Works matching IS 0334018X AND DT 2014 AND VI 27 AND IP 6/10
Results: 39
Growth hormone treatment in a patient with Hurler-Scheie syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 957, doi. 10.1515/jpem-2013-0340
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- Article
Pubertal development profile in patients with Turner syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 845, doi. 10.1515/jpem-2013-0256
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- Article
The role of anti-Mullerian and inhibin B hormones in the evaluation of 46,XY disorders of sex development.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 891, doi. 10.1515/jpem-2013-0355
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- Article
Serum insulin-like growth factor-binding protein-3 level correlated with glycemic control and lipid profiles in children and adolescents with type 1 diabetes.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 857, doi. 10.1515/jpem-2013-0358
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- Article
Cushing's syndrome: hidden risk in usage of topical corticosteroids.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 977, doi. 10.1515/jpem-2013-0262
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- Article
Assessment of aortic morphology and compliance in children and adolescents with Ullrich-Turner syndrome (UTS) using magnetic resonance imaging (MRI).
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 915, doi. 10.1515/jpem-2013-0332
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- Article
A novel CASR mutation associated with neonatal severe hyperparathyroidism transmitted as an autosomal recessive disorder.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 851, doi. 10.1515/jpem-2013-0343
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- Article
The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 901, doi. 10.1515/jpem-2013-0273
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- Article
Evaluation of epicardial adipose tissue, carotid intima-media thickness and ventricular functions in obese children and adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 827, doi. 10.1515/jpem-2013-0306
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- Article
Muscle strength and body composition during the transition phase in patients treated with recombinant GH to final height.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 813, doi. 10.1515/jpem-2013-0317
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- Article
Maternal factors and complications of preterm birth associated with neonatal thyroid stimulating hormone.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 929, doi. 10.1515/jpem-2013-0366
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- Article
The effect of adenotonsilectomy on ghrelin, leptin, IGF-1 levels and growth parameters in children with adenotonsillar hypertrophy.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 885, doi. 10.1515/jpem-2013-0367
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- Article
Management of central diabetes insipidus with oral desmopressin lyophilisate in infants.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 923, doi. 10.1515/jpem-2013-0368
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- Article
Counseling patients with succinate dehydrogenase subunit defects: genetics, preventive guidelines, and dealing with uncertainty.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 837, doi. 10.1515/jpem-2013-0369
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- Article
Multiple autoimmunity, type 1 diabetes (T1DM), autoimmune thyroiditis and thyroid cancer: is there an association? A case report and literature review.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 1011, doi. 10.1515/jpem-2013-0370
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- Article
The natural course of Hashimoto's thyroiditis in children and adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 807, doi. 10.1515/jpem-2013-0373
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- Article
Berardinelli-Seip congenital lipodystrophy: an autosomal recessive disorder with rare association of duodenocolonic polyps.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 989, doi. 10.1515/jpem-2013-0399
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- Article
Benign vaginal bleeding in 24 prepubertal patients: clinical, biochemical and imaging features.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 821, doi. 10.1515/jpem-2013-0415
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- Article
Clinical applicability of rapid detection of SRY and DYS14 genes in patients with disorders of sex development using an indigenously developed 5′ exonuclease based assay.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 869, doi. 10.1515/jpem-2013-0416
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- Article
Adult human liver mesenchymal progenitor cells express phenylalanine hydroxylase.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 863, doi. 10.1515/jpem-2013-0425
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- Article
Rare case of homozygous epimerase deficiency and heterozygous of duarte 2 variant.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 947, doi. 10.1515/jpem-2013-0431
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- Article
Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 873, doi. 10.1515/jpem-2013-0443
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Towards an optimization of the management of endocrine complications of thalassemia.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 801, doi. 10.1515/jpem-2013-0444
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- Article
Ovarian hyperstimulation syndrome treated by medroxyprogesterone acetate.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 997, doi. 10.1515/jpem-2013-0452
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- Article
Ectopic Cushing syndrome secondary to metastatic medullary thyroid cancer in a child with multiple endocrine neoplasia syndrome type 2B: clues to early diagnosis of the paraneoplastic syndromes.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 993, doi. 10.1515/jpem-2013-0456
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Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 967, doi. 10.1515/jpem-2013-0469
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Persistent congenital hyperinsulinism in two patients with Beckwith-Wiedemann syndrome due to mosaic uniparental disomy 11p.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 951, doi. 10.1515/jpem-2013-0484
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- Article
Symptomatic cerebral infarction in a child with severe diabetic ketoacidosis.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 1001, doi. 10.1515/jpem-2014-0037
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- Article
Lipid patterns in treated growth hormone deficient children vs. short stature controls.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 909, doi. 10.1515/jpem-2013-0488
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- Article
Neonatal diagnosis of a patient with hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome associated with cerebral infarction.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 961, doi. 10.1515/jpem-2014-0004
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- Article
Cholestasis and protein-losing enteropathy secondary to hyperthyroidism in a 6-year-old girl.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 1017, doi. 10.1515/jpem-2014-0005
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- Article
Pubertal gynecomastia: what about the remaining 10%?
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 1027, doi. 10.1515/jpem-2014-0017
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- Article
A rare case of familial Cushing's syndrome with a common presentation of weight gain due to a mutation of the PRKAR1A gene causing isolated primary pigmented nodular adrenocortical disease.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 1005, doi. 10.1515/jpem-2014-0018
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- Article
Prader-Willi syndrome: a case report with atypical developmental features.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 983, doi. 10.1515/jpem-2013-0500
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- Article
An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 1021, doi. 10.1515/jpem-2014-0048
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- Article
Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidus.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 971, doi. 10.1515/jpem-2014-0052
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- Article
Permanent neonatal diabetes mellitus in Jordan.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 879, doi. 10.1515/jpem-2014-0069
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- Article
A rare case of pituitary infarction leading to spontaneous tumour resolution and CSF-sella syndrome in an 11-year-old girl and a review of the paediatric literature.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. 939, doi. 10.1515/jpem-2014-0143
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Frontmatter.
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- Journal of Pediatric Endocrinology & Metabolism, 2014, v. 27, n. 6/10, p. i, doi. 10.1515/jpem-2014-frontmatter9-10
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- Article