Received: 2011-12-25
Accepted: 2012-1-4
Published Online: 2012-02-20
Published in Print: 2012-04-01
©2012 by Walter de Gruyter Berlin Boston
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Artikel in diesem Heft
- Review Articles
- Peptide YY in children: a review
- Brown adipose tissue: distribution and influencing factors on FDG PET/CT scan
- Mini Review
- Approach to the management of slipped capital femoral epiphysis and primary hyperparathyroidism
- Original Articles
- Current normal values for TSH and FT3 in children are too low: evidence from over 11,000 samples
- Elevated serum ferritin and soluble transferrin receptor in infants with congenital hypothyroidism
- Implications of gastrointestinal hormones in the pathogenesis of obesity in prepubertal children
- Oxidative stress in obese children and its relation with insulin resistance
- Final height in elite male artistic gymnasts
- Expression of SOCS1, SOCS2, and SOCS3 in growth hormone-stimulated skin fibroblasts from children with idiopathic short stature
- Evaluation of skeletal maturity score for Korean children and the standard for comparison of bone age and chronological age in normal children
- Children and adolescent acceptability of a new device system to administer human growth hormone – a pilot study
- The analysis of clinical manifestations and genetic mutations in Chinese boys with primary adrenal insufficiency
- Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns
- Prevention of bone loss in children receiving long-term glucocorticoids with calcium and alfacalcidol or menatetrenone
- Evaluation of serum kisspeptin levels in girls in the diagnosis of central precocious puberty and in the assessment of pubertal suppression
- Hypophosphatemia in small for gestational age extremely low birth weight infants receiving parenteral nutrition in the first week after birth
- Patient Reports
- Partial benefit of anastrozole in the long-term treatment of precocious puberty in McCune-Albright syndrome
- Palmoplantar keratoderma with growth hormone deficiency
- Propylthiouracil hepatitis: report of a case and extensive review of the literature
- Autonomous functioning thyroid nodule successfully treated with radioiodine in a 3 and a half-year-old boy
- Hashimoto thyroiditis associated with ataxia telangiectasia
- Improved long-term glucose control in neonatal diabetes mellitus after early sulfonylurea allergy
- Stroke in a child with Adams-Oliver syndrome and mixed diabetic ketoacidosis and hyperglycemic hyperosmolar syndrome
- A novel mutation of the insulin receptor gene in a preterm infant with Donohue syndrome and heart failure
- Permanent neonatal diabetes mellitus due to KCNJ11 mutation in a Portuguese family: transition from insulin to oral sulfonylureas
- Successful prospective management of neonatal citrullinemia
- A Chinese patient with acquired partial lipodystrophy caused by a novel mutation with LMNB2 gene
- Warburg Micro syndrome
- Inguinal ovary as a rare diagnostic sign of Mayer-Rokitansky-Küster-Hauser syndrome
- Letters to the Editor
- Endocrine disruptors and fulminant type 1 diabetes: is there a link?
- The appropriate use of sensitive tests of hypothalamic-pituitary-adrenal-axis suppression
- Meetings
- Meetings Calendar
- Masthead
- Masthead
Schlagwörter für diesen Artikel
cosyntropin test;
hypothalamic pituitary adrenal axis;
metyrapone test
Artikel in diesem Heft
- Review Articles
- Peptide YY in children: a review
- Brown adipose tissue: distribution and influencing factors on FDG PET/CT scan
- Mini Review
- Approach to the management of slipped capital femoral epiphysis and primary hyperparathyroidism
- Original Articles
- Current normal values for TSH and FT3 in children are too low: evidence from over 11,000 samples
- Elevated serum ferritin and soluble transferrin receptor in infants with congenital hypothyroidism
- Implications of gastrointestinal hormones in the pathogenesis of obesity in prepubertal children
- Oxidative stress in obese children and its relation with insulin resistance
- Final height in elite male artistic gymnasts
- Expression of SOCS1, SOCS2, and SOCS3 in growth hormone-stimulated skin fibroblasts from children with idiopathic short stature
- Evaluation of skeletal maturity score for Korean children and the standard for comparison of bone age and chronological age in normal children
- Children and adolescent acceptability of a new device system to administer human growth hormone – a pilot study
- The analysis of clinical manifestations and genetic mutations in Chinese boys with primary adrenal insufficiency
- Replication of clinical associations with 17-hydroxyprogesterone in preterm newborns
- Prevention of bone loss in children receiving long-term glucocorticoids with calcium and alfacalcidol or menatetrenone
- Evaluation of serum kisspeptin levels in girls in the diagnosis of central precocious puberty and in the assessment of pubertal suppression
- Hypophosphatemia in small for gestational age extremely low birth weight infants receiving parenteral nutrition in the first week after birth
- Patient Reports
- Partial benefit of anastrozole in the long-term treatment of precocious puberty in McCune-Albright syndrome
- Palmoplantar keratoderma with growth hormone deficiency
- Propylthiouracil hepatitis: report of a case and extensive review of the literature
- Autonomous functioning thyroid nodule successfully treated with radioiodine in a 3 and a half-year-old boy
- Hashimoto thyroiditis associated with ataxia telangiectasia
- Improved long-term glucose control in neonatal diabetes mellitus after early sulfonylurea allergy
- Stroke in a child with Adams-Oliver syndrome and mixed diabetic ketoacidosis and hyperglycemic hyperosmolar syndrome
- A novel mutation of the insulin receptor gene in a preterm infant with Donohue syndrome and heart failure
- Permanent neonatal diabetes mellitus due to KCNJ11 mutation in a Portuguese family: transition from insulin to oral sulfonylureas
- Successful prospective management of neonatal citrullinemia
- A Chinese patient with acquired partial lipodystrophy caused by a novel mutation with LMNB2 gene
- Warburg Micro syndrome
- Inguinal ovary as a rare diagnostic sign of Mayer-Rokitansky-Küster-Hauser syndrome
- Letters to the Editor
- Endocrine disruptors and fulminant type 1 diabetes: is there a link?
- The appropriate use of sensitive tests of hypothalamic-pituitary-adrenal-axis suppression
- Meetings
- Meetings Calendar
- Masthead
- Masthead