Riepe F - Search Results

1

Predicting the optimal basal insulin infusion pattern in children and adolescents on insulin pumps.

Holterhus PM, Bokelmann J, Riepe F, Heidtmann B, Wagner V, Rami-Merhar B, Kapellen T, Raile K, Quester W, Holl RW; German/Austrian DPV-Initiative and the German Pediatric CSII Working Group. Holterhus PM, et al. Among authors: riepe f. Diabetes Care. 2013 Jun;36(6):1507-11. doi: 10.2337/dc12-1705. Epub 2013 Feb 12. Diabetes Care. 2013. PMID: 23404300 Free PMC article.

2

Exclusion of serum- and glucocorticoid-induced kinase 1 (SGK1) as a candidate gene for genetically heterogeneous renal pseudohypoaldosteronism type I in eight families.

Riepe FG, Holterhus PM. Riepe FG, et al. Am J Nephrol. 2007;27(2):164-9. doi: 10.1159/000100107. Epub 2007 Feb 23. Am J Nephrol. 2007. PMID: 17317952

3

Transcriptional response of peripheral blood mononuclear cells to recombinant human growth hormone in a routine four-days IGF-I generation test.

Welzel M, Appari M, Bramswig N, Riepe FG, Holterhus PM. Welzel M, et al. Growth Horm IGF Res. 2011 Dec;21(6):336-42. doi: 10.1016/j.ghir.2011.09.001. Epub 2011 Oct 4. Growth Horm IGF Res. 2011. PMID: 21975122

4

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. Horm Res Paediatr. 2013;79(1):22-31. doi: 10.1159/000346406. Epub 2013 Jan 17. Horm Res Paediatr. 2013. PMID: 23328487

5

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

6

In vivo investigations of the effect of short- and long-term recombinant growth hormone treatment on DNA-methylation in humans.

Kolarova J, Ammerpohl O, Gutwein J, Welzel M, Baus I, Riepe FG, Eggermann T, Caliebe A, Holterhus PM, Siebert R, Bens S. Kolarova J, et al. Among authors: riepe fg. PLoS One. 2015 Mar 18;10(3):e0120463. doi: 10.1371/journal.pone.0120463. eCollection 2015. PLoS One. 2015. PMID: 25785847 Free PMC article.

7

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

8

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

9

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. Among authors: riepe f. 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

10

Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.

Menabò S, Polat S, Baldazzi L, Kulle AE, Holterhus PM, Grötzinger J, Fanelli F, Balsamo A, Riepe FG. Menabò S, et al. Among authors: riepe fg. Eur J Hum Genet. 2014 May;22(5):610-6. doi: 10.1038/ejhg.2013.197. Epub 2013 Sep 11. Eur J Hum Genet. 2014. PMID: 24022297 Free PMC article.

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