Needle detachment from the Sure-T® infusion set in two young children with diabetes mellitus (DM) treated with continuous subcutaneous insulin infusion (CSII) and unexplained hyperglycaemia

Artikel in diesem Heft

1. Frontmatter
2. Highlight: Childhood Craniopharyngioma
3. Selected papers from the 3rd International Multidisciplinary Postgraduate Course, April 24–27, 2014
4. Childhood craniopharyngioma – current status and recent perspectives in diagnostics and treatment
5. The importance of interdisciplinary communication with patients about complex, chronic illnesses: our experiences as parents of a child with a craniopharyngioma
6. Adamantinomatous craniopharyngioma: pathology, molecular genetics and mouse models
7. Endocrine aspects and sequel in patients with craniopharyngioma
8. Surgery for pediatric craniopharyngiomas: is less more?
9. Eating behavior, weight problems and eating disorders in 101 long-term survivors of childhood-onset craniopharyngioma
10. Carbohydrate-lipid profile and use of metformin with micronized fenofibrate in reducing metabolic consequences of craniopharyngioma treatment in children: single institution experience
11. Effects of T3 treatment on brown adipose tissue and energy expenditure in a patient with craniopharyngioma and hypothalamic obesity
12. Hypothalamic obesity after treatment for craniopharyngioma: the importance of the home environment
13. Review article
14. Association study of TAC3 and TACR3 gene polymorphisms with idiopathic precocious puberty in Chinese girls
15. Images in pediatric endocrinology
16. Intestinal invagination in diabetic ketoacidosis: case report
17. Original articles
18. Managing incidental findings and disclosure of results in a paediatric research cohort – the LIFE Child Study cohort
19. The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation
20. Gender differences and age-related changes in body fat mass in Tibetan children and teenagers: an analysis by the bioelectrical impedance method
21. A study of genes involved in adipocyte differentiation
22. Initiation of growth hormone therapy in idiopathic short stature: do gender differences exist?
23. The influence of puberty on vitamin D status in obese children and the possible relation between vitamin D deficiency and insulin resistance
24. Growth failure associated with early neglect: pilot comparison of neglected US children and international adoptees
25. Effect of growth hormone deficiency on brain MRI findings among children with growth restrictions
26. Variability of lipid and lipoprotein concentrations during puberty in Brazilian boys
27. Skin advanced glycation endproducts are elevated at onset of type 1 diabetes in youth
28. Can optical coherence tomography predict early retinal microvascular pathology in type 1 diabetic adolescents without minimal diabetic retinopathy? A single-centre study
29. Decreased levels of homoarginine and asymmetric dimethylarginine in children with type 1 diabetes: associations with cardiovascular risk factors but no effect by atorvastin
30. Influence of catch-up growth on abdominal fat distribution in very low birth weight children – cohort study
31. Thyrotoxic, hypokalemic periodic paralysis (THPP) in adolescents
32. Pulmonary function in children with type 1 diabetes mellitus
33. Identification of deletions in children with congenital hypothyroidism and thyroid dysgenesis with the use of multiplex ligation-dependent probe amplification
34. Effect of l-thyroxine supplementation on infants with transient hypothyroxinemia of prematurity at 18 months of corrected age: randomized clinical trial
35. Vitamin D-containing supplements for children between 1–3 years of age: Are they essential for bone health?
36. Anti-Mullerian hormone levels in American girls by age and race/ethnicity
37. The effect of tailoring of cornstarch intake on stature in children with glycogen storage disease type III
38. Thyroid disease in Chinese girls with Turner syndrome
39. Patient reports
40. Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report
41. Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX gene
42. Novel heterozygous IGF1R mutation in two brothers with developing impaired glucose tolerance
43. A case of pediatric ectopic thyroid in lateral lymph nodes
44. Hyperostosis-hyperphosphatemia syndrome (HHS): report of two cases with a recurrent mutation and review of the literature
45. Needle detachment from the Sure-T® infusion set in two young children with diabetes mellitus (DM) treated with continuous subcutaneous insulin infusion (CSII) and unexplained hyperglycaemia
46. Familial dysalbuminemic hyperthyroxinemia in a 4-year-old girl with hyperactivity, palpitations and advanced dental age: how gold standard assays may be misleading