Detection of inborn errors of metabolism among pediatric patients admitted to pediatric ICU

Pilot study for Egyptian age related reference values for amino acid and acylcarnitines by tandem mass spectrometry

Organic aciduria in Egyptianinfants and children

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

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

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

Genetic screening for alpha thalassemia mutations among Egyptian neonates

Screening and management of different grades ofpulmonary hypertension in Neonatal IntensiveCare Unit of Cairo University Pediatric Hospital

SCREENING OF EGYPTIAN PATEINTS SUFFERING FROM INBORN AMINO ACID METABOLIC DISORDERS

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