Works matching IS 0334018X AND DT 2016 AND VI 29 AND IP 7
Results: 20
Association between physical activity and bone in children with Prader-Willi syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 819, doi. 10.1515/jpem-2015-0233
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- Article
Pediatric thyroid nodules: ultrasonographic characteristics and inter-observer variability in prediction of malignancy.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 789, doi. 10.1515/jpem-2015-0242
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- Article
CNDP1 genotype and renal survival in pediatric nephropathies.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 827, doi. 10.1515/jpem-2015-0262
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- Article
Central diabetes insipidus as a very late relapse limited to the pituitary stalk in Langerhans cell histiocytosis.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 873, doi. 10.1515/jpem-2015-0391
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Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 841, doi. 10.1515/jpem-2015-0406
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- Article
Relationship between HOMA-IR and serum vitamin D in Chinese children and adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 777, doi. 10.1515/jpem-2015-0422
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- Article
Low 25-hydroxyvitamin D level is not an independent risk factor for hepatosteatosis in obese children.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 783, doi. 10.1515/jpem-2015-0426
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A unique case of growth hormone and human chorionic gonadotropin treatment in a 45,X male with Y: autosome translocation and literature review.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 857, doi. 10.1515/jpem-2015-0427
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Biochemical, radiological, and genetic characterization of congenital hypothyroidism in Abu Dhabi, United Arab Emirates.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 801, doi. 10.1515/jpem-2015-0275
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- Article
Childhood parathyroid adenoma: a rare but important cause of nephrolithiasis.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 853, doi. 10.1515/jpem-2015-0369
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Children with severe Osteogenesis imperfecta and short stature present on average with normal IGF-I and IGFBP-3 levels.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 813, doi. 10.1515/jpem-2015-0385
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- Article
Generic and disease-specific quality of life in adolescents with type 1 diabetes: comparison to age-matched healthy peers.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 769, doi. 10.1515/jpem-2015-0397
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- Article
Translation and psychometric properties of the Persian version of self-management of type 1 diabetes for adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 761, doi. 10.1515/jpem-2015-0403
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- Article
High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 807, doi. 10.1515/jpem-2015-0400
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- Article
Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 795, doi. 10.1515/jpem-2015-0446
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Propionic acidemia: a Turkish case report of a successful pregnancy, labor and lactation.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 863, doi. 10.1515/jpem-2015-0451
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- Article
Unusual phenotype of congenital adrenal hyperplasia (CAH) with a novel mutation of the CYP21A2 gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 867, doi. 10.1515/jpem-2015-0457
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- Article
Sertoli cell only syndrome with ambiguous genitalia.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 849, doi. 10.1515/jpem-2015-0458
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- Article
17-Hydroxyprogesterone responses to human chorionic gonadotropin are not associated with serum anti-Mullerian hormone levels among adolescent girls with polycystic ovary syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. 835, doi. 10.1515/jpem-2015-0461
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Frontmatter.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 7, p. i, doi. 10.1515/jpem-2016-frontmatter7
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- Article