A biochemical study of glycogen storage disease in Egyptian children : The value of assessing fasting tolerance

Metachromatic leukodystrophy in Egyptianchildren with dysmyelinating brain disease

Organic aciduria in Egyptianinfants and children

Plasma chitotriosidase enzyme activity in Egyptian patients with nephropathic cystinosis

A clinical and molecular genetic study on Egyptian children with hypertrophic cardiomyopathy

Nephrotic syndrome in Egyptiachildren : A single centre experience

Clinical, radiological and molecular studies of Egyptianchildren with achondroplasia

Clinical phenotypes of renal cystic diseases in Egyptian children

Cholestatic disorders of infancy : A descriptive study in the Pediatric Hepatology Unit at Cairo University Children's Hospital

Congenital dyslipidemia among Egyptian children