Hydrocortisone Treatment in Girls with Congenital Adrenal Hyperplasia Inhibits Serum Dehydroepiandrosterone Sulfate and Affects the GH-IGF-I System
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.2009.22.3.255/pdf
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1. Congenital Adrenal Hyperplasia
2. Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
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4. Height outcome in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency: A meta-analysis
5. Arginine normalizes the growth hormone (GH) response to GH-releasing hormone in adult patients receiving chronic daily immunosuppressive glucocorticoid therapy
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Characteristics of Growth in Children With Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency During Adrenarche and Beyond;The Journal of Clinical Endocrinology & Metabolism;2021-10-02
2. Clinical and molecular studies related to bone metabolism in patients with congenital adrenal hyperplasia;Journal of Pediatric Endocrinology and Metabolism;2014-01-15
3. IGF-I–IGFBP-3–acid-labile subunit (ALS) complex in children and adolescents with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH);Growth Hormone & IGF Research;2011-08
4. Current World Literature;Current Opinion in Endocrinology, Diabetes & Obesity;2010-06
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