AI Medical Compendium Journal:
Turk pediatri arsivi

Showing 1 to 4 of 4 articles

Single-pass albumin dialysis in a child aged six months with phenobarbital poisoning.

Turk pediatri arsivi
A girl aged six months was hospitalized because of resistant seizures and was discharged with phenobarbital and carbamazepine therapy. She was admitted to a state hospital with symptoms of inability to waken and difficulty in breathing. It was learne...

Assessment of different folic acid supplementation doses for low-birth-weight infants.

Turk pediatri arsivi
AIM: The adequacy of 50 mcg folic acid supplementation given to low-birth-weight babies was investigated. The folate levels of the mothers and infants, and breastmilk, and the optimum dose for folic acid supplementation were also investigated.

Clinical, molecular, and genetic evaluation of galactosemia in Turkish children.

Turk pediatri arsivi
AIM: Galactosemia is a carbohydrate metabolism disorder with autosomal recessive inheritance. The most frequent enzyme deficiency is galactose-1-phosphate-uridylytransferase, which causes classic galactosemia. When the enzyme is absent, an infant can...

Evaluation of macrophage activation syndrome associated with systemic juvenile idiopathic arthritis: single center experience over a one-year period.

Turk pediatri arsivi
AIM: This study aimed to evaluate the demographic, clinical, laboratory properties of patients with macrophage activation syndrome and treatment outcomes.