Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
Journal of Clinical Endocrinology and Metabolism, ISSN: 0021-972X, Vol: 95, Issue: 9, Page: 4133-4160
2010
- 934Citations
- 740Captures
- 9Mentions
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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.
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
- Citations934
- Citation Indexes910
- 910
- CrossRef352
- Policy Citations17
- Policy Citation17
- Clinical Citations7
- PubMed Guidelines7
- Captures740
- Readers740
- 739
- Mentions9
- References6
- Wikipedia6
- News Mentions3
- News3
Most Recent News
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency in South Africa.(RESEARCH)(Report)
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders characterised by enzyme deficiencies that impair adrenal steroid biosynthesis. The most common form is
Article Description
We developed clinical practice guidelines for congenital adrenal hyperplasia (CAH).
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021972X10606829; http://dx.doi.org/10.1210/jc.2009-2631; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77956588420&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/20823466; https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.2009-2631
The Endocrine Society
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