Masthead

Articles in the same Issue

1. Masthead
2. Masthead
3. Images in pediatric endocrinology
4. Leprechaunism (Donohue syndrome): report of a case in a newborn
5. Original articles
6. Children and adolescents with type 1 diabetes in Germany are more overweight than healthy controls: results comparing DPV database and CrescNet database
7. Age of onset of pubertal maturation of Thai boys
8. Plasma leptin and adiponectin concentrations correlate with cardiometabolic risk and systemic inflammation in healthy, non-obese children
9. Early differentiation between good and poor response to growth hormone therapy in short children born small for gestational age (SGA) to improve the outcome of poor responders
10. Children and adolescents with type 1 diabetes mellitus have a sixfold greater risk for prolonged QTc interval
11. Effect of micronutrient supplementation on height velocity of underprivileged girls in comparison with un-supplemented healthy controls
12. Insulin resistance in young adults born small for gestational age (SGA)
13. The effect of childhood obesity on cardiac functions
14. Adiponectin serum concentrations in newborn at delivery appear to be of fetal origin
15. Thalassaemic Osteopathy: a cross-sectional preliminary study from Sri Lanka
16. Health-related quality of life in Turner syndrome and the influence of key features
17. Clinical analysis on 33 patients with hypothalamic syndrome in Chinese children
18. The relationship between thyroid dose and diagnosis of primary hypothyroidism in pediatric brain tumor patients receiving craniospinal irradiation
19. Molecular characterization of Chilean patients with a clinical diagnosis of Noonan syndrome
20. Expensive therapies in children: benefit versus cost of combined treatment of recombinant human growth hormone and gonadotropin-releasing hormone analogue in girls with poor height potential
21. The absence of mutations in homeobox candidate genes HOXA3, HOXB3, HOXD3 and PITX2 in familial and sporadic thyroid hemiagenesis
22. A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism
23. Heterozygous GHR gene mutation in a child with idiopathic short stature
24. A novel compound mutation of CYP27B1 in a Chinese family with vitamin D-dependent rickets type 1A
25. A de novo mutation of DAX1 in a boy with congenital adrenal hypoplasia without hypogonadotropic hypogonadism
26. Patient reports
27. Hypercalcemia and osteolytic lesions as presenting symptoms of acute lymphoblastic leukemia in childhood. The use of zoledronic acid and review of the literature
28. Preterm ovarian hyperstimulation syndrome presented with vaginal bleeding: a case report
29. Pituitary stalk lesion in a 13-year-old female
30. Radiologic manifestation of a BCS1L-mutated patient
31. Permanent neonatal diabetes mellitus caused by a novel mutation in the KCNJ11 gene
32. NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients
33. A teenage boy with hypocalcemia after radioablation for Graves’ disease
34. Short communication
35. A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect
36. Letter to the Editor
37. Endometriosis and migraine: what is there behind the scenes?
38. 10.1515/jpem-2014-0999