Frontmatter

Articles in the same Issue

1. Frontmatter
2. Original Articles
3. Vitamin D status in Israeli pediatric type 1 diabetes patients: the AWeSoMe Study Group experience and literature review
4. Metabolic features and changes in glucose-induced serum glucagon-like peptide-1 levels in children with hypothalamic obesity
5. Assessment of intima-media thickness of the carotid artery and intraluminal diameter of the brachial artery as cardiovascular risk markers in Brazilian adolescents with overweight or obesity
6. The role of LCPUFA-ω3 on the obesity-associated hyperandrogenemia of pubertal girls: secondary analysis of a randomized clinical trial
7. Genetic variants of the phenylalanine hydroxylase gene in patients with phenylketonuria in the northeast of Iran
8. Oral health status of children with phenylketonuria
9. Birth weight related blood concentrations of the neurotransmission amino acids glutamine plus glutamate, phenylalanine and tyrosine in full-term breastfed infants perinatally
10. Hyperthyrotropinemia is common in preterm infants who are born small for gestational age
11. Radioactive iodine therapy for pediatric Graves’ disease: a single-center experience over a 10-year period
12. The decision-making levels of urine tetrasaccharide for the diagnosis of Pompe disease in the Turkish population
13. A questionnaire study on sleep disturbances associated with Prader-Willi syndrome
14. Body size measurements, digit ratio (2D:4D) and oestrogen and progesterone receptors’ expressions in juvenile gigantomastia
15. The effect of celiac disease and gluten-free diet on pubertal development: a two-center study
16. Observational study of disorders of sex development in Yaounde, Cameroon
17. Letter to the Editor
18. Reforming the male Tanner genital scale
19. Short Communication
20. The association between vitamin D levels and precocious puberty: a meta-analysis
21. Case Reports
22. Partial trisomy 9p and 14q microduplication in a patient with growth retardation: a case report and review of the literature
23. Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation
24. Patient report
25. Marked phenotypic variable expression among brothers with duplication of Xq27.1 involving the SOX3 gene
26. Case Report
27. Does the risk of arterial hypertension increase in the course of triptorelin treatment?