Similar articles for PMID: 15220035

Year	Number of Results
1987	1
1988	2
1989	1
1990	1
1992	2
1993	2
1994	5
1995	2
1996	4
1997	3
1999	3
2000	2
2001	3
2002	5
2003	1
2004	5
2005	4
2006	8
2007	4
2008	6
2009	5
2010	7
2011	5
2012	5
2013	2
2014	2
2015	2
2016	5
2017	6
2018	2
2019	4
2020	3
2022	2
2024	0

1

Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study.

Arlt W, Walker EA, Draper N, Ivison HE, Ride JP, Hammer F, Chalder SM, Borucka-Mankiewicz M, Hauffa BP, Malunowicz EM, Stewart PM, Shackleton CH. Arlt W, et al. Lancet. 2004 Jun 26;363(9427):2128-35. doi: 10.1016/S0140-6736(04)16503-3. Lancet. 2004. PMID: 15220035

2

Combined homozygous 21 hydroxylase with heterozygous P450 oxidoreductase mutation in a Saudi boy presented with hypertension.

Aljabri A, Alnaim F, Alsaleh Y. Aljabri A, et al. BMJ Case Rep. 2020 Sep 29;13(9):e233942. doi: 10.1136/bcr-2019-233942. BMJ Case Rep. 2020. PMID: 32994263 Free PMC article.

3

P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.

Flück CE, Miller WL. Flück CE, et al. Curr Opin Pediatr. 2006 Aug;18(4):435-41. doi: 10.1097/01.mop.0000236395.71956.5c. Curr Opin Pediatr. 2006. PMID: 16915000 Review.

4

Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.

Krone N, Dhir V, Ivison HE, Arlt W. Krone N, et al. Clin Endocrinol (Oxf). 2007 Feb;66(2):162-72. doi: 10.1111/j.1365-2265.2006.02740.x. Clin Endocrinol (Oxf). 2007. PMID: 17223983 Review.

5

Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interaction.

Riepe FG, Hiort O, Grötzinger J, Sippell WG, Krone N, Holterhus PM. Riepe FG, et al. J Clin Endocrinol Metab. 2008 Jul;93(7):2891-5. doi: 10.1210/jc.2007-2646. Epub 2008 Apr 29. J Clin Endocrinol Metab. 2008. PMID: 18445671

6

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

Patocs A, Liko I, Varga I, Gergics P, Boros A, Futo L, Kun I, Bertalan R, Toth S, Pazmany T, Toth M, Szücs N, Horanyi J, Glaz E, Racz K. Patocs A, et al. J Steroid Biochem Mol Biol. 2005 Nov;97(3):257-65. doi: 10.1016/j.jsbmb.2005.06.035. Epub 2005 Sep 19. J Steroid Biochem Mol Biol. 2005. PMID: 16176874

7

Alternative pathway androgen biosynthesis and human fetal female virilization.

Reisch N, Taylor AE, Nogueira EF, Asby DJ, Dhir V, Berry A, Krone N, Auchus RJ, Shackleton CHL, Hanley NA, Arlt W. Reisch N, et al. Proc Natl Acad Sci U S A. 2019 Oct 29;116(44):22294-22299. doi: 10.1073/pnas.1906623116. Epub 2019 Oct 14. Proc Natl Acad Sci U S A. 2019. PMID: 31611378 Free PMC article.

8

Differential effects of variations in human P450 oxidoreductase on the aromatase activity of CYP19A1 polymorphisms R264C and R264H.

Parween S, DiNardo G, Baj F, Zhang C, Gilardi G, Pandey AV. Parween S, et al. J Steroid Biochem Mol Biol. 2020 Feb;196:105507. doi: 10.1016/j.jsbmb.2019.105507. Epub 2019 Oct 24. J Steroid Biochem Mol Biol. 2020. PMID: 31669572

9

Steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia).

New MI. New MI. Am J Med. 1995 Jan 16;98(1A):2S-8S. doi: 10.1016/s0002-9343(99)80052-7. Am J Med. 1995. PMID: 7825636 Review.

10

Molecular genetics of congenital adrenal hyperplasia.

White PC, New MI. White PC, et al. Baillieres Clin Endocrinol Metab. 1988 Nov;2(4):941-65. doi: 10.1016/s0950-351x(88)80025-9. Baillieres Clin Endocrinol Metab. 1988. PMID: 3077248 Review.

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