Diagnosis and follow-up of patients with phenylketonuria

Identificaton and treatment of inbornerrors of metabolism causingintractable infantile seizures

Detection of inborn errors of metabolism among pediatric patients admitted to pediatric ICU

Diagnosis of nonatal seizures of inherited metabolic origin

Follow-up of treated nephropathic cystinosis children

Assessment of adjustment pattern of children suffering from phenylketonuria

Congenital adrenal hyperplasia due to11 β hydroxylase deficiency : A clinical and diagnostic approach

Metabolic liver diseases in infancy and childhood : Update in diagnosis and management

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

Etiology of congenital hypothyroidism revealed by newborn screening