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

Study of sperm disomy in cases of male infertility with idiopathic severe oligoasthenoteratozoospermia

Male pseudohermaphroditismevaluation in Egyptian Children

Evaluation of psychosexual aspects of Egyptian infertile couples

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

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

Heme oxygenase -1 enzyme activity in semenand testicular tissue of azoospermic males

Role of cystic fibrosis transmembrane conductance regulator gene in azoospermic patients with congenital bilateral absence of the vas deferens in Egypt

Study of paraphilias and paraphilia-related disorders among outpatient males attending andrology and sexology department of Kasr El Eini hospital for sexual dysfunction

Seminal heme oxygenase in fertile and infertile males