Works matching IS 0334018X AND DT 2019 AND VI 32 AND IP 3
Results: 16
Frontmatter.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. i, doi. 10.1515/jpem-2019-frontmatter2
- Publication type:
- Article
The effect of PKU diet on the maternal quality of life and social discrimination in relation to their educational status and place of living.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 281, doi. 10.1515/jpem-2018-0525
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- Article
Studying the effect of large neutral amino acid supplements on oxidative stress in phenylketonuric patients.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 269, doi. 10.1515/jpem-2018-0454
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- Article
Evaluating the four most important salivary sex steroids during male puberty: testosterone best characterizes pubertal development.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 287, doi. 10.1515/jpem-2018-0451
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- Article
Adiposity and adipocytokines: the moderator role of cardiorespiratory fitness and pubertal stage in girls.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 239, doi. 10.1515/jpem-2018-0407
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- Article
Validation of the Greek version of the Quality of Life in Short Stature Youth (QoLISSY) questionnaire.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 215, doi. 10.1515/jpem-2018-0403
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- Publication type:
- Article
A rare case of congenital hyperinsulinism (CHI) due to dual genetic aetiology involving HNF4A and ABCC8.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 301, doi. 10.1515/jpem-2018-0389
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- Publication type:
- Article
Identification of two novel TPK1 gene mutations in a Chinese patient with thiamine pyrophosphokinase deficiency undergoing whole exome sequencing.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 295, doi. 10.1515/jpem-2018-0363
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- Publication type:
- Article
The effect of therapy on plasma ghrelin and leptin levels, and appetite in children with iron deficiency anemia.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 275, doi. 10.1515/jpem-2018-0352
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- Publication type:
- Article
A pilot study on newborn screening for congenital adrenal hyperplasia in Beijing.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 253, doi. 10.1515/jpem-2018-0342
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- Publication type:
- Article
Cinacalcet therapy in an infant with an R185Q calcium-sensing receptor mutation causing hyperparathyroidism: a case report and review of the literature.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 305, doi. 10.1515/jpem-2018-0307
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- Publication type:
- Article
Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 259, doi. 10.1515/jpem-2018-0298
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- Publication type:
- Article
Serum omentin-1 levels in obese children.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 247, doi. 10.1515/jpem-2018-0231
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- Publication type:
- Article
Physical growth and development characteristics of children with Williams syndrome aged 0–24 months in Zhejiang Province.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 233, doi. 10.1515/jpem-2018-0185
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- Publication type:
- Article
Improved adherence and growth outcomes with jet-delivered growth hormone.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 207, doi. 10.1515/jpem-2018-0067
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- Publication type:
- Article
Growth hormone deficiency in children with antenatal Bartter syndrome.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 3, p. 225, doi. 10.1515/jpem-2018-0188
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- Publication type:
- Article