PlumX Metrics
Embed PlumX Metrics

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
  • 934
    Citations
  • 0
    Usage
  • 740
    Captures
  • 9
    Mentions
  • 11
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    934
    • Citation Indexes
      910
    • Policy Citations
      17
      • Policy Citation
        17
    • Clinical Citations
      7
      • PubMed Guidelines
        7
  • Captures
    740
  • Mentions
    9
    • References
      6
      • Wikipedia
        6
    • News Mentions
      3
      • News
        3
  • Social Media
    11
    • Shares, Likes & Comments
      11
      • Facebook
        11

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

Speiser, Phyllis W; Azziz, Ricardo; Baskin, Laurence S; Ghizzoni, Lucia; Hensle, Terry W; Merke, Deborah P; Meyer-Bahlburg, Heino F L; Miller, Walter L; Montori, Victor M; Oberfield, Sharon E; Ritzen, Martin; White, Perrin C; Endocrine Society

The Endocrine Society

Medicine; Biochemistry, Genetics and Molecular Biology

Provide Feedback

Have ideas for a new metric? Would you like to see something else here?Let us know