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

Pediatric Phenylketonuria in Fayoum Governorate (Retrospective study)

SCREENING OF EGYPTIAN PATEINTS SUFFERING FROM INBORN AMINO ACID METABOLIC DISORDERS

CLINICO-EPIDEMIOLOGICAL STUDY OF PHENYLKETONURIA IN INFANTS AND CHILDREN: A RETROSPECTIVE STUDY

The Effect of Phenylketonuria on the Quality of Life of the Affected children, Adolescents and their Parents at Minia Governorate.

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

Knowledge, Attitudes and Reported Practices for Mothers of Phenylketonuria Children at Hereditary Guideline Center in Assiut Governorate

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

Assessment of serum levels of zinc and copper in a sample of Egyptian children with phenylketonuria.

Hematological and biochemical parameters in various Clinical and Pharmacological types of Childhood Epilepsy