Krone N - Search Results

1

Health status of adults with congenital adrenal hyperplasia: a cohort study of 203 patients.

Arlt W, Willis DS, Wild SH, Krone N, Doherty EJ, Hahner S, Han TS, Carroll PV, Conway GS, Rees DA, Stimson RH, Walker BR, Connell JM, Ross RJ; United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE). Arlt W, et al. Among authors: krone n. J Clin Endocrinol Metab. 2010 Nov;95(11):5110-21. doi: 10.1210/jc.2010-0917. Epub 2010 Aug 18. J Clin Endocrinol Metab. 2010. PMID: 20719839 Free PMC article.

2

Mothers with congenital adrenal hyperplasia and their children: outcome of pregnancy, birth and childhood.

Krone N, Wachter I, Stefanidou M, Roscher AA, Schwarz HP. Krone N, et al. Clin Endocrinol (Oxf). 2001 Oct;55(4):523-9. doi: 10.1046/j.1365-2265.2001.01359.x. Clin Endocrinol (Oxf). 2001. PMID: 11678836

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

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.

5

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

6

Congenital adrenal hyperplasia: the molecular basis of 21-hydroxylase deficiency in H-2(aw18) mice.

Riepe FG, Tatzel S, Sippell WG, Pleiss J, Krone N. Riepe FG, et al. Among authors: krone n. Endocrinology. 2005 Jun;146(6):2563-74. doi: 10.1210/en.2004-1563. Epub 2005 Feb 24. Endocrinology. 2005. PMID: 15731361

7

Congenital adrenal hyperplasia due to 11-hydroxylase deficiency: functional characterization of two novel point mutations and a three-base pair deletion in the CYP11B1 gene.

Krone N, Riepe FG, Götze D, Korsch E, Rister M, Commentz J, Partsch CJ, Grötzinger J, Peter M, Sippell WG. Krone N, et al. J Clin Endocrinol Metab. 2005 Jun;90(6):3724-30. doi: 10.1210/jc.2005-0089. Epub 2005 Mar 8. J Clin Endocrinol Metab. 2005. PMID: 15755848

8

Absence of exercise-induced leptin suppression associated with insufficient epinephrine reserve in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Riepe FG, Krone N, Krüger SN, Sweep FC, Lenders JW, Dötsch J, Mönig H, Sippell WG, Partsch CJ. Riepe FG, et al. Among authors: krone n. Exp Clin Endocrinol Diabetes. 2006 Mar;114(3):105-10. doi: 10.1055/s-2005-865836. Exp Clin Endocrinol Diabetes. 2006. PMID: 16636975

9

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

10

Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis.

Grischuk Y, Rubtsov P, Riepe FG, Grötzinger J, Beljelarskaia S, Prassolov V, Kalintchenko N, Semitcheva T, Peterkova V, Tiulpakov A, Sippell WG, Krone N. Grischuk Y, et al. Among authors: krone n. J Clin Endocrinol Metab. 2006 Dec;91(12):4976-80. doi: 10.1210/jc.2006-0777. Epub 2006 Sep 19. J Clin Endocrinol Metab. 2006. PMID: 16984992

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