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

Ciliopathies and Renal Diseases

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

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.

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

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

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

Pattern of Renal Diseases Among Children Admitted to Assiut University Children Hospital.