Riepe FG - Search Results

1

LC-MS/MS based determination of basal- and ACTH-stimulated plasma concentrations of 11 steroid hormones: implications for detecting heterozygote CYP21A2 mutation carriers.

Kulle AE, Riepe FG, Hedderich J, Sippell WG, Schmitz J, Niermeyer L, Holterhus PM. Kulle AE, et al. Among authors: riepe fg. Eur J Endocrinol. 2015 Oct;173(4):517-24. doi: 10.1530/EJE-14-1084. Eur J Endocrinol. 2015. PMID: 26315375

2

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

3

Implementation of a liquid chromatography tandem mass spectrometry assay for eight adrenal C-21 steroids and pediatric reference data.

Kulle AE, Welzel M, Holterhus PM, Riepe FG. Kulle AE, et al. Among authors: riepe fg. Horm Res Paediatr. 2013;79(1):22-31. doi: 10.1159/000346406. Epub 2013 Jan 17. Horm Res Paediatr. 2013. PMID: 23328487

4

A novel ultrapressure liquid chromatography tandem mass spectrometry method for the simultaneous determination of androstenedione, testosterone, and dihydrotestosterone in pediatric blood samples: age- and sex-specific reference data.

Kulle AE, Riepe FG, Melchior D, Hiort O, Holterhus PM. Kulle AE, et al. Among authors: riepe fg. J Clin Endocrinol Metab. 2010 May;95(5):2399-409. doi: 10.1210/jc.2009-1670. Epub 2010 Mar 3. J Clin Endocrinol Metab. 2010. PMID: 20200336

5

Principles and clinical applications of liquid chromatography - tandem mass spectrometry for the determination of adrenal and gonadal steroid hormones.

Kulle AE, Welzel M, Holterhus PM, Riepe FG. Kulle AE, et al. Among authors: riepe fg. J Endocrinol Invest. 2011 Oct;34(9):702-8. doi: 10.3275/7843. Epub 2011 Jul 5. J Endocrinol Invest. 2011. PMID: 21738000 Review.

6

Steroid hormone profiles in prepubertal obese children before and after weight loss.

Reinehr T, Kulle A, Wolters B, Lass N, Welzel M, Riepe F, Holterhus PM. Reinehr T, et al. J Clin Endocrinol Metab. 2013 Jun;98(6):E1022-30. doi: 10.1210/jc.2013-1173. Epub 2013 May 23. J Clin Endocrinol Metab. 2013. PMID: 23703723

7

Adrenal and Ovarian Phenotype of a Tissue-Specific Urocortin 2-Overexpressing Mouse Model.

Spyroglou A, Riester A, Mueller-Peltzer K, Lu A, Rohde J, Hantel C, Kuehne C, Kulle A, Riepe F, Deussing JM, Beuschlein F. Spyroglou A, et al. Endocrinology. 2015 Jul;156(7):2646-56. doi: 10.1210/en.2014-1971. Epub 2015 May 5. Endocrinology. 2015. PMID: 25942073

8

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. Among authors: riepe fg. 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

9

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. Endocrinology. 2005 Jun;146(6):2563-74. doi: 10.1210/en.2004-1563. Epub 2005 Feb 24. Endocrinology. 2005. PMID: 15731361

10

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. Among authors: riepe fg. 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

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