305 related articles for article (PubMed ID: 9666866)
1. 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]
2. 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]
3. 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]
4. Is heterozygosity for the steroid 21-hydroxylase deficiency responsible for hirsutism, premature pubarche, early puberty, and precocious puberty in children?
Knorr D; Bidlingmaier F; Höller W; Kuhnle U; Meiler B; Nachmann A
Acta Endocrinol Suppl (Copenh); 1986; 279():284-9. PubMed ID: 3022523
[TBL] [Abstract][Full Text] [Related]
5. Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency.
Weintrob N; Brautbar C; Pertzelan A; Josefsberg Z; Dickerman Z; Kauschansky A; Lilos P; Peled D; Phillip M; Israel S
Eur J Endocrinol; 2000 Sep; 143(3):397-403. PubMed ID: 11022183
[TBL] [Abstract][Full Text] [Related]
6. Early polycystic ovary-like syndrome in girls with central precocious puberty and exaggerated adrenal response.
Lazar L; Kauli R; Bruchis C; Nordenberg J; Galatzer A; Pertzelan A
Eur J Endocrinol; 1995 Oct; 133(4):403-6. PubMed ID: 7581961
[TBL] [Abstract][Full Text] [Related]
7. Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche.
Savas Erdeve S; Berberoglu M; Yurur-Kutlay N; Siklar Z; Hacihamdioglu B; Tukun A; Ocal G
J Pediatr Endocrinol Metab; 2011; 24(11-12):965-70. PubMed ID: 22308849
[TBL] [Abstract][Full Text] [Related]
8. Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche.
Ghizzoni L; Cappa M; Vottero A; Ubertini G; Carta D; Di Iorgi N; Gasco V; Marchesi M; Raggi V; Ibba A; Napoli F; Massimi A; Maghnie M; Loche S; Porzio O
Eur J Endocrinol; 2011 Aug; 165(2):307-14. PubMed ID: 21646284
[TBL] [Abstract][Full Text] [Related]
9. 17-Hydroxyprogesterone in children, adolescents and adults.
Honour JW
Ann Clin Biochem; 2014 Jul; 51(Pt 4):424-40. PubMed ID: 24711560
[TBL] [Abstract][Full Text] [Related]
10. 21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease.
Forest MG; Tardy V; Nicolino M; David M; Morel Y
Ann Endocrinol (Paris); 2005 Jun; 66(3):225-32. PubMed ID: 15988383
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
Speiser PW; New MI; White PC
N Engl J Med; 1988 Jul; 319(1):19-23. PubMed ID: 3260007
[TBL] [Abstract][Full Text] [Related]
13. Molecular analysis of CYP21 gene mutations carried on HLA-B14 positive haplotypes.
Dondi E; Cuccia M; Keller E; Martinetti M; Larizza D; Albert ED
Eur J Immunogenet; 1994 Oct; 21(5):341-50. PubMed ID: 9098443
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Carrier status for steroid 21-hydroxylase deficiency is only one factor in the variable phenotype of acne.
Ostlere LS; Rumsby G; Holownia P; Jacobs HS; Rustin MH; Honour JW
Clin Endocrinol (Oxf); 1998 Feb; 48(2):209-15. PubMed ID: 9579234
[TBL] [Abstract][Full Text] [Related]
16. 17-Hydroxyprogesterone responses to adrenocorticotropin in children with premature adrenarche.
Granoff AB; Chasalow FI; Blethen SL
J Clin Endocrinol Metab; 1985 Mar; 60(3):409-15. PubMed ID: 2982895
[TBL] [Abstract][Full Text] [Related]
17. High prevalence of abnormal adrenal response in girls with central precocious puberty at early pubertal stages.
Lazar L; Kauli R; Bruchis C; Nordenberg J; Galatzer A; Pertzelan A
Eur J Endocrinol; 1995 Oct; 133(4):407-11. PubMed ID: 7581962
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Anthropometric and endocrine features in girls with isolated premature pubarche or non-classical congenital adrenal hyperplasia.
Accetta SG; Di Domênico K; Ritter CG; Ritter AT; Capp E; Spritzer PM
J Pediatr Endocrinol Metab; 2004 May; 17(5):767-73. PubMed ID: 15237712
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]