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

Characterization of 42 Egyptian Children with Lysosomal Storage Disorders

Biochemical diagnosis of Wolman disease among patients with suspected lysosomal storage diseases

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

SCREENING OF EGYPTIAN PATEINTS SUFFERING FROM INBORN AMINO ACID METABOLIC DISORDERS

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

Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder

Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease

Some Hormonal and Biochemical Disorders in Patients of Down's syndrome in Egypt

Phenotypic Study of Egyptian Pediatric Patients with Criglar Najjar Syndrome