Riepe FG - Search Results

1

Hashimoto encephalopathy in a 15-year-old-girl: EEG findings and follow-up.

Muhle H, van Baalen A, Riepe FG, Rohr A, Stephani U. Muhle H, et al. Among authors: riepe fg. Pediatr Neurol. 2009 Oct;41(4):301-4. doi: 10.1016/j.pediatrneurol.2009.04.023. Pediatr Neurol. 2009. PMID: 19748053

2

Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation.

Riepe FG, Partsch CJ, Blankenstein O, Mönig H, Pfäffle RW, Sippell WG. Riepe FG, et al. J Clin Endocrinol Metab. 2001 Sep;86(9):4353-7. doi: 10.1210/jcem.86.9.7828. J Clin Endocrinol Metab. 2001. PMID: 11549674

3

Special feature: picture of the month. Infantile scurvy.

Riepe FG, Eichmann D, Oppermann HC, Schmitt HJ, Tunnessen WW Jr. Riepe FG, et al. Arch Pediatr Adolesc Med. 2001 May;155(5):607-8. doi: 10.1001/archpedi.155.5.607. Arch Pediatr Adolesc Med. 2001. PMID: 11343507 No abstract available.

4

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. Eur J Endocrinol. 2005 Apr;152(4):515-9. doi: 10.1530/eje.1.01879. Eur J Endocrinol. 2005. PMID: 15817905

5

Summary of the workshop "Management of CAH: the relevance of steroids in plasma, saliva and urine".

Riepe F. Riepe F. Pediatr Endocrinol Rev. 2011 Sep;9 Suppl 1:541-3. Pediatr Endocrinol Rev. 2011. PMID: 22423514 No abstract available.

6

[Calcinosis cutis in Albright hereditary osteodystrophy: pseudohypoparathyroidism type Ia].

Fölster-Holst R, Riepe FG, Ahrens W, Möller M, Brasch J, Partsch CJ, Hiort O, Sippell WG. Fölster-Holst R, et al. Among authors: riepe fg. Hautarzt. 2006 Oct;57(10):893-7. doi: 10.1007/s00105-005-1040-4. Hautarzt. 2006. PMID: 16270203 German.

7

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

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

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. Among authors: riepe fg. 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

Disproportionate stature but normal height in hypochondroplasia.

Riepe FG, Krone N, Sippell WG. Riepe FG, et al. 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.

10

Frequency and characterization of DNA methylation defects in children born SGA.

Bens S, Haake A, Richter J, Leohold J, Kolarova J, Vater I, Riepe FG, Buiting K, Eggermann T, Gillessen-Kaesbach G, Platzer K, Prawitt D, Caliebe A, Siebert R. Bens S, et al. Among authors: riepe fg. Eur J Hum Genet. 2013 Aug;21(8):838-43. doi: 10.1038/ejhg.2012.262. Epub 2012 Dec 12. Eur J Hum Genet. 2013. PMID: 23232699 Free PMC article.

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