Nur Arslan

The prevalence of liver function abnormalities in pediatric celiac disease patients and its relation with intestinal biopsy findings.

Findings of hepatobiliary scintigraphy and liver biopsy in Maroteaux-Lamy syndrome presenting as neonatal cholestasis.

Hormones and cytokines in childhood obesity.

Mean platelet volume in obese adolescents with nonalcoholic fatty liver disease.

Evaluation of serum xenin and ghrelin levels and their relationship with nonalcoholic fatty liver disease and insulin resistance in obese adolescents.

Leptin-to-adiponectin ratio in obese adolescents with nonalcoholic fatty liver disease.

Aminotransferase elevations in rotavirus positive and negative acute gastroenteritis and its relation with disease severity.

Evaluation of the intraocular pressure in obese adolescents.

The effect of olive oil-based ketogenic diet on serum lipid levels in epileptic children.

Serum motilin levels and motilin gene polymorphisms in children with functional constipation.

Is ketogenic diet treatment hepatotoxic for children with intractable epilepsy?

The Effect of Ketogenic Diet on Serum Selenium Levels in Patients with Intractable Epilepsy.

Identification of three novel mutations in fourteen patients with citrullinemia type 1.

Analysis of hematological parameters in patients treated with ketogenic diet due to drug-resistant epilepsy.

Vitamin/mineral and micronutrient status in patients with classical phenylketonuria.

Elevated serum neopterin levels in children with functional constipation: association with systemic proinflammatory cytokines.

Effect of Ketogenic Diet on Motor Functions and Daily Living Activities of Children With Multidrug-Resistant Epilepsy: A Prospective Study.

Efficacy and tolerability of olive oil-based ketogenic diet in children with drug-resistant epilepsy: A single center experience from Turkey.

Robust, Long-Term Culture of Endoderm-Derived Hepatic Organoids for Disease Modeling.

Next-Generation Liver Medicine Using Organoid Models.

Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement.

Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients.

Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises.

Efficacy of Phenylalanine- and Tyrosine-Restricted Diet in Alkaptonuria Patients on Nitisinone Treatment: Case Series and Review of Literature.

High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.

Positive effects of ketogenic diet on weight control in children with obesity due to Prader-Willi syndrome.

Experience with cascade screening: A comprehensive family pedigree analysis of two index patients with Fabry disease.