These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
543 related articles for article (PubMed ID: 8306479)
1. Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families. Larizza D; Cuccia M; Martinetti M; Maghnie M; Dondi E; Salvaneschi L; Severi F Clin Endocrinol (Oxf); 1994 Jan; 40(1):39-45. PubMed ID: 8306479 [TBL] [Abstract][Full Text] [Related]
2. Exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation and evidence for CYP21B gene point mutations in true precocious puberty. Cisternino M; Dondi E; Martinetti M; Lorini R; Salvaneschi L; Cuccia M; Severi F Clin Endocrinol (Oxf); 1998 May; 48(5):555-60. PubMed ID: 9666866 [TBL] [Abstract][Full Text] [Related]
3. Autoimmunity, HLA, Gm and Km polymorphisms in Turner's syndrome. Larizza D; Martinetti Bianchi M; Lorini R; Maghnie M; Dugoujon JM; Cuccia Belvedere M; Severi F Autoimmunity; 1989; 4(1-2):69-78. PubMed ID: 2491644 [TBL] [Abstract][Full Text] [Related]
4. Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome. Onder A; Aycan Z; Cetinkaya S; Kendirci HN; Bas VN; Agladioglu SY J Pediatr Endocrinol Metab; 2012; 25(7-8):681-5. PubMed ID: 23155693 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Screening for non-classic 21-hydroxylase deficiency in an HLA-B14 positive population. Motta P; Airaghi L; Catania A; Mangone I; Orsatti A; Tenconi L; Cantalamessa L; Zanussi C Acta Endocrinol (Copenh); 1987 Oct; 116(2):211-5. PubMed ID: 2821719 [TBL] [Abstract][Full Text] [Related]
7. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype. Libber SM; Migeon CJ; Bias WB J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788 [TBL] [Abstract][Full Text] [Related]
8. Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms. Balsamo A; Revelli A; Borelli I; Amoroso A; Cenderelli G; De Sanso G; Mazzola G; Curtoni ES; Zoppetti G; Massobrio M Gynecol Endocrinol; 1992 Jun; 6(2):91-8. PubMed ID: 1354409 [TBL] [Abstract][Full Text] [Related]
9. Isolated precocious pubarche: an approach. Balducci R; Boscherini B; Mangiantini A; Morellini M; Toscano V J Clin Endocrinol Metab; 1994 Aug; 79(2):582-9. PubMed ID: 8045980 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 'Cryptic' form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in the Yugoslav population. Dumić M; Brkljacić L; Mardesić D; Plavsić V; Lukenda M; Kastelan A Acta Endocrinol (Copenh); 1985 Jul; 109(3):386-92. PubMed ID: 2992207 [TBL] [Abstract][Full Text] [Related]
12. Parental GM and HLA genotypes and reduced birth weight in patients with Turner's syndrome. Larizza D; Martinetti M; Dugoujon JM; Tinelli C; Calcaterra V; Cuccia M; Salvaneschi L; Severi F J Pediatr Endocrinol Metab; 2002; 15(8):1183-90. PubMed ID: 12387517 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Limited value of serum steroid measurements in identification of mild form of 21-hydroxylase deficiency. Török D; Halász Z; Garami M; Homoki J; Fekete G; Sólyom J Exp Clin Endocrinol Diabetes; 2003 Feb; 111(1):27-32. PubMed ID: 12605347 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Screening heterozygotes for 21-hydroxylase deficiency among hirsute women: lack of utility of the adrenocorticotropin hormone test. Dewailly D; Vantyghem MC; Lemaire C; Dufosse F; Racadot A; Fossati P Fertil Steril; 1988 Aug; 50(2):228-32. PubMed ID: 2840308 [TBL] [Abstract][Full Text] [Related]
17. Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status. Dolzan V; Prezelj J; Vidan-Jeras B; Breskvar K Eur J Endocrinol; 1999 Aug; 141(2):132-9. PubMed ID: 10427156 [TBL] [Abstract][Full Text] [Related]
18. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency. Levine LS; Dupont B; Lorenzen F; Pang S; Pollack M; Oberfield SE; Kohn B; Lerner A; Cacciari E; Mantero F; Cassio A; Scaroni C; Chiumello G; Rondanini GF; Gargantini L; Giovannelli G; Virdis R; Bartolotta E; Migliori C; Pintor C; Tato L; Barboni F; New MI J Clin Endocrinol Metab; 1981 Dec; 53(6):1193-8. PubMed ID: 6271801 [TBL] [Abstract][Full Text] [Related]
19. [Determination of urinary 17 alpha-hydroxyprogesterone excretion using ELISA--evaluation of normal subjects and patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. Shibata Y Nihon Naibunpi Gakkai Zasshi; 1991 Aug; 67(8):819-39. PubMed ID: 1813324 [TBL] [Abstract][Full Text] [Related]
20. Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome. Atabek ME; Kurtoğlu S; Keskin M Turk J Pediatr; 2005; 47(2):176-9. PubMed ID: 16052861 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]