Hematological Findings in Nephropathic Cystinosis: Single Center Experience.

Outcome of Patients having Congenital Anomalies of the Kidney and Urinary Tract Associated with Congenital Heart Diseases in Pediatric Cardiac ICU.

Study of Genetic Variation in Podocin Gene Associated with Idiopathic Nephrotic Syndrome

Genetic Variations in the NPHS2 Gene in Children with Nephrotic Syndrome: A Cross-Sectional Study.

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

Congenital and Hereditary Renal Diseases in the Cairo Kidney Center: Review of the presenting Symptoms and Outcome –Any place for Screening?

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

Renal Cell Carcinoma: Recent Types and Challenges in Certain Tumor Typing

Molecular signaling pathways in an experimental model of Cardiorenal Syndrome

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