Literature DB >> 6257014

Congenital adrenal hyperplasia due to partial 21-hydroxylase deficiency. A study of five cases.

P Bouchard, F Kuttenn, I Mowszowicz, G Schaison, M C Raux-Eurin, P Mauvais-Jarvis.   

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Year:  1981        PMID： 6257014     DOI： 10.1530/acta.0.0960107

Source DB:  PubMed          Journal:  Acta Endocrinol (Copenh)        ISSN： 0001-5598


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  4 in total

Review 1.  Hirsutism: pilosebaceous unit dysregulation. Role of peripheral and glandular factors.

Authors:  V Toscano
Journal:  J Endocrinol Invest       Date:  1991-02       Impact factor: 4.256

2.  HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).

Authors:  C Scaroni; E Orlandini; C Venturi Pasini; M Gangemi; F Mantero
Journal:  J Endocrinol Invest       Date:  1986-02       Impact factor: 4.256

3.  The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).

Authors:  E Carmina; A M Gagliano; F Rosato; M Maggiore; A Jannì
Journal:  J Endocrinol Invest       Date:  1984-04       Impact factor: 4.256

4.  Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study.

Authors:  B J Manfras; M Swinyard; W A Rudert; E J Ball; P A Lee; P Kühnl; M Trucco; B O Böhm
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132
  4 in total

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