Krone N - Search Results

1

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.

2

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

3

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.

4

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

5

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

6

Disproportionate stature but normal height in hypochondroplasia.

Riepe FG, Krone N, Sippell WG. Riepe FG, et al. Among authors: krone n. Eur J Pediatr. 2005 Jun;164(6):397-9. doi: 10.1007/s00431-005-1640-0. Epub 2005 Mar 15. Eur J Pediatr. 2005. PMID: 15909185 No abstract available.

7

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

8

The residue E351 is essential for the activity of human 21-hydroxylase: evidence from a naturally occurring novel point mutation compared with artificial mutants generated by single amino acid substitutions.

Krone N, Riepe FG, Grötzinger J, Partsch CJ, Brämswig J, Sippell WG. Krone N, et al. J Mol Med (Berl). 2005 Jul;83(7):561-8. doi: 10.1007/s00109-005-0655-3. Epub 2005 Apr 14. J Mol Med (Berl). 2005. PMID: 15830218

9

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

10

Three novel point mutations of the CYP21 gene detected in classical forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Krone N, Riepe FG, Partsch CJ, Vorhoff W, Brämswig J, Sippell WG. Krone N, et al. Exp Clin Endocrinol Diabetes. 2006 Mar;114(3):111-7. doi: 10.1055/s-2005-872841. Exp Clin Endocrinol Diabetes. 2006. PMID: 16636976

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