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Publisher's Note

Published/Copyright: June 13, 2011
Journal of Pediatric Endocrinology and Metabolism
From the journal Volume 24 Issue 5-6

Published Online: 2011-06-13
Published in Print: 2011-06-01

©2011 by Walter de Gruyter Berlin Boston

Articles in the same Issue

  1. Publisher's Note
  2. Publisher's Note
  3. Editorial
  4. The damage caused by incomplete and uncontrolled medical information
  5. Images in Pediatric Endocrinology
  6. Dorsolumbar kyphosis: diagnostic value of hook shaped vertebra
  7. Original Contributions
  8. Are adolescent weight-related problems and general well-being essentially an issue of age, gender or rather a pubertal timing issue?
  9. Comparison of methimazole and propylthiouracil in the management of children and adolescents with Graves’ disease: efficacy and adverse reactions during initial treatment and long-term outcome
  10. The effect of glucocorticoid replacement therapy on bone mineral density in children with congenital adrenal hyperplasia
  11. Treatment of symptomatic osteoporosis in children: a comparison of two pamidronate dosage regimens
  12. Stanozolol regulates proliferation of growth plate chondrocytes via activation of ERα in GnRHa-treated adolescent rats
  13. A case of McCune-Albright syndrome associated with pituitary GH adenoma: therapeutic process and autopsy
  14. The role of metabolic syndrome components and adipokines in insulin resistance in prepubertal children
  15. A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones
  16. Causes and patterns of referral to a tertiary, multidisciplinary program for the treatment of childhood obesity
  17. Vitamin D receptor genotypes are associated with bone mass in patients with Turner syndrome
  18. Plasma leptin and adiponectin concentrations in healthy, non-obese children
  19. Puberty and pubertal growth dynamics in children with idiopathic short stature
  20. Endocrine complications following pediatric bone marrow transplantation
  21. Rare hypertension as a result of 17α-hydroxylase deficiency
  22. Girls with early puberty attain a near-final height similar to their target height
  23. Persistent hyperthyrotropinemia in congenital hypothyroidism: successful combination treatment with levothyroxine and liothyronine
  24. Benign transient hyperphosphatasemia in infants and children: a prospective cohort
  25. The relation between 25-hydroxyvitamin D with peak bone mineral density and body composition in healthy young adults
  26. Childhood obesity: evidence of an association between plasminogen activator inhibitor-1 levels and visceral adiposity
  27. Glargine basal-bolus insulin regimen versus insulin pump therapy: comparison of glycemic control
  28. Patient Report Letters
  29. A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitus
  30. HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes
  31. A newborn case with perinatal-lethal Gaucher disease due to R463H homozygosity complicated by C677T homozygosity in the MTHFR gene
  32. Hyperthyroidism presenting with hyperglycemia in an adolescent female
  33. Short Communications
  34. A single base-pair deletion in the WFS1 gene causes Wolfram syndrome
  35. Growth suppression caused by corticosteroid eye drops
  36. Familial glucocorticoid deficiency due to compound heterozygosity of two novel MC2R mutations
  37. Letter to the Editor
  38. Meetings
  39. Meetings Calendar
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