Screening of inborn errors of metabolism among Egyptian pediatric intensive care unit (PICU) patients by tandem mass spectrometry

Organic aciduria in Egyptianinfants and children

A pilot study for the prevalence of methylenetetrahydrofolate reductase gene mutation in Egyptian children with homocystinuria

Clinical biochemical markers for hepatocellular carcinoma in Egyptian patients

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

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

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

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

Molecular study and carrier detection of alpha thalassaemia in egypt

Validation of triple marker medians used in antenatal screening of Egyptian Females