor in Egyptian Children with A Family History of End-Stage Renal Disease

Plausibility of the Application of SNPs Haplotype Analysis within the Renalase Gene in Children with a Family History of Chronic Kidney Disease.

Serum Fibroblast Growth Factor 23 as an Early Biomarker for Detection of Renal Osteodystrophy and Progression of Chronic Kidney Disease in Children

Relation between Endothelial Protein C Receptor Gene Polymorphism 6936A/G and the Risk of Vascular Access Thrombosis in Patients with End Stage Renal Disease on Hemodialysis

Soluble Alpha Klotho Serum Level in Chronic Kidney Disease

Evaluation of NPHS2 gene polymorphism (R229Q) in chronic kidney disease patients

Association Study of Vitamin D Deficiency and its receptor Gene Polymorphism in Diabetic Nephropathy Progression

CHEMOKINE RECEPTOR 2 (CCR2) G190A POLYMORPHISM IN CHRONIC RENAL FAILURE PATIENTS REQUIRING HEMODIALYSIS

Clinical, Biochemical, and Genetic Study of Patients with Hypertension Associated Kidney Disease

Fibroblast Growth Factor 23 and Carotid Artery Intima Media Thickness in Children with Chronic Kidney Disease