Screening For Very Long Chain Fatty Acids in Egyptian Children with Inherited Peroxisomal Disorders

Preliminary Results of Neonatal Screening of 19 Genetic and Metabolic Disorders in Qalyubia Governorate

SELECTIVE SCREENING IN NEONATES SUSPECTED TO HAVE IEMS: A SINGLE CENTER STUDY IN UPPER EGYPT

Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study

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

Phenylketonuria in Sohag: A Preliminary Study

Inborn Errors of Metabolism among Suspected Patients Referred to the Genetic Clinic in Alexandria

Newborn Screening for Congenital Hypothyroidism and Congenital Adrenal Hyperplasia in Egypt

SIMPLE URINE METABOLIC SCRENING IN CHILDREN WITH REFRACTORY EPILEPSY IN ZAGAZIG UNIVERSITY CHILDREN'S

Evaluation of Metabolic Disorders in Pediatric Department at Zagazig University Hospital