126 related articles for article (PubMed ID: 2152934)
1. Adrenal steroidogenic function in a black and Hispanic population with precocious pubarche.
Oberfield SE; Mayes DM; Levine LS
J Clin Endocrinol Metab; 1990 Jan; 70(1):76-82. PubMed ID: 2152934
[TBL] [Abstract][Full Text] [Related]
2. Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels.
Sakkal-Alkaddour H; Zhang L; Yang X; Chang YT; Kappy M; Slover RS; Jorgensen V; Pang S
J Clin Endocrinol Metab; 1996 Nov; 81(11):3961-5. PubMed ID: 8923844
[TBL] [Abstract][Full Text] [Related]
3. Newly proposed hormonal criteria via genotypic proof for type II 3beta-hydroxysteroid dehydrogenase deficiency.
Lutfallah C; Wang W; Mason JI; Chang YT; Haider A; Rich B; Castro-Magana M; Copeland KC; David R; Pang S
J Clin Endocrinol Metab; 2002 Jun; 87(6):2611-22. PubMed ID: 12050224
[TBL] [Abstract][Full Text] [Related]
4. Genetic defects of steroidogenesis in premature pubarche.
Temeck JW; Pang SY; Nelson C; New MI
J Clin Endocrinol Metab; 1987 Mar; 64(3):609-17. PubMed ID: 3029158
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Adrenal steroidogenic defects in children with precocious pubarche.
del Balzo P; Borrelli P; Cambiaso P; Danielli E; Cappa M
Horm Res; 1992; 37(4-5):180-4. PubMed ID: 1337057
[TBL] [Abstract][Full Text] [Related]
7. Serum and urinary steroids in girls with precocious pubarche and/or hirsutism due to mild 3-beta-hydroxysteroid dehydrogenase deficiency.
Sólyom J; Halász Z; Hosszú E; Gláz E; Vihko R; Orava M; Homoki J; Wudy SA; Teller WM
Horm Res; 1995; 44(3):133-41. PubMed ID: 7590644
[TBL] [Abstract][Full Text] [Related]
8. Late-onset adrenal steroid 3 beta-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women.
Pang SY; Lerner AJ; Stoner E; Levine LS; Oberfield SE; Engel I; New MI
J Clin Endocrinol Metab; 1985 Mar; 60(3):428-39. PubMed ID: 2982896
[TBL] [Abstract][Full Text] [Related]
9. Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
Mermejo LM; Elias LL; Marui S; Moreira AC; Mendonca BB; de Castro M
J Clin Endocrinol Metab; 2005 Mar; 90(3):1287-93. PubMed ID: 15585552
[TBL] [Abstract][Full Text] [Related]
10. Absence of nonclassical congenital adrenal hyperplasia in patients with precocious adrenarche.
Morris AH; Reiter EO; Geffner ME; Lippe BM; Itami RM; Mayes DM
J Clin Endocrinol Metab; 1989 Oct; 69(4):709-15. PubMed ID: 2550505
[TBL] [Abstract][Full Text] [Related]
11. Ovarian steroidogenic responses to gonadotropin-releasing hormone agonist testing with nafarelin in hirsute women with adrenal responses to adrenocorticotropin suggestive of 3 beta-hydroxy-delta 5-steroid dehydrogenase deficiency.
Barnes RB; Ehrmann DA; Brigell DF; Rosenfield RL
J Clin Endocrinol Metab; 1993 Feb; 76(2):450-5. PubMed ID: 8381802
[TBL] [Abstract][Full Text] [Related]
12. Identification of nonclassical 21-hydroxylase deficiency in girls with precocious pubarche.
Leite MV; Mendonça BB; Arnhold IJ; Estefan V; Nunes C; Nicolau W; Bloise W
J Endocrinol Invest; 1991 Jan; 14(1):11-5. PubMed ID: 1646249
[TBL] [Abstract][Full Text] [Related]
13. Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test.
Pang S; Carbunaru G; Haider A; Copeland KC; Chang YT; Lutfallah C; Mason JI
Clin Endocrinol (Oxf); 2003 Mar; 58(3):323-31. PubMed ID: 12608938
[TBL] [Abstract][Full Text] [Related]
14. Mild adrenal 3 beta-hydroxysteroid dehydrogenase deficiency in children with accelerated growth, premature pubarche and/or hirsutism.
Nishi Y; Tezuka T
Eur J Pediatr; 1992 Jan; 151(1):19-23. PubMed ID: 1309452
[TBL] [Abstract][Full Text] [Related]
15. The roles of insulin sensitivity, insulin-like growth factor I (IGF-I), and IGF-binding protein-1 and -3 in the hyperandrogenism of African-American and Caribbean Hispanic girls with premature adrenarche.
Vuguin P; Linder B; Rosenfeld RG; Saenger P; DiMartino-Nardi J
J Clin Endocrinol Metab; 1999 Jun; 84(6):2037-42. PubMed ID: 10372707
[TBL] [Abstract][Full Text] [Related]
16. 3 alpha-Androstanediol glucuronide in premature and normal pubarche.
Riddick LM; Garibaldi LR; Wang ME; Senne AR; Klimah PE; Clark AT; Levine LS; Oberfield SE; Pang SY
J Clin Endocrinol Metab; 1991 Jan; 72(1):46-50. PubMed ID: 1846006
[TBL] [Abstract][Full Text] [Related]
17. Absence of molecular defect in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3 beta-HSD activity.
Chang YT; Zhang L; Alkaddour HS; Mason JI; Lin K; Yang X; Garibaldi LR; Bourdony CJ; Dolan LM; Donaldson DL
Pediatr Res; 1995 Jun; 37(6):820-4. PubMed ID: 7651769
[TBL] [Abstract][Full Text] [Related]
18. Excess weight and precocious pubarche in children: alterations of the adrenocortical hormones.
Jabbar M; Pugliese M; Fort P; Recker B; Lifshitz F
J Am Coll Nutr; 1991 Aug; 10(4):289-96. PubMed ID: 1654353
[TBL] [Abstract][Full Text] [Related]
19. Girls diagnosed with premature pubarche show an exaggerated ovarian androgen synthesis from the early stages of puberty: evidence from gonadotropin-releasing hormone agonist testing.
Ibáñez L; Potau N; Zampolli M; Street ME; Carrascosa A
Fertil Steril; 1997 May; 67(5):849-55. PubMed ID: 9130889
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]