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Frontmatter.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. i, doi. 10.1515/jpem-2019-frontmatter11
- Publication type:
- Article
Hypo- and hyperthyroidism in early life – new developments.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1199, doi. 10.1515/jpem-2019-0509
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- Article
Optic nerve sheath diameter appraisal in children affected by diabetic ketoacidosis.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1203, doi. 10.1515/jpem-2019-0371
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- Article
Optic nerve sheath diameter ultrasound measurement to evaluate cerebral edema in children with diabetic ketoacidosis.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1205, doi. 10.1515/jpem-2019-0333
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- Article
Novel ABCD1 gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1207, doi. 10.1515/jpem-2019-0244
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- Article
Phenylketonuric patients represent their disease.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1217, doi. 10.1515/jpem-2019-0253
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- Publication type:
- Article
Mapping of IDUA gene variants in Pakistani patients with mucopolysaccharidosis type 1.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1221, doi. 10.1515/jpem-2019-0188
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- Publication type:
- Article
Genetic testing of two Pakistani patients affected with rare autosomal recessive Fanconi-Bickel syndrome and identification of a novel SLC2A2 splice site variant.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1229, doi. 10.1515/jpem-2019-0235
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- Publication type:
- Article
Sex differences in infant body composition emerge in the first 5 months of life.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1235, doi. 10.1515/jpem-2019-0243
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- Publication type:
- Article
Characterization of the duration of treatment with diazoxide in infants with prolonged hyperinsulinism (PHI).
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1241, doi. 10.1515/jpem-2019-0066
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- Article
Clinical, biochemical and gender characteristics of 97 prepubertal children with premature adrenarche.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1247, doi. 10.1515/jpem-2019-0185
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- Publication type:
- Article
The adjustment of 17-hydroxyprogesterone cut-off values for congenital adrenal hyperplasia neonatal screening by GSP according to gestational age and age at sampling.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1253, doi. 10.1515/jpem-2019-0140
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- Publication type:
- Article
The role of vitamin D replacement therapy in serum FGF23 concentration in children with myelomeningocele compared with healthy children – a preliminary study.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1259, doi. 10.1515/jpem-2018-0509
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- Article
Genetic analyses in a cohort of Portuguese pediatric patients with congenital hypothyroidism.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1265, doi. 10.1515/jpem-2019-0047
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- Publication type:
- Article
Congenital hypothyroidism in preterm infants: a 3- to 8-year longitudinal study in southern Thailand.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1275, doi. 10.1515/jpem-2019-0054
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- Publication type:
- Article
A case of PHACE syndrome with growth hormone deficiency and abnormal thyroid functions.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1283, doi. 10.1515/jpem-2019-0078
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- Publication type:
- Article
A novel DCAF17 homozygous mutation in a girl with Woodhouse-Sakati syndrome and review of the current literature.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1287, doi. 10.1515/jpem-2019-0173
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- Publication type:
- Article
Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girl.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1295, doi. 10.1515/jpem-2019-0082
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- Article
Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case report.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 11, p. 1299, doi. 10.1515/jpem-2019-0051
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- Article