Variants of precocious puberty in Egypt

Epidemiology and clinical characters of congenital adrenal hyperplasia patientsattending endocrinology Clinic at CairoUniversity Children’s Hospital

Mutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia

Molecular characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children

Disorders of sex development as a part of developmental syndromes

Gonadal function in adult Egyptian thalassemic patients

Clinical and genetic study of 46 XY DSD due to androgen receptor defect due to defect in the gene on Xq13

Congenital adrenal hyperplasia due to11 β hydroxylase deficiency : A clinical and diagnostic approach

Clinical phenotypes of renal cystic diseases in Egyptian children

Nephrotic syndrome in Egyptiachildren : A single centre experience