Frontmatter

Articles in the same Issue

1. Frontmatter
2. Review
3. Prevalence of obesity and overweight in Iranian students: a systematic review and meta-analysis
4. Original Articles
5. Trends in pediatric obesity management, a survey from the Pediatric Endocrine Society Obesity Committee
6. Utility of MR proton density fat fraction and its correlation with ultrasonography and biochemical markers in nonalcoholic fatty liver disease in overweight adolescents
7. Vitamin D status and its relation to insulin resistance in a Mexican pediatric population
8. Elevated serum uric acid, hyperuricaemia and dietary patterns among adolescents in mainland China
9. Is there a relationship between the dietary inflammatory index and metabolic syndrome among adolescents?
10. New insights into the expression of androgen and estrogen receptors of the appendix testis in congenital cryptorchidism
11. General properties of autoimmune thyroid diseases and associated morbidities
12. Comparison of leptin levels in neonates born to mothers with high or low gestational weight gain
13. Percentile values of serum zinc concentration and prevalence of its deficiency in Iranian children and adolescents: the CASPIAN-V study
14. Nine-year overview of dyslipidemia management in children with heterozygous familial hypercholesterolemia: a university hospital outpatient lipid clinic project in Northwestern Greece
15. Gesell Developmental Schedules scores and the relevant factors in children with Down syndrome
16. Letters to the Editor
17. Society for Pediatric Radiology (SPR) Child Abuse Committee response regarding Miller, Stolfi and Ayoub’s flawed theories about child abuse and metabolic bone disease
18. Reply of Miller and Ayoub to Brown et al. Letter to the Editor
19. Case Reports
20. Identification of two novel variants in GAA underlying infantile-onset Pompe disease in two Pakistani families
21. Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route
22. Variant analysis of HPD genes from two families showing elevated tyrosine upon newborn screening by tandem mass spectrometry (MS/MS)
23. Challenges in the management of an ignored cause of hyperammonemic encephalopathy: pyruvate carboxylase deficiency
24. Autoimmune polyglandular syndrome type II with co-manifestation of Addison’s and Graves’ disease in a 15-year-old boy: case report and literature review