Growth hormone mortality: will history repeat itself?

Articles in the same Issue

1. Masthead
2. Masthead
3. Editorial
4. Growth hormone mortality: will history repeat itself?
5. Review articles
6. Interval training and the GH-IGF-I axis – a new look into an old training regimen
7. Bone health in children and adolescent with Turner syndrome
8. Metabolic alterations in pregnant women: gestational diabetes
9. Short communication
10. A method to determine the likelihood of transition to puberty in a heterogeneous prepubertal age group
11. Images in pediatric endocrinology
12. Hypopituitarism occurring in neonatal sepsis
13. Original articles
14. In congenital hypothyroidism, an initial L-thyroxine dose of 10–12 μg/kg/day is sufficient and sometimes excessive based on thyroid tests 1 month later
15. TSH suppression after intravenous glucocorticosteroid administration in preterm infants
16. Frequency of subclinical hypothyroidism in 5- to 15-year-old children with migraine headache
17. Higher dose of methimazole causes frequent adverse effects in the management of Graves’ disease in children and adolescents
18. Water deprivation test in children with polyuria
19. Training increases anabolic response and reduces inflammatory response to a single practice in elite male adolescent volleyball players
20. Positive effects of zinc supplementation on growth, GH, IGF1, and IGFBP3 in eutrophic children
21. A novel intronic mutation in SHOX causes short stature by disrupting a splice acceptor site: direct demonstration of aberrant splicing by expression of a minigene in HEK-293T cells
22. Increased growth hormone receptor (GHR) degradation due to over-expression of cytokine inducible SH2 domain-containing protein (CIS) as a cause of GH transduction defect (GHTD)
23. Japanese growth prediction model for prepubertal children with growth hormone deficiency
24. Clinical features and management of diabetic ketoacidosis in different age groups of children: children less than 5 years of age are at higher risk of metabolic decompensation
25. Relationship between left ventricular mass and carotid intima media thickness in obese adolescents with non-alcoholic fatty liver disease
26. Serum ischemia-modified albumin level and its association with cardiovascular risk factors in obese children and adolescents
27. Obesity, insulin resistance, and the risk of an elevated alanine aminotransferase activity in the Korean adolescent population
28. Leptin and IGF-I/II during the first weeks of life determine body composition at 2 years in infants born with very low birth weight
29. Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele
30. Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia
31. Low bone status in Indian growth hormone-deficient children
32. Gender related differences in glucocorticoid therapy and growth outcomes among pubertal children with 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH)
33. Elevated serum anti-Müllerian hormone in adolescents with polycystic ovary syndrome: relationship to ultrasound features
34. Recurrent hypoglycemia due to growth hormone deficiency in an infant with Turner syndrome
35. Patient reports
36. Intrathyroidal ectopic thymic tissue may mimic thyroid cancer: a case report
37. Hypercortisolism and hypothyroidism in an infant with Smith-Lemli-Opitz syndrome
38. Peripheral precocious puberty due to inadvertent exposure to testosterone: case report and review of the literature
39. Absent phallus: issues in management
40. A case of recurrent labial adhesions in a 15-month-old child with asymptomatic non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
41. Response to growth hormone treatment in a patient with 18p-syndrome
42. Hypodipsic hypernatremia leading to reversible renal failure following surgery for craniopharyngioma
43. Transient isolated marked elevation of midregion parathyroid hormone fragments in an infant
44. A novel splice site mutation of the beta subunit gene of epithelial sodium channel (ENaC) in one Turkish patient with a systemic form of pseudohypoaldosteronism type 1
45. Letters to the editor
46. What is the priority in nutritional rickets: prevention or therapy?
47. The true relation between vitamin D and insulin sensitivity: is it easy to establish?
48. Birth asphyxia and hypothermia therapy: is survivin the orchestrator of recovery?
49. Delayed cord clamping in intrauterine growth restriction (IUGR) neonates: is there a need to establish clinical cut-off score for inclusion?