Masthead

Articles in the same Issue

1. Masthead
2. Masthead
3. Editorials
4. Editorial
5. Consensus, guidelines and reviews
6. Review article
7. Adaptation of glucose metabolism to fasting in young children with infectious diseases: a perspective
8. Images in pediatric endocrinology
9. Coexistence of testicular microlithiasis with parathyroid adenoma in an obese child
10. Original articles
11. Remission of hypertension and electrolyte abnormalities following renal transplantation in a patient with apparent mineralocorticoid excess well documented throughout childhood
12. Effects of metformin in children and adolescents with Prader-Willi syndrome and early-onset morbid obesity: a pilot study
13. Glycemic control in familial vs. sporadic type 1 diabetes patients over 5 years
14. Clinical and laboratory features of temporary brittle bone disease
15. Age of thelarche and menarche in contemporary US females: a cross-sectional analysis
16. Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism
17. Retinol and retinyl palmitate in fetal mice liver: sexual dimorphism
18. Skeletal maturation and predicted adult height in children with premature adrenarche
19. Homozygosity for a DTDST mutation in a child with multiple epiphyseal dysplasia
20. Body composition in young patients with galactose metabolic disorders: a preliminary report
21. Detection of vascular risk markers in children and adolescents with type 1 diabetes
22. X-linked recessive nephrogenic diabetes insipidus: a clinico-genetic study
23. Factors influencing neonatal thyroid-stimulating hormone concentrations as a measure of population iodine status
24. Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study
25. Patient reports
26. Hypothalamic hamartoma associated with central precocious puberty and growth hormone deficiency
27. A pediatric patient with Cushing syndrome caused by ectopic ACTH syndrome and concomitant pituitary incidentalomas
28. A novel genetic mutation in a Portuguese family with GCK-MODY
29. Permanent neonatal diabetes mellitus in monozygotic twins achieving low-dose sulfonylurea therapy
30. Hypocalcemia in a paediatric case: from the clinical features to diagnosis
31. A rare case of osteogenesis imperfecta combined with complete tooth loss
32. Iatrogenic acute pancreatitis due to hypercalcemia in a child with pseudohypoparathyroidism
33. Clinical expression of familial Williams-Beuren syndrome in a Turkish family
34. The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma
35. Low-level hyperinsulinism with hypoglycemic spells in an infant with mosaic Turner syndrome and mild Kabuki-like phenotype: a case report and review of the literature
36. Multiple cutaneous hemangiomas in a patient with combined pituitary hormone deficiency
37. Premature thelarche related to fennel tea consumption?
38. A novel insertion in the FOXL2 gene in a Chilean patient with blepharophimosis ptosis epicanthus inversus syndrome type I
39. Zellweger syndrome: prenatal and postnatal growth failure with epiphyseal stippling
40. Marine-Lenhart syndrome in a young girl
41. Novel AQP2 mutation causing congenital nephrogenic diabetes insipidus: challenges in management during infancy
42. Letter to the Editors
43. Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty
44. Carotid intima media thickness and echocardiography in risk stratification of obese adolescents with non-alcoholic fatty liver disease: what is the “right” approach?
45. Vitamin D and the heart: what is the truth?