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Items: 1 to 20 of 120

1.

Androgen synthesis in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Kamrath C, Hartmann MF, Wudy SA.

Horm Metab Res. 2013 Feb;45(2):86-91. doi: 10.1055/s-0032-1331751. Epub 2013 Jan 23. Review.

PMID:
23345132
2.

The activities of 5α-reductase and 17,20-lyase determine the direction through androgen synthesis pathways in patients with 21-hydroxylase deficiency.

Kamrath C, Hartmann MF, Remer T, Wudy SA.

Steroids. 2012 Nov;77(13):1391-7. doi: 10.1016/j.steroids.2012.08.001. Epub 2012 Aug 23.

PMID:
22951291
3.

Increased activation of the alternative "backdoor" pathway in patients with 21-hydroxylase deficiency: evidence from urinary steroid hormone analysis.

Kamrath C, Hochberg Z, Hartmann MF, Remer T, Wudy SA.

J Clin Endocrinol Metab. 2012 Mar;97(3):E367-75. doi: 10.1210/jc.2011-1997. Epub 2011 Dec 14.

PMID:
22170725
4.

[The alternative androgen synthesis pathway in humans].

Kamrath C, Hartmann MF, Wudy S.

Klin Padiatr. 2013 Jan;225(1):3-7. doi: 10.1055/s-0032-1331170. Epub 2013 Jan 17. Review. German.

PMID:
23329621
5.

Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: implication for the backdoor pathway to dihydrotestosterone.

Homma K, Hasegawa T, Nagai T, Adachi M, Horikawa R, Fujiwara I, Tajima T, Takeda R, Fukami M, Ogata T.

J Clin Endocrinol Metab. 2006 Jul;91(7):2643-9. Epub 2006 Apr 11.

PMID:
16608896
6.

Modified-Release and Conventional Glucocorticoids and Diurnal Androgen Excretion in Congenital Adrenal Hyperplasia.

Jones CM, Mallappa A, Reisch N, Nikolaou N, Krone N, Hughes BA, O'Neil DM, Whitaker MJ, Tomlinson JW, Storbeck KH, Merke DP, Ross RJ, Arlt W.

J Clin Endocrinol Metab. 2017 Jun 1;102(6):1797-1806. doi: 10.1210/jc.2016-2855.

PMID:
27845856
7.

New insights into steroidogenesis in normo- and hyperandrogenic polycystic ovary syndrome patients.

Medeiros SF, Gil-Junior AB, Barbosa JS, Isaías ED, Yamamoto MM.

Arq Bras Endocrinol Metabol. 2013 Aug;57(6):437-44.

8.

Adrenal androgen hyperresponsiveness to adrenocorticotropin in women with acne and/or hirsutism: adrenal enzyme defects and exaggerated adrenarche.

Lucky AW, Rosenfield RL, McGuire J, Rudy S, Helke J.

J Clin Endocrinol Metab. 1986 May;62(5):840-8.

PMID:
3007557
9.

Androgen biosynthesis during minipuberty favors the backdoor pathway over the classic pathway: Insights into enzyme activities and steroid fluxes in healthy infants during the first year of life from the urinary steroid metabolome.

Dhayat NA, Dick B, Frey BM, d'Uscio CH, Vogt B, Flück CE.

J Steroid Biochem Mol Biol. 2017 Jan;165(Pt B):312-322. doi: 10.1016/j.jsbmb.2016.07.009. Epub 2016 Jul 25.

PMID:
27471148
10.

Late-onset congenital adrenal hyperplasia in women with hirsutism.

Arnaout MA.

Eur J Clin Invest. 1992 Oct;22(10):651-8.

PMID:
1333959
11.

'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
12.

Assessment of the potential of polyphenols as a CYP17 inhibitor free of adverse corticosteroid elevation.

Lin CJ, Cheng LC, Lin TC, Wang CJ, Li LA.

Biochem Pharmacol. 2014 Aug 1;90(3):288-96. doi: 10.1016/j.bcp.2014.05.013. Epub 2014 May 27.

PMID:
24875446
13.

Androglottia in a young female adolescent with congenital adrenal hyperplasia and 21-hydroxylase deficiency.

Fürst-Recktenwald S, Dörr HG, Rosanowski F.

J Pediatr Endocrinol Metab. 2000 Jul-Aug;13(7):959-62.

PMID:
10968487
14.

On the origin of the elevated 17-hydroxyprogesterone levels after adrenal stimulation in hyperandrogenism.

Azziz R, Rafi A, Smith BR, Bradley EL Jr, Zacur HA.

J Clin Endocrinol Metab. 1990 Feb;70(2):431-6.

PMID:
2137133
15.

Clinical implications of androgen synthesis via 5alpha-reduced precursors.

Ghayee HK, Auchus RJ.

Endocr Dev. 2008;13:55-66. doi: 10.1159/000134780. Review.

PMID:
18493133
16.

[Comparative characteristics of steroidogenesis and its biorhythm in the hyperfunctioning adrenal cortex].

Kolesnikova GS, Goncharov NP, Vorontsov VI, Marova EI, Rozhinskaia LIa.

Vestn Ross Akad Med Nauk. 1994;(12):39-44. Russian.

PMID:
7742657
17.

The urinary steroidome of treated children with classic 21-hydroxylase deficiency.

Kamrath C, Wettstaedt L, Boettcher C, Hartmann MF, Wudy SA.

J Steroid Biochem Mol Biol. 2017 Jan;165(Pt B):396-406. doi: 10.1016/j.jsbmb.2016.08.006. Epub 2016 Aug 17.

PMID:
27544322
18.

Menstrual disturbance and hypersecretion of progesterone in women with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Holmes-Walker DJ, Conway GS, Honour JW, Rumsby G, Jacobs HS.

Clin Endocrinol (Oxf). 1995 Sep;43(3):291-6.

PMID:
7586597
19.

The 17, 20-lyase activity of cytochrome p450c17 from human fetal testis favors the delta5 steroidogenic pathway.

Flück CE, Miller WL, Auchus RJ.

J Clin Endocrinol Metab. 2003 Aug;88(8):3762-6.

PMID:
12915666
20.

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