Adrenocorticotropic hormone testing in idiopathic hirsutism and polycystic ovarian disease: a test of limited usefulness
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference8 articles.
1. Lateonset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease: an allelic variant of congenital virilizing adrenal hyperplasia with a milder enzymatic defect;Chrousos;Ann Intern Med,1982
2. Partial 11- and 21-hydroxylase deficiencies in hirsute women;Newmark;Am J Obstet Gynecol,1977
3. The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women;Chetkowski;J Clin Endocrinol Metab,1984
4. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data;New;J Clin Endocrinol Metab,1983
5. Testicular function in Klinefelter’s syndrome;Gabrilove;J Urol,1980
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1. Differential activity of the corticosteroidogenic enzymes in normal cycling women and women with polycystic ovary syndrome;Reviews in Endocrine and Metabolic Disorders;2019-02-23
2. Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women;Human Reproduction Update;2017-06-05
3. Comparison of steroidogenic pathways among normoandrogenic and hyperandrogenic polycystic ovary syndrome patients and normal cycling women;Journal of Obstetrics and Gynaecology Research;2014-09-26
4. New insights into steroidogenesis in normo- and hyperandrogenic polycystic ovary syndrome patients;Arquivos Brasileiros de Endocrinologia & Metabologia;2013-08
5. A 31-year-old woman with infertility and polycystic ovaries diagnosed with non-classic congenital adrenal hyperplasia due to a novel CYP21 mutation;Journal of Endocrinological Investigation;2008-02
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