222 related articles for article (PubMed ID: 6977282)
1. Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.
Chrousos GP; Loriaux DL; Mann DL; Cutler GB
Ann Intern Med; 1982 Feb; 96(2):143-8. PubMed ID: 6977282
[TBL] [Abstract][Full Text] [Related]
2. Adult manifestation of congenital adrenal hyperplasia due to incomplete 21-hydroxylase deficiency mimicking polycystic ovarian disease.
Lobo RA; Goebelsmann U
Am J Obstet Gynecol; 1980 Nov; 138(6):720-6. PubMed ID: 6254362
[TBL] [Abstract][Full Text] [Related]
3. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
Chrousos GP; Loriaux DL; Mann D; Cutler GB
Horm Res; 1982; 16(4):193-200. PubMed ID: 6290362
[TBL] [Abstract][Full Text] [Related]
4. The phenotype of hirsute women: a comparison of polycystic ovary syndrome and 21-hydroxylase-deficient nonclassic adrenal hyperplasia.
Pall M; Azziz R; Beires J; Pignatelli D
Fertil Steril; 2010 Jul; 94(2):684-9. PubMed ID: 19726039
[TBL] [Abstract][Full Text] [Related]
5. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
Migeon CJ; Rosenwaks Z; Lee PA; Urban MD; Bias WB
J Clin Endocrinol Metab; 1980 Sep; 51(3):647-9. PubMed ID: 6251108
[TBL] [Abstract][Full Text] [Related]
6. Non-classic adrenal hyperplasia due to the deficiency of 21-hydroxylase and its relation to polycystic ovarian syndrome.
Pignatelli D
Front Horm Res; 2013; 40():158-70. PubMed ID: 24002412
[TBL] [Abstract][Full Text] [Related]
7. [Hirsutism: differential diagnosis].
Marcondes JA
Arq Bras Endocrinol Metabol; 2006 Dec; 50(6):1108-16. PubMed ID: 17221119
[TBL] [Abstract][Full Text] [Related]
8. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Lee PA; Rosenwaks Z; Urban MD; Migeon CJ; Bias WD
J Clin Endocrinol Metab; 1982 Nov; 55(5):866-71. PubMed ID: 6288754
[TBL] [Abstract][Full Text] [Related]
9. The prevalence of late onset congenital adrenal hyperplasia in hirsute women from Central Anatolia.
Kamel N; Tonyukuk V; Emral R; Corapçioğlu D; Baştemir M; Güllü S
Endocr J; 2003 Dec; 50(6):815-23. PubMed ID: 14709856
[TBL] [Abstract][Full Text] [Related]
10. The endocrine pattern of late onset adrenal hyperplasia (21-hydroxylase deficiency).
Carmina E; Gagliano AM; Rosato F; Maggiore M; Jannì A
J Endocrinol Invest; 1984 Apr; 7(2):89-92. PubMed ID: 6327799
[TBL] [Abstract][Full Text] [Related]
11. The prevalence of non-classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Greek women with hirsutism and polycystic ovary syndrome.
Trakakis E; Rizos D; Loghis C; Chryssikopoulos A; Spyropoulou M; Salamalekis E; Simeonides G; Vagopoulos V; Salamalekis G; Kassanos D
Endocr J; 2008 Mar; 55(1):33-9. PubMed ID: 18187875
[TBL] [Abstract][Full Text] [Related]
12. [21-Hydroxylase deficiency. Clinical expression of heterozygote carriers in a family].
Colle M; Battin J
Arch Fr Pediatr; 1984; 41(7):483-5. PubMed ID: 6333857
[TBL] [Abstract][Full Text] [Related]
13. [Partial deficiency in 21-hydroxylase in certain forms of hirsutism].
Lucisano A; Satta MA; Tripodi R; Mobili L; De Cicco F; Monaco F; Dell'Acqua S; Roche J
C R Seances Soc Biol Fil; 1989; 183(2):117-21. PubMed ID: 2555033
[TBL] [Abstract][Full Text] [Related]
14. 21-Hydroxylase deficiency in female hyperandrogenism: screening and diagnosis.
Azziz R; Zacur HA
J Clin Endocrinol Metab; 1989 Sep; 69(3):577-84. PubMed ID: 2547827
[TBL] [Abstract][Full Text] [Related]
15. The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women.
Chetkowski RJ; DeFazio J; Shamonki I; Judd HL; Chang RJ
J Clin Endocrinol Metab; 1984 Apr; 58(4):595-8. PubMed ID: 6321532
[TBL] [Abstract][Full Text] [Related]
16. The prevalence, molecular analysis and HLA typing of late-onset 21-hydroxylase deficiency in Turkish woman with hirsutism and polycystic ovary.
Yarman S; Dursun A; Oguz F; Alagol F
Endocr J; 2004 Feb; 51(1):31-6. PubMed ID: 15004406
[TBL] [Abstract][Full Text] [Related]
17. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
Kohn B; Levine LS; Pollack MS; Pang S; Lorenzen F; Levy D; Lerner AJ; Rondanini GF; Dupont B; New MI
J Clin Endocrinol Metab; 1982 Nov; 55(5):817-27. PubMed ID: 6288753
[TBL] [Abstract][Full Text] [Related]
18. Late-onset congenital adrenal hyperplasia with Cushing syndrome.
Erdogan G; Pabuccu R; Ertek S; Israel S; Yilmaz B; Yilmaz H; Caglar G
Intern Med; 2014; 53(17):1955-9. PubMed ID: 25175129
[TBL] [Abstract][Full Text] [Related]
19. Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency.
Dewailly D; Vantyghem-Haudiquet MC; Sainsard C; Buvat J; Cappoen JP; Ardaens K; Racadot A; Lefebvre J; Fossati P
J Clin Endocrinol Metab; 1986 Aug; 63(2):418-23. PubMed ID: 3013919
[TBL] [Abstract][Full Text] [Related]
20. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism.
Siegel SF; Finegold DN; Lanes R; Lee PA
N Engl J Med; 1990 Sep; 323(13):849-54. PubMed ID: 2168515
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
