Krone N - Search Results

1

Novel associations in disorders of sex development: findings from the I-DSD Registry.

Cox K, Bryce J, Jiang J, Rodie M, Sinnott R, Alkhawari M, Arlt W, Audi L, Balsamo A, Bertelloni S, Cools M, Darendeliler F, Drop S, Ellaithi M, Guran T, Hiort O, Holterhus PM, Hughes I, Krone N, Lisa L, Morel Y, Soder O, Wieacker P, Ahmed SF. Cox K, et al. Among authors: krone n. J Clin Endocrinol Metab. 2014 Feb;99(2):E348-55. doi: 10.1210/jc.2013-2918. Epub 2013 Dec 3. J Clin Endocrinol Metab. 2014. PMID: 24302751 Free PMC article.

2

Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.

Riepe FG, Ahrens W, Krone N, Fölster-Holst R, Brasch J, Sippell WG, Hiort O, Partsch CJ. Riepe FG, et al. Among authors: krone n. Eur J Endocrinol. 2005 Apr;152(4):515-9. doi: 10.1530/eje.1.01879. Eur J Endocrinol. 2005. PMID: 15817905

3

Thirteen novel mutations in the NR0B1 (DAX1) gene as cause of adrenal hypoplasia congenita.

Krone N, Riepe FG, Dörr HG, Morlot M, Rudorff KH, Drop SL, Weigel J, Pura M, Kreze A, Boronat M, de Luca F, Tiulpakov A, Partsch CJ, Peter M, Sippell WG. Krone N, et al. Hum Mutat. 2005 May;25(5):502-3. doi: 10.1002/humu.9331. Hum Mutat. 2005. PMID: 15841486

4

Analyzing the functional and structural consequences of two point mutations (P94L and A368D) in the CYP11B1 gene causing congenital adrenal hyperplasia resulting from 11-hydroxylase deficiency.

Krone N, Grischuk Y, Müller M, Volk RE, Grötzinger J, Holterhus PM, Sippell WG, Riepe FG. Krone N, et al. J Clin Endocrinol Metab. 2006 Jul;91(7):2682-8. doi: 10.1210/jc.2006-0209. Epub 2006 May 2. J Clin Endocrinol Metab. 2006. PMID: 16670167

5

Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1.

Riepe FG, Finkeldei J, de Sanctis L, Einaudi S, Testa A, Karges B, Peter M, Viemann M, Grötzinger J, Sippell WG, Fejes-Toth G, Krone N. Riepe FG, et al. Among authors: krone n. J Clin Endocrinol Metab. 2006 Nov;91(11):4552-61. doi: 10.1210/jc.2006-1161. Epub 2006 Sep 5. J Clin Endocrinol Metab. 2006. PMID: 16954160

6

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.

7

Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287P.

Dhir V, Ivison HE, Krone N, Shackleton CH, Doherty AJ, Stewart PM, Arlt W. Dhir V, et al. Among authors: krone n. Mol Endocrinol. 2007 Aug;21(8):1958-68. doi: 10.1210/me.2007-0066. Epub 2007 May 15. Mol Endocrinol. 2007. PMID: 17505056

8

Age-specific changes in sex steroid biosynthesis and sex development.

Krone N, Hanley NA, Arlt W. Krone N, et al. Best Pract Res Clin Endocrinol Metab. 2007 Sep;21(3):393-401. doi: 10.1016/j.beem.2007.06.001. Best Pract Res Clin Endocrinol Metab. 2007. PMID: 17875487 Review.

9

Adult consequences of congenital adrenal hyperplasia.

Arlt W, Krone N. Arlt W, et al. Among authors: krone n. Horm Res. 2007;68 Suppl 5:158-64. doi: 10.1159/000110615. Epub 2007 Dec 10. Horm Res. 2007. PMID: 18174737 Review.

10

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. Among authors: krone n. 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

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