Works matching IS 0334018X AND DT 2018 AND VI 31 AND IP 2
Results: 19
Identification of five mutations in a patient with galactose metabolic disorders.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 221, doi. 10.1515/jpem-2017-0438
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- Article
Improved medical-alert ID ownership and utilization in youth with congenital adrenal hyperplasia following a parent educational intervention.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 213, doi. 10.1515/jpem-2017-0435
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- Article
Decrease in serum chemerin through aerobic exercise plus dieting and its association with mitigation of cardio-metabolic risk in obese female adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 127, doi. 10.1515/jpem-2017-0431
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- Article
Insulin-mediated pseudoacromegaly: a report of two pediatric patients.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 235, doi. 10.1515/jpem-2017-0398
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- Article
Management of thyrotoxicosis in children and adolescents: 35 years’ experience in 304 patients.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 159, doi. 10.1515/jpem-2017-0394
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- Article
Associations of leptin, insulin and lipids with retinal microvasculature in children and adolescents.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 143, doi. 10.1515/jpem-2017-0374
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- Article
Association of sodium intake with insulin resistance in Korean children and adolescents: the Korea National Health and Nutrition Examination Survey 2010.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 117, doi. 10.1515/jpem-2017-0362
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- Article
Comparison between two inhibin B ELISA assays in 46,XY testicular disorders of sex development (DSD) with normal testosterone secretion.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 191, doi. 10.1515/jpem-2017-0351
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- Article
Four novel mutations of the <italic>BCKDHA</italic>, <italic>BCKDHB</italic> and <italic>DBT</italic> genes in Iranian patients with maple syrup urine disease.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 205, doi. 10.1515/jpem-2017-0305
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- Article
Association of cord blood ghrelin, leptin and insulin concentrations in term newborns with anthropometric parameters at birth.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 151, doi. 10.1515/jpem-2017-0285
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- Article
Genetic mutations associated with neonatal diabetes mellitus in Omani patients.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 195, doi. 10.1515/jpem-2017-0284
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- Article
Clinical and cytogenetic features of 516 patients with suspected Turner syndrome – a single-center experience.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 167, doi. 10.1515/jpem-2017-0273
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- Article
The role of corticosteroid-binding globulin in the evaluation of adrenal insufficiency.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 107, doi. 10.1515/jpem-2017-0270
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- Article
Ultrasonographic assessment of pubertal breast development in obese children: compliance with the clinic.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 137, doi. 10.1515/jpem-2017-0243
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- Article
Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 229, doi. 10.1515/jpem-2017-0235
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- Article
Reference centile curves for wrist circumference for Indian children aged 3–18 years.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 185, doi. 10.1515/jpem-2017-0161
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- Article
Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 175, doi. 10.1515/jpem-2017-0123
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- Article
Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 223, doi. 10.1515/jpem-2017-0095
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- Article
Novel compound heterozygous variants in the <italic>LHCGR</italic> gene identified in a subject with Leydig cell hypoplasia type 1.
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- Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 239, doi. 10.1515/jpem-2016-0445
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- Article