Biochemical Diagnosis of Peroxisomal Disorders by GC/MS: Egyptian Patients with X-linked Adrenoleukodystrophy

SCREENING OF EGYPTIAN PATEINTS SUFFERING FROM INBORN AMINO ACID METABOLIC 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

Phenylketonuria in Sohag: A Preliminary Study

Evaluation of Metabolic Disorders in Pediatric Department at Zagazig University Hospital

Screening the Egyptian Children with Metabolic Disorders Using the Modified Checklist of Autism

Newborn Screening for Congenital Hypothyroidism and Congenital Adrenal Hyperplasia in Egypt

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

Screening of Metabolic Syndrome in Children and Adolescents in Benha City, Egypt