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3. 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]
4. Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Khandekar S; Lata V; Dash RJ Indian J Med Res; 1990 Apr; 92():79-82. PubMed ID: 2164496 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis]. Lambotte C Rev Med Liege; 1986 Jan; 41(2):37-44. PubMed ID: 3006204 [No Abstract] [Full Text] [Related]
7. 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]
8. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study. Kauschansky A; Kaufman H; Zamir R; Elian E Horm Res; 1981; 14(2):73-8. PubMed ID: 6268517 [No Abstract] [Full Text] [Related]
9. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients. Livieri C; Belvedere M; Martinetti M; Beluffi G; Fiori P; Cogliati CR; Goffredo V; Lorini R; Severi F Prog Clin Biol Res; 1985; 200():243-55. PubMed ID: 3001775 [No Abstract] [Full Text] [Related]
11. Assessment of the one hour adrenocorticotrophic hormone test in the diagnosis of attenuated 21-hydroxylase deficiency. Innanen VT; Vale JM J Clin Pathol; 1990 Jun; 43(6):493-5. PubMed ID: 2166094 [TBL] [Abstract][Full Text] [Related]
12. "Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasia. New MI; Lorenzen F; Pang S; Gunczler P; Dupont B; Levine LS J Clin Endocrinol Metab; 1979 Feb; 48(2):356-9. PubMed ID: 218988 [TBL] [Abstract][Full Text] [Related]
13. Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Gutai JP; Lee PA; Johnsonbaugh RE; Gareis F; Urban MD; Migeon CJ J Pediatr; 1979 May; 94(5):770-2. PubMed ID: 221633 [No Abstract] [Full Text] [Related]
14. Failure of angiotensin II to stimulate increases in concentrations of adrenal androgens, 17-hydroxyprogesterone, or adrenocorticotropin in congenital 21-hydroxylase deficiency. Wisgerhof M; Mellinger RC; Zafar MS J Clin Endocrinol Metab; 1983 Mar; 56(3):627-31. PubMed ID: 6296191 [TBL] [Abstract][Full Text] [Related]
15. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency. Stuckey MS; Boyne P; Macdonald WB; Christiansen FT; Houliston JB; Dawkins RL Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552 [TBL] [Abstract][Full Text] [Related]
16. Circadian variation of plasma 17-hydroxyprogesterone among heterozygotic carriers of 21-hydroxylase deficiency (salt-losing form). Urban MD; Migeon CJ; Lee PA Horm Res; 1986; 23(2):74-7. PubMed ID: 3484712 [TBL] [Abstract][Full Text] [Related]
17. Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasia. Pang S; Levine LS; Lorenzen F; Chow D; Pollack M; Dupont B; Genel M; New MI J Clin Endocrinol Metab; 1980 Mar; 50(3):586-9. PubMed ID: 6244328 [TBL] [Abstract][Full Text] [Related]
18. Evidence for partial 21-hydroxylase deficiency among heterozygote carriers of congenital adrenal hyperplasia. Lee PA; Gareis JF J Clin Endocrinol Metab; 1975 Aug; 41(2):415-8. PubMed ID: 169282 [TBL] [Abstract][Full Text] [Related]