Clinical, radiological and molecular studies of Egyptianchildren with achondroplasia

Molecular diagnosis of mitochondrial and nuclear DNA mutations among Egyptian children with mitochondrial encephalomyopathies

Congenital dyslipidemia among Egyptian children

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

Mucopolysaccharidosis in Egyptian children : Clinical and biochemical profile of 20 cases

Pulmonary hypertension in Egyptian sickle cell disease patients

The relation between right and left ventricular functions in pediatric dilated cardiomyopathy assessed by tissue Doppler : A study in pediatric dilated cardiomyopathy patients at Cairo University Pediatric Hospital

Allelic variation of angiotensin-converting enzyme gene in Egyptian children with nephrotic syndrome

Epidemiologic study of rheumatic cardiac affection in Egyptian children in the new millennium

Genetics of type 1 diabetes mellitus in Egyptian patients