Glucose-6-phosphate dehydrogenase deficiency among newborns with indirect hyperbilirubinaemia

Gene mutation and qualitative enzyme assay of G6PD enzyme deficiency in neonatal hyperbilirubinemia

Screening for betathalassemia in Damietta

Genetic screening for alpha thalassemia mutations among Egyptian neonates

Assessment of the efficacy of haptoglobin as a detector for neonatal jaundice

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

Identification of the neutrophil phagocytic function in cord blood of neonates with variable gestational ages

Genotype and phenotype correlation in glucose-6- phosphate dehydrogenase deficiency

Etiology of congenital hypothyroidism revealed by newborn screening

Complete blood count in the neonatal intensive care unit