PATHOPHYSIOLOGY, GENETICS, AND TREATMENT OF HYPERANDROGENISM
Pediatric Clinics of North America, ISSN: 0031-3955, Vol: 44, Issue: 2, Page: 375-395
1997
- 20Citations
- 10Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations20
- Citation Indexes20
- 20
- CrossRef9
- Captures10
- Readers10
- 10
Article Description
Hirsutism and virilism are common presenting complaints of many patients. Hirsutism may include generalized increases in body hair and may be idiopathic, genetic, or induced by drugs. Drug-induced hirsutism, or hypertrichosis, does not follow the bodily distribution of the hair associated with male secondary sexual characteristics. By contrast, virilism is mediated by androgens; therefore, an understanding of androgen biosynthesis must underlie any consideration of disorders of hyperandrogenism. Hyperandrogenic disorders can present in childhood as contrasexual virilization in girls or as precocious pseudopuberty in boys. With the exception of very rare androgen-secreting tumors and a rare genetic disorder of gonadotropin receptors, these disorders are caused by genetic lesions in the enzymes for steroid hormone synthesis.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S003139550570482X; http://dx.doi.org/10.1016/s0031-3955(05)70482-x; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0031003932&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/9130926; http://linkinghub.elsevier.com/retrieve/pii/S003139550570482X; http://api.elsevier.com/content/article/PII:S003139550570482X?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S003139550570482X?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S003139550570482X; http://dx.doi.org/10.1016/s0031-3955%2805%2970482-x; https://dx.doi.org/10.1016/s0031-3955%2805%2970482-x
Elsevier BV
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