Works matching IS 0334018X AND DT 2022 AND VI 35 AND IP 9
Results: 16
Frontmatter.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. i, doi. 10.1515/jpem-2022-frontmatter1
- Publication type:
- Article
The mediating function of obesity on endocrine-disrupting chemicals and insulin resistance in children.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1169, doi. 10.1515/jpem-2022-0354
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- Article
Pattern of presentation of paediatric endocrine disorders in a Nigerian tertiary institution: an 11-year survey.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1183, doi. 10.1515/jpem-2022-0300
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- Article
Diabetic ketoacidosis in children with new-onset type 1 diabetes mellitus: demographics, risk factors and outcome: an 11 year review in Hong Kong.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1132, doi. 10.1515/jpem-2022-0255
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- Article
Effects and dose-response relationships of exercise intervention on weight loss in overweight and obese children: a meta-regression and system review.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1117, doi. 10.1515/jpem-2022-0209
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- Article
Severe loss of adipose tissue in a Vietnamese lipodystrophy patient caused by LMNA p.G465D mutation: a first clinical characterization and two-year follow-up.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1206, doi. 10.1515/jpem-2022-0208
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- Article
Universal salt iodization potentially contributes to health equity: socio-economic status of children does not affect iodine status.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1154, doi. 10.1515/jpem-2022-0166
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- Article
Identification of two novel ACAT1 variant associated with beta-ketothiolase deficiency in a 9-month-old boy.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1194, doi. 10.1515/jpem-2022-0158
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- Article
Association between clinical variations and copy number variations in cases with Turner syndrome.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1161, doi. 10.1515/jpem-2022-0153
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- Article
Craniosynostosis in a patient with Fanconi–Bickel syndrome: a case report.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1201, doi. 10.1515/jpem-2022-0150
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- Publication type:
- Article
Novel non-stop variant of the NR0B1 gene in two siblings with adrenal hypoplasia congenita.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1189, doi. 10.1515/jpem-2022-0120
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- Publication type:
- Article
Incidence tendency, etiological classification and outcome of congenital hypothyroidism in Guangzhou, China: an 11-year retrospective population-based study.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1141, doi. 10.1515/jpem-2022-0107
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- Article
Relationship between prolactin level and puberty in girls with early breast development.
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- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1177, doi. 10.1515/jpem-2022-0093
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- Article
Metabolically healthy obesity in a paediatric obesity clinic.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1147, doi. 10.1515/jpem-2022-0086
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- Publication type:
- Article
The response to growth hormone treatment in a child with short stature, growth hormone deficiency and autosomal dominant cutis laxa type 3 – case report.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1211, doi. 10.1515/jpem-2022-0054
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- Article
Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2022, v. 35, n. 9, p. 1215, doi. 10.1515/jpem-2021-0717
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- Article