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.
207 related articles for article (PubMed ID: 18574213)
1. Congenital adrenal hyperplasia in adolescents: diagnosis and management. Lin-Su K; Nimkarn S; New MI Ann N Y Acad Sci; 2008; 1135():95-8. PubMed ID: 18574213 [TBL] [Abstract][Full Text] [Related]
2. Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment. Carlson AD; Obeid JS; Kanellopoulou N; Wilson RC; New MI J Steroid Biochem Mol Biol; 1999; 69(1-6):19-29. PubMed ID: 10418977 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the pre-screening era. Lee CT; Tung YC; Hsiao PH; Lee JS; Tsai WY J Formos Med Assoc; 2010 Feb; 109(2):148-55. PubMed ID: 20206839 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene. Moura-Massari VO; Cunha FS; Gomes LG; Bugano Diniz Gomes D; Marcondes JA; Madureira G; de Mendonca BB; Bachega TA PLoS One; 2016; 11(2):e0148548. PubMed ID: 26848581 [TBL] [Abstract][Full Text] [Related]
8. Rare mutations in the CYP21A2 gene detected in congenital adrenal hyperplasia. Neocleous V; Ioannou YS; Bartsota M; Costi C; Skordis N; Phylactou LA Clin Biochem; 2009 Sep; 42(13-14):1363-7. PubMed ID: 19501079 [TBL] [Abstract][Full Text] [Related]
9. [Detection of CYP21A2 gene mutations and the differences in the levels of hormones in patients with 21-hydroxylase deficiency]. Gao YJ; Yu BQ; Lu L; Wu XY; Mao JF; Wang X; Tong AL; Chen S; Nie M Zhonghua Yi Xue Za Zhi; 2020 Mar; 100(8):586-592. PubMed ID: 32164112 [No Abstract] [Full Text] [Related]
10. CYP21A2 genotypes do not predict the severity of hyperandrogenic manifestations in the nonclassical form of congenital adrenal hyperplasia. Moura-Massari VO; Bugano DD; Marcondes JA; Gomes LG; Mendonca BB; Bachega TA Horm Metab Res; 2013 Apr; 45(4):301-7. PubMed ID: 23322511 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification. Theodoropoulou M; Barta C; Szoke M; Guttman A; Staub M; Niederland T; Sólyom J; Fekete G; Sasvari-Szekely M Fetal Diagn Ther; 2001; 16(4):237-40. PubMed ID: 11399887 [TBL] [Abstract][Full Text] [Related]
12. Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Bidet M; Bellanné-Chantelot C; Galand-Portier MB; Golmard JL; Tardy V; Morel Y; Clauin S; Coussieu C; Boudou P; Mowzowicz I; Bachelot A; Touraine P; Kuttenn F J Clin Endocrinol Metab; 2010 Mar; 95(3):1182-90. PubMed ID: 20080854 [TBL] [Abstract][Full Text] [Related]