Works matching IS 0334018X AND DT 2011 AND VI 24 AND IP 5/6
Results: 64
A newborn case with perinatal-lethal Gaucher disease due to R463H homozygosity complicated by C677T homozygosity in the MTHFR gene.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 381, doi. 10.1515/jpem.2011.001
- By:
- Publication type:
- Article
Girls with early puberty attain a near-final height similar to their target height.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 339, doi. 10.1515/jpem.2011.005
- By:
- Publication type:
- Article
Rare hypertension as a result of 17α-hydroxylase deficiency.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 333, doi. 10.1515/jpem.2011.008
- By:
- Publication type:
- Article
Childhood obesity: evidence of an association between plasminogen activator inhibitor-1 levels and visceral adiposity.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 361, doi. 10.1515/jpem.2011.015
- By:
- Publication type:
- Article
Glargine basal-bolus insulin regimen versus insulin pump therapy: comparison of glycemic control.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 369, doi. 10.1515/jpem.2011.018
- By:
- Publication type:
- Article
Endocrine complications following pediatric bone marrow transplantation.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 327, doi. 10.1515/jpem.2011.021
- By:
- Publication type:
- Article
Familial glucocorticoid deficiency due to compound heterozygosity of two novel MC2R mutations.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 395, doi. 10.1515/jpem.2011.024
- By:
- Publication type:
- Article
Benign transient hyperphosphatasemia in infants and children: a prospective cohort.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 351, doi. 10.1515/jpem.2011.025
- By:
- Publication type:
- Article
Are adolescent weight-related problems and general well-being essentially an issue of age, gender or rather a pubertal timing issue?
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 251, doi. 10.1515/jpem.2011.027
- By:
- Publication type:
- Article
Puberty and pubertal growth dynamics in children with idiopathic short stature.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 319, doi. 10.1515/jpem.2011.031
- By:
- Publication type:
- Article
Hyperthyroidism presenting with hyperglycemia in an adolescent female.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 385, doi. 10.1515/jpem.2011.032
- By:
- Publication type:
- Article
Plasma leptin and adiponectin concentrations in healthy, non-obese children.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 313, doi. 10.1515/jpem.2011.037
- By:
- Publication type:
- Article
Dorsolumbar kyphosis: diagnostic value of hook shaped vertebra.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 249, doi. 10.1515/jpem.2011.040
- By:
- Publication type:
- Article
Letter to the Editor.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 399, doi. 10.1515/jpem.2011.046
- By:
- Publication type:
- Article
Vitamin D receptor genotypes are associated with bone mass in patients with Turner syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 307, doi. 10.1515/jpem.2011.047
- By:
- Publication type:
- Article
Growth suppression caused by corticosteroid eye drops.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 393, doi. 10.1515/jpem.2011.048
- By:
- Publication type:
- Article
HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 377, doi. 10.1515/jpem.2011.049
- By:
- Publication type:
- Article
Causes and patterns of referral to a tertiary, multidisciplinary program for the treatment of childhood obesity.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 303, doi. 10.1515/jpem.2011.051
- By:
- Publication type:
- Article
The relation between 25-hydroxyvitamin D with peak bone mineral density and body composition in healthy young adults.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 355, doi. 10.1515/jpem.2011.052
- By:
- Publication type:
- Article
Meetings Calendar.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 401, doi. 10.1515/jpem.2011.132
- Publication type:
- Article
Publisher's Note.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 245, doi. 10.1515/jpem.2011.133
- Publication type:
- Article
The damage caused by incomplete and uncontrolled medical information.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 247, doi. 10.1515/jpem.2011.134
- By:
- Publication type:
- Article
A new heterozygous mutation (D196N) in the Gs alpha gene as a cause for pseudohypoparathyroidism type IA in a boy who had gallstones.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 297, doi. 10.1515/jpem.2011.172
- By:
- Publication type:
- Article
The role of metabolic syndrome components and adipokines in insulin resistance in prepubertal children.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 289, doi. 10.1515/jpem.2011.177
- By:
- Publication type:
- Article
A case of McCune-Albright syndrome associated with pituitary GH adenoma: therapeutic process and autopsy.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 283, doi. 10.1515/jpem.2011.178
- By:
- Publication type:
- Article
Persistent hyperthyrotropinemia in congenital hypothyroidism: successful combination treatment with levothyroxine and liothyronine.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 347, doi. 10.1515/jpem.2011.179
- By:
- Publication type:
- Article
Treatment of symptomatic osteoporosis in children: a comparison of two pamidronate dosage regimens.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 271, doi. 10.1515/jpem.2011.182
- By:
- Publication type:
- Article
Stanozolol regulates proliferation of growth plate chondrocytes via activation of ERα in GnRHa-treated adolescent rats.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 275, doi. 10.1515/jpem.2011.183
- By:
- Publication type:
- Article
A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitus.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 373, doi. 10.1515/jpem.2011.187
- By:
- Publication type:
- Article
The effect of glucocorticoid replacement therapy on bone mineral density in children with congenital adrenal hyperplasia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 265, doi. 10.1515/jpem.2011.189
- By:
- Publication type:
- Article
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.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 257, doi. 10.1515/jpem.2011.194
- By:
- Publication type:
- Article
A single base-pair deletion in the WFS1 gene causes Wolfram syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 389, doi. 10.1515/jpem.2011.215
- By:
- Publication type:
- Article
Meetings Calendar.
- Published in:
- 2011
- Publication type:
- Calendar
Letter to the Editor.
- Published in:
- 2011
- By:
- Publication type:
- Letter to the Editor
Familial glucocorticoid deficiency due to compound heterozygosity of two novel MC2R mutations.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Growth suppression caused by corticosteroid eye drops.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
A single base-pair deletion in the WFS1 gene causes Wolfram syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 389, doi. 10.1515/JPEM.2011.215
- By:
- Publication type:
- Article
Hyperthyroidism presenting with hyperglycemia in an adolescent female.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
A newborn case with perinatal-lethal Gaucher disease due to R463H homozygosity complicated by C677T homozygosity in the MTHFR gene.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitus.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
Glargine basal-bolus insulin regimen versus insulin pump therapy: comparison of glycemic control.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 369, doi. 10.1515/JPEM.2011.018
- By:
- Publication type:
- Article
Childhood obesity: evidence of an association between plasminogen activator inhibitor-1 levels and visceral adiposity.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 361, doi. 10.1515/JPEM.2011.015
- By:
- Publication type:
- Article
The relation between 25-hydroxyvitamin D with peak bone mineral density and body composition in healthy young adults.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 355, doi. 10.1515/JPEM.2011.052
- By:
- Publication type:
- Article
Benign transient hyperphosphatasemia in infants and children: a prospective cohort.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 351, doi. 10.1515/JPEM.2011.025
- By:
- Publication type:
- Article
Persistent hyperthyrotropinemia in congenital hypothyroidism: successful combination treatment with levothyroxine and liothyronine.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 347, doi. 10.1515/JPEM.2011.179
- By:
- Publication type:
- Article
Girls with early puberty attain a near-fi nal height similar to their target height.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 339, doi. 10.1515/JPEM.2011.005
- By:
- Publication type:
- Article
Rare hypertension as a result of 17 α -hydroxylase deficiency.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 333, doi. 10.1515/JPEM.2011.008
- By:
- Publication type:
- Article
Endocrine complications following pediatric bone marrow transplantation.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 327, doi. 10.1515/JPEM.2011.021
- By:
- Publication type:
- Article
Puberty and pubertal growth dynamics in children with idiopathic short stature.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 5/6, p. 319, doi. 10.1515/JPEM.2011.031
- By:
- Publication type:
- Article