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Items: 1 to 20 of 63

1.

High incidence of molecular defects of the CYP21 gene in patients with premature adrenarche.

Dacou-Voutetakis C, Dracopoulou M.

J Clin Endocrinol Metab. 1999 May;84(5):1570-4.

PMID:
10323382
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.

PMID:
9666866
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.

PMID:
8045980
4.

Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency.

Speiser PW, New MI.

J Clin Endocrinol Metab. 1987 Jan;64(1):86-91.

PMID:
3023431
5.

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.

PMID:
2550505
6.

Hyperandrogenism and manifesting heterozygotes for 21-hydroxylase deficiency.

Witchel SF, Lee PA, Suda-Hartman M, Hoffman EP.

Biochem Mol Med. 1997 Dec;62(2):151-8.

PMID:
9441866
7.

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.

PMID:
2982895
8.

Molecular defects of the CYP21 gene in Spanish girls with isolated precocious pubarche.

Potau N, Riqué S, Eduardo I, Marcos V, Ibañez L.

Eur J Endocrinol. 2002 Oct;147(4):485-8.

9.

'Exaggerated adrenarche' in children presenting with premature adrenarche.

Likitmaskul S, Cowell CT, Donaghue K, Kreutzmann DJ, Howard NJ, Blades B, Silink M.

Clin Endocrinol (Oxf). 1995 Mar;42(3):265-72.

PMID:
7758231
10.

Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women.

Blanché H, Vexiau P, Clauin S, Le Gall I, Fiet J, Mornet E, Dausset J, Bellanné-Chantelot C.

Hum Genet. 1997 Nov;101(1):56-60.

PMID:
9385370
11.

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.

PMID:
8923844
12.

Altered sensitivity to low dose dexamethasone in a subset of patients with premature adrenarche.

Oberfield SE, Amer T, Tyson D, Soranno D, David R, Lee E, Levine LS.

J Clin Endocrinol Metab. 1994 Oct;79(4):1102-4.

PMID:
7962281
13.

ACTH receptor promoter polymorphism associates with severity of premature adrenarche and modulates hypothalamo-pituitary-adrenal axis in children.

Lappalainen S, Utriainen P, Kuulasmaa T, Voutilainen R, Jääskeläinen J.

Pediatr Res. 2008 Apr;63(4):410-4. doi: 10.1203/PDR.0b013e3181659c14.

PMID:
18356748
14.

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.

PMID:
3029158
15.

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.

PMID:
3022523
16.

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.

PMID:
9579234
17.

Changes in steroid pattern following acute and chronic adrenocorticotropin administration in premature adrenarche.

Toscano V, Balducci R, Adamo MV, Mangiantini A, Cives C, Boscherini B.

J Steroid Biochem. 1989 Feb;32(2):321-6.

PMID:
2537914
18.

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. Epub 2004 Dec 7.

PMID:
15585552
19.

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.

PMID:
22308849
20.

Prepubertal acne: a cutaneous marker of androgen excess?

De Raeve L, De Schepper J, Smitz J.

J Am Acad Dermatol. 1995 Feb;32(2 Pt 1):181-4.

PMID:
7829699

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