A rare case of isolated Cushing syndrome in a 3-month-old boy

Artikel in diesem Heft

1. Masthead
2. Masthead
3. Editorial
4. Success has many fathers, failure is orphan
5. Review Article
6. Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges
7. Original Articles
8. Temporary brittle bone disease: association with intracranial bleeding
9. Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I
10. Application of liquid chromatography-tandem mass spectrometry in the diagnosis and follow-up of maple syrup urine disease in a Chinese population
11. The role of uncoupling protein 2 and 3 genes polymorphism and energy expenditure in obese Indonesian children
12. Thyroid dysfunctions of prematurity and their impacts on neurodevelopmental outcome¹⁾
13. Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period
14. Reference intervals for serum thyroid hormones in preterm hospitalized infants¹⁾
15. The clinical and biochemical presentation of vitamin D deficiency and insufficiency in children and adolescents
16. A risk score for identifying overweight adolescents with dysglycemia in primary care settings¹⁾
17. Thyroid function and morphology in overweight and obese children and adolescents in a Chinese population
18. Propionic acidaemia: demographic characteristics and complications^a
19. Negative correlation between serum IL-6 level and cardiorespiratory fitness in 10- to 11-year-old boys with increased BMI
20. Penile length and genital anomalies in Egyptian male newborns: epidemiology and influence of endocrine disruptors
21. Efficacy of vitamin D loading doses on serum 25-hydroxy vitamin D levels in school going adolescents: an open label non-randomized prospective trial
22. Characteristics of infants admitted with hypoglycemia to a neonatal unit
23. Increasing thyroid-stimulating hormone is associated with impaired glucose metabolism in euthyroid obese children and adolescents
24. The role of FTO genotype on eating behavior in obese Sardinian children and adolescents
25. Prevalence of multiple forms of autoimmunity in Egyptian patients with Turner syndrome: relation to karyotype
26. A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree
27. Patient Reports
28. Pseudohypoparathyroidism type Ia: a novel GNAS mutation in a Brazilian boy presenting with an early primary hypothyroidism
29. Diabetic ketoacidosis with cerebral hemorrhage and alpha coma in an adolescent female
30. A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism
31. Citric acid as the last therapeutic approach in an acute life-threatening metabolic decompensation of propionic acidaemia
32. A case of autosomal dominant osteopetrosis type II with a novel TCIRG1 gene mutation
33. The interpretation of color – an endocrine cause of skin discoloration mimicking cyanosis
34. Novel heterozygous thyrotropin receptor mutation presenting with neonatal hyperthyrotropinaemia, mild thyroid hypoplasia and absent uptake on radioisotope scan
35. Turner Syndrome and apparent absent uterus: a case report and review of the literature
36. 10.1515/jpem-2012-0133
37. Vaginal bleeding in a 4-month-old preterm girl: extreme minipuberty mimicking central precocious puberty
38. A rare case of isolated Cushing syndrome in a 3-month-old boy
39. Letters to the Editors
40. Gynecomastia in puberty is usually asymptomatic and regresses spontaneously
41. Is endometriosis ultimately the end result of the interplay between interferon-γ (IFN-γ) and the HOXA10 gene network?
42. Does treatment with L-selenomethionine reduce thyroid volume in euthyroid children with autoimmune thyroiditis?
43. Meetings
44. Meetings Calendar