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Items: 1 to 20 of 115

1.
2.

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
3.

Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.

Homma K, Hasegawa T, Takeshita E, Watanabe K, Anzo M, Toyoura T, Jinno K, Ohashi T, Hamajima T, Takahashi Y, Takahashi T, Matsuo N.

J Clin Endocrinol Metab. 2004 Dec;89(12):6087-91.

PMID:
15579762
4.

New strategies for detecting steroid metabolic disorders--paneling vs profiling.

Taylor NF, Chan AO.

Clin Chem. 2012 Aug;58(8):1262-3. doi: 10.1373/clinchem.2012.189613. Epub 2012 May 24. No abstract available.

5.

Reduced activity of 11β-hydroxylase accounts for elevated 17α-hydroxyprogesterone in preterms.

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

J Pediatr. 2014 Aug;165(2):280-4. doi: 10.1016/j.jpeds.2014.04.011. Epub 2014 May 23.

PMID:
24862381
6.

Prenatal diagnosis of congenital adrenal hyperplasia caused by P450 oxidoreductase deficiency.

Reisch N, Idkowiak J, Hughes BA, Ivison HE, Abdul-Rahman OA, Hendon LG, Olney AH, Nielsen S, Harrison R, Blair EM, Dhir V, Krone N, Shackleton CH, Arlt W.

J Clin Endocrinol Metab. 2013 Mar;98(3):E528-36. doi: 10.1210/jc.2012-3449. Epub 2013 Jan 30.

7.
8.

Late-onset 21-hydroxylase deficiency: reliable diagnosis by steroid analysis of random urine collections.

Shackleton CH, Irias J, McDonald C, Imperato-McGinley J.

Steroids. 1986 Sep-Oct;48(3-4):239-50.

PMID:
3502202
10.

Diagnosis of 21-hydroxylase deficiency in newborn infants by GC-MS of urinary steroids.

Yong AB, Pitt JJ, Montalto J, Davies HE, Warne GL, Connelly JF.

Aust Paediatr J. 1988 Oct;24(5):280-5.

PMID:
3265870
11.

The diagnosis of 21-hydroxylase deficiency in a prematurely born infant on the basis of the urinary steroid excretion pattern.

van der Ploeg KR, Wolthers BG, Nagel GT, Volmer M, Drayer NM.

Clin Chim Acta. 1982 Apr 23;120(3):341-53.

PMID:
6978779
12.

Cytochrome P450 oxidoreductase deficiency with Antley-Bixler syndrome: steroidogenic capacities.

Iijima S, Ohishi A, Ohzeki T.

J Pediatr Endocrinol Metab. 2009 May;22(5):469-75.

PMID:
19618668
13.
14.

Genetics of congenital adrenal hyperplasia.

Krone N, Arlt W.

Best Pract Res Clin Endocrinol Metab. 2009 Apr;23(2):181-92. doi: 10.1016/j.beem.2008.10.014. Review.

PMID:
19500762
15.

Capillary gas chromatography as a tool for characterization of urinary steroid excretion in patients with congenital adrenal hyperplasia.

Vierhapper H, Nowotny P, Waldhäusl W, Frisch H.

J Steroid Biochem. 1985 Mar;22(3):363-9.

PMID:
3990286
17.

17-Hydroxylase/C17,20-lyase (CYP17) is not the enzyme responsible for side-chain cleavage of cortisol and its metabolites.

Shackleton CH, Neres MS, Hughes BA, Stewart PM, Kater CE.

Steroids. 2008 Jul;73(6):652-6. doi: 10.1016/j.steroids.2008.02.001. Epub 2008 Feb 13.

PMID:
18355883
18.

Transient hyper-17-OHPnemia unrelated to cross-reactions with residual fetal adrenal cortex products.

Mizuno H, Ohro Y, Sugiyama Y, Ito T, Hasegawa T, Homma K, Ueshiba H, Ono M, Togari H.

Horm Res. 2004;61(5):242-5. Epub 2004 Feb 26.

PMID:
14988602
20.

Steroids excreted in urine by neonates with 21-hydroxylase deficiency: characterization, using GC-MS and GC-MS/MS, of the D-ring and side chain structure of pregnanes and pregnenes.

Christakoudi S, Cowan DA, Taylor NF.

Steroids. 2010 Jan;75(1):34-52. doi: 10.1016/j.steroids.2009.09.011. Epub 2009 Sep 30.

PMID:
19799922
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