326 related articles for article (PubMed ID: 2537337)
1. Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway.
Fiet J; Gueux B; Raux-DeMay MC; Kuttenn F; Vexiau P; Brerault JL; Couillin P; Galons H; Villette JM; Julien R
J Clin Endocrinol Metab; 1989 Mar; 68(3):542-7. PubMed ID: 2537337
[TBL] [Abstract][Full Text] [Related]
2. Comparison of basal and adrenocorticotropin-stimulated plasma 21-deoxycortisol and 17-hydroxyprogesterone values as biological markers of late-onset adrenal hyperplasia.
Fiet J; Gueux B; Gourmelen M; Kuttenn F; Vexiau P; Couillin P; Pham-Huu-Trung MT; Villette JM; Raux-Demay MC; Galons H
J Clin Endocrinol Metab; 1988 Apr; 66(4):659-67. PubMed ID: 2831244
[TBL] [Abstract][Full Text] [Related]
3. The hypothalamic-pituitary-adrenal axis in partial (late-onset) 21-hydroxylase deficiency.
Feuillan P; Pang S; Schürmeyer T; Avgerinos PC; Chrousos GP
J Clin Endocrinol Metab; 1988 Jul; 67(1):154-60. PubMed ID: 2837498
[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. Pituitary-adrenal responses to corticotropin-releasing hormone in different degrees of adrenal 21-hydroxylase deficiency.
Moreira AC; Elias LL
J Clin Endocrinol Metab; 1992 Jan; 74(1):198-203. PubMed ID: 1309366
[TBL] [Abstract][Full Text] [Related]
6. Usefulness of an ACTH test in the diagnosis of nonclassical 21-hydroxylase deficiency among children presenting with premature pubarche.
Ibáñez L; Bonnin MR; Zampolli M; Prat N; Alia PJ; Navarro MA
Horm Res; 1995; 44(2):51-6. PubMed ID: 7590632
[TBL] [Abstract][Full Text] [Related]
7. Detection of late-onset adrenal hyperplasia in girls with peripubertal virilization.
Sólyom J; Gács G; Keszei K; Láng K; Orley J; Petheö I; Ságodi L
Acta Endocrinol (Copenh); 1987 Jul; 115(3):413-8. PubMed ID: 3039770
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia by simultaneous radioimmunoassay of 21-deoxycortisol and 17-hydroxyprogesterone in amniotic fluid.
Gueux B; Fiet J; Couillin P; Raux-Demay MC; Mornet E; Galons H; Villette JM; Boue J; Dreux C
J Clin Endocrinol Metab; 1988 Mar; 66(3):534-7. PubMed ID: 3258316
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
Winkel CA; Casey ML; Worley RJ; Madden JD; MacDonald PC
J Clin Endocrinol Metab; 1983 Jan; 56(1):104-7. PubMed ID: 6600168
[TBL] [Abstract][Full Text] [Related]
11. Augmented 17 alpha-hydroxyprogesterone response to ACTH stimulation as evidence of decreased 21-hydroxylase activity in patients with incidentally discovered adrenal tumours ('incidentalomas').
Seppel T; Schlaghecke R
Clin Endocrinol (Oxf); 1994 Oct; 41(4):445-51. PubMed ID: 7955456
[TBL] [Abstract][Full Text] [Related]
12. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
Hurwitz A; Brautbar C; Milwidsky A; Vecsei P; Milewicz A; Navot D; Rösler A
J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904
[TBL] [Abstract][Full Text] [Related]
13. Diagnosis of late-onset congenital adrenal hyperplasia in clinical practice: current evaluation.
Sahmay S; Tuten A; Gurleyen H; Oncul M; Benian A; Tamer Erel C
Minerva Endocrinol; 2014 Sep; 39(3):215-22. PubMed ID: 25068307
[TBL] [Abstract][Full Text] [Related]
14. Impaired mineralocorticoid hormone responses to adrenocorticotropin stimulation: additional characterization of heterozygosity for the 21-hydroxylase deficiency type of congenital adrenal hyperplasia.
Pardini DP; Kater CE; Vieira JG; Biglieri EG
J Clin Endocrinol Metab; 1983 Nov; 57(5):1061-6. PubMed ID: 6311859
[TBL] [Abstract][Full Text] [Related]
15. Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.
Speiser PW; New MI
J Clin Endocrinol Metab; 1987 Jan; 64(1):86-91. PubMed ID: 3023431
[TBL] [Abstract][Full Text] [Related]
16. Pituitary-adrenal axis activity in treated congenital adrenal hyperplasia: static and dynamic studies.
Pham-Huu-Trung MT; Gourmelen M; Raux-Eurin MC; Girard F
J Clin Endocrinol Metab; 1978 Aug; 47(2):422-7. PubMed ID: 233672
[TBL] [Abstract][Full Text] [Related]
17. Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension.
de Simone G; Tommaselli AP; Rossi R; Valentino R; Lauria R; Scopacasa F; Lombardi G
Hypertension; 1985; 7(2):204-10. PubMed ID: 2984117
[TBL] [Abstract][Full Text] [Related]
18. The value of low dose (1 microg) ACTH stimulation test in the investigation of non-classic adrenal hyperplasia due to 11beta-hydroxylase deficiency.
Unlühizarci K; Keleştimur F; Güven M; Bayram F; Colak R
Exp Clin Endocrinol Diabetes; 2002 Nov; 110(8):381-5. PubMed ID: 12518247
[TBL] [Abstract][Full Text] [Related]
19. Detection of heterozygous carriers for 21-hydroxylase deficiency by plasma 21-deoxycortisol measurement.
Gourmelen M; Gueux B; Pham Huu Trung MT; Fiet J; Raux-Demay MC; Girard F
Acta Endocrinol (Copenh); 1987 Dec; 116(4):507-12. PubMed ID: 2827419
[TBL] [Abstract][Full Text] [Related]
20. Dexamethasone preparation does not alter corticoid and androgen responses to adrenocorticotropin.
Rosenfield RL; Helke J; Lucky AW
J Clin Endocrinol Metab; 1985 Mar; 60(3):585-9. PubMed ID: 2982902
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
