Krone N - Search Results

1

Functional characterization of three CYP21A2 sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system.

Bleicken C, Loidi L, Dhir V, Parajes S, Quinteiro C, Dominguez F, Grötzinger J, Sippell WG, Riepe FG, Arlt W, Krone N. Bleicken C, et al. Among authors: krone n. Hum Mutat. 2009 Feb;30(2):E443-50. doi: 10.1002/humu.20926. Hum Mutat. 2009. PMID: 19058224

2

Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia.

Krone N, Braun A, Weinert S, Peter M, Roscher AA, Partsch CJ, Sippell WG. Krone N, et al. Clin Chem. 2002 Jun;48(6 Pt 1):818-25. Clin Chem. 2002. PMID: 12028996

3

Management of congenital adrenal hyperplasia: results of the ESPE questionnaire.

Riepe FG, Krone N, Viemann M, Partsch CJ, Sippell WG. Riepe FG, et al. Among authors: krone n. Horm Res. 2002;58(4):196-205. doi: 10.1159/000065492. Horm Res. 2002. PMID: 12324719

4

Chromatographic system for the simultaneous measurement of plasma 18-hydroxy-11-deoxycorticosterone and 18-hydroxycorticosterone by radioimmunoassay: reference data for neonates and infants and its application in aldosterone-synthase deficiency.

Riepe FG, Krone N, Peter M, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: krone n. J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Mar 5;785(2):293-301. doi: 10.1016/s1570-0232(02)00921-2. J Chromatogr B Analyt Technol Biomed Life Sci. 2003. PMID: 12554142

5

Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneity.

Riepe FG, Krone N, Morlot M, Ludwig M, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: krone n. J Clin Endocrinol Metab. 2003 Apr;88(4):1683-6. doi: 10.1210/jc.2002-021556. J Clin Endocrinol Metab. 2003. PMID: 12679457

6

Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene.

Riepe FG, Krone N, Morlot M, Peter M, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: krone n. J Clin Endocrinol Metab. 2004 May;89(5):2150-2. doi: 10.1210/jc.2003-031555. J Clin Endocrinol Metab. 2004. PMID: 15126534

7

Congenital adrenal hyperplasia - how to improve the transition from adolescence to adult life.

Kruse B, Riepe FG, Krone N, Bosinski HA, Kloehn S, Partsch CJ, Sippell WG, Mönig H. Kruse B, et al. Among authors: krone n. Exp Clin Endocrinol Diabetes. 2004 Jul;112(7):343-55. doi: 10.1055/s-2004-821013. Exp Clin Endocrinol Diabetes. 2004. PMID: 15239019 Review.

8

Treatment of pubertal gynecomastia with the specific aromatase inhibitor anastrozole.

Riepe FG, Baus I, Wiest S, Krone N, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: krone n. Horm Res. 2004;62(3):113-8. doi: 10.1159/000079882. Epub 2004 Jul 20. Horm Res. 2004. PMID: 15273427 Clinical Trial.

9

Long-term follow-up of spontaneous development in a boy with familial male precocious puberty.

Partsch CJ, Krone N, Riepe FG, Gromoll J, Sippell WG. Partsch CJ, et al. Among authors: krone n. Horm Res. 2004;62(4):177-81. doi: 10.1159/000080887. Epub 2004 Sep 15. Horm Res. 2004. PMID: 15375328

10

Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Krone N, Riepe FG, Grötzinger J, Partsch CJ, Sippell WG. Krone N, et al. J Clin Endocrinol Metab. 2005 Jan;90(1):445-54. doi: 10.1210/jc.2004-0813. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483094

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