Published Online: 2011-10-1
Published in Print: 2011-10-1
©2011 by Walter de Gruyter Berlin Boston
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Artikel in diesem Heft
- Editorial
- IGF-I in extremely low birth weight (ELBW): a long-term observation
- Original Articles
- A potential role for adjunctive vitamin D therapy in the management of weight gain and metabolic side effects of second-generation antipsychotics
- Intracranial hypertension in pediatric patients treated with recombinant human growth hormone: data from 25 years of the Genentech National Cooperative Growth Study
- Effects of recombinant human growth hormone on protein turnover in the fasting and fed state in adolescents with Crohn disease
- Circular IGFBP-3 level affected by the gene transfer of different growth hormone isoforms
- Changes in plasma FGF23 in growth hormone deficient children during rhGH therapy
- Insulin-like growth factor-1 (IGF-1) serum concentration among 7-year-old extremely low birth weight children – an indicator of growth problems
- The effect of the length of the prodromal period on the metabolic control within the first 2 years in children with diabetic ketoacidosis manifestation
- Clinical characteristics at presentation of type 1 diabetes mellitus in children younger than 15 years in Croatia
- Umbilical cord oxidative stress in infants of diabetic mothers and its relation to maternal hyperglycemia
- The relationship between serum magnesium levels wıth childhood obesity and insulin resistance: a review of the literature
- Fulminant type 1 diabetes mellitus in Korean adolescents
- Retinol-binding protein 4 correlates with triglycerides but not insulin resistance in prepubertal children with and without premature adrenarche
- The energy expenditure of an activity-promoting video game compared to sedentary video games and TV watching
- Acanthosis nigricans and truncal fat in overweight and obese children
- The effects of antiepileptic drugs on the relationships between leptin levels and bone turnover in prepubertal children with epilepsy
- The association between morning cortisol and adiposity in children varies by weight status
- Evaluation of two dietary treatments in obese hyperinsulinemic adolescents
- Early cardiac abnormalities and serum N-terminal pro B-type natriuretic peptide levels in obese children
- Multivariate analyses of factors that affect neonatal screening thyroid stimulating hormone
- Establishment of reference range of plasma amino acids for younger Chinese children by reverse phase HPLC
- Differentiated thyroid carcinomas in childhood: clinicopathologic results of 26 patients
- Differentiated thyroid carcinoma: presentation and follow-up in children and adolescents
- Two cases of Fanconi-Bickel syndrome: first report from China with novel mutations of SLC2A2 gene
- Short Communications
- Idiopathic Fanconi’s syndrome with nephrogenic diabetes insipidus in a child who presented as vitamin D resistant rickets – a case report and review of literature
- U.S. News and World Report’s rankings of the top 50 children’s hospitals for diabetes and endocrinology reflect reputation more than objective measures
- Patient Reports
- A V59M KCNJ11 gene mutation leading to intermediate DEND syndrome in a Chinese child
- Congenital hypopituitarism presenting as dilated cardiomyopathy in a child
- Seventeen-year-old adolescent with pituitary abscess
- Blastomycosis of the central nervous system in a child: a rare cause of hypopituitarism
- A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies
- Poorly differentiated thyroid carcinoma in a 9-year-old boy: case report
- Congenital hypothyroidism in association with chromosome 3p25.3-pter deletion
- Membranoproliferative glomerulonephritis associated with autoimmune thyroiditis
- Report of two unrelated patients with hereditary vitamin D resistant rickets due to the same novel mutation in the vitamin D receptor
- Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports
- A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus
- From idiopathic diabetes insipidus to neurodegenerative Langerhans cell histiocytosis – an unusual presentation and progression of disease
- Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes
- Hyperinsulinism associated with gestational exposure to bupropion in a newborn infant
- Child abuse suspicion masquerading new onset insulin dependent diabetes mellitus
- Identification of two novel BCKDHA mutations in a Chinese patient with maple syrup urine disease
- Unexpected finding of an intact distal vagina in an infant with mixed gonadal dysgenesis
- Acrogigantism and facial asymmetry: McCune-Albright syndrome
- Surgical enucleation of testicular leydigioma in a young child: case report and literature review
- A rare case of severe lactic acidosis in a preterm infant: lack of thiamine during total parenteral nutrition
- Autoimmune polyendocrinopathy associated with ring chromosome 18
- SADDAN syndrome
- Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation
- Letters to the Editor
- Maple syrup urine disease in mainland China
- Evidence does not support the conclusion that soy is an endocrine disruptor
- Medical iodophobia is contagious
- Meetings
- Meetings Calendar
Artikel in diesem Heft
- Editorial
- IGF-I in extremely low birth weight (ELBW): a long-term observation
- Original Articles
- A potential role for adjunctive vitamin D therapy in the management of weight gain and metabolic side effects of second-generation antipsychotics
- Intracranial hypertension in pediatric patients treated with recombinant human growth hormone: data from 25 years of the Genentech National Cooperative Growth Study
- Effects of recombinant human growth hormone on protein turnover in the fasting and fed state in adolescents with Crohn disease
- Circular IGFBP-3 level affected by the gene transfer of different growth hormone isoforms
- Changes in plasma FGF23 in growth hormone deficient children during rhGH therapy
- Insulin-like growth factor-1 (IGF-1) serum concentration among 7-year-old extremely low birth weight children – an indicator of growth problems
- The effect of the length of the prodromal period on the metabolic control within the first 2 years in children with diabetic ketoacidosis manifestation
- Clinical characteristics at presentation of type 1 diabetes mellitus in children younger than 15 years in Croatia
- Umbilical cord oxidative stress in infants of diabetic mothers and its relation to maternal hyperglycemia
- The relationship between serum magnesium levels wıth childhood obesity and insulin resistance: a review of the literature
- Fulminant type 1 diabetes mellitus in Korean adolescents
- Retinol-binding protein 4 correlates with triglycerides but not insulin resistance in prepubertal children with and without premature adrenarche
- The energy expenditure of an activity-promoting video game compared to sedentary video games and TV watching
- Acanthosis nigricans and truncal fat in overweight and obese children
- The effects of antiepileptic drugs on the relationships between leptin levels and bone turnover in prepubertal children with epilepsy
- The association between morning cortisol and adiposity in children varies by weight status
- Evaluation of two dietary treatments in obese hyperinsulinemic adolescents
- Early cardiac abnormalities and serum N-terminal pro B-type natriuretic peptide levels in obese children
- Multivariate analyses of factors that affect neonatal screening thyroid stimulating hormone
- Establishment of reference range of plasma amino acids for younger Chinese children by reverse phase HPLC
- Differentiated thyroid carcinomas in childhood: clinicopathologic results of 26 patients
- Differentiated thyroid carcinoma: presentation and follow-up in children and adolescents
- Two cases of Fanconi-Bickel syndrome: first report from China with novel mutations of SLC2A2 gene
- Short Communications
- Idiopathic Fanconi’s syndrome with nephrogenic diabetes insipidus in a child who presented as vitamin D resistant rickets – a case report and review of literature
- U.S. News and World Report’s rankings of the top 50 children’s hospitals for diabetes and endocrinology reflect reputation more than objective measures
- Patient Reports
- A V59M KCNJ11 gene mutation leading to intermediate DEND syndrome in a Chinese child
- Congenital hypopituitarism presenting as dilated cardiomyopathy in a child
- Seventeen-year-old adolescent with pituitary abscess
- Blastomycosis of the central nervous system in a child: a rare cause of hypopituitarism
- A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies
- Poorly differentiated thyroid carcinoma in a 9-year-old boy: case report
- Congenital hypothyroidism in association with chromosome 3p25.3-pter deletion
- Membranoproliferative glomerulonephritis associated with autoimmune thyroiditis
- Report of two unrelated patients with hereditary vitamin D resistant rickets due to the same novel mutation in the vitamin D receptor
- Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports
- A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus
- From idiopathic diabetes insipidus to neurodegenerative Langerhans cell histiocytosis – an unusual presentation and progression of disease
- Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes
- Hyperinsulinism associated with gestational exposure to bupropion in a newborn infant
- Child abuse suspicion masquerading new onset insulin dependent diabetes mellitus
- Identification of two novel BCKDHA mutations in a Chinese patient with maple syrup urine disease
- Unexpected finding of an intact distal vagina in an infant with mixed gonadal dysgenesis
- Acrogigantism and facial asymmetry: McCune-Albright syndrome
- Surgical enucleation of testicular leydigioma in a young child: case report and literature review
- A rare case of severe lactic acidosis in a preterm infant: lack of thiamine during total parenteral nutrition
- Autoimmune polyendocrinopathy associated with ring chromosome 18
- SADDAN syndrome
- Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation
- Letters to the Editor
- Maple syrup urine disease in mainland China
- Evidence does not support the conclusion that soy is an endocrine disruptor
- Medical iodophobia is contagious
- Meetings
- Meetings Calendar