Richter-Unruh A - Search Results

1

Needle-Free and Needle-Based Growth Hormone Therapy in Children: A Pooled Analysis of Three Long-Term Observational Studies.

Rohrer TR, Ceplis-Kastner S, Jorch N, Müller HL, Pfäffle R, Reinehr T, Richter-Unruh A, Weißenbacher C, Holterhus PM, Ferring Arzneimittel GmbH DSC. Rohrer TR, et al. Horm Res Paediatr. 2018;90(6):393-406. doi: 10.1159/000496614. Epub 2019 Mar 5. Horm Res Paediatr. 2018. PMID: 30836359 Free PMC article. Clinical Trial.

2

Venous sampling can be crucial in identifying the testicular origin of idiopathic male luteinising hormone-independent sexual precocity.

Richter-Unruh A, Jorch N, Wessels HT, Weber EA, Hauffa BP. Richter-Unruh A, et al. Eur J Pediatr. 2002 Dec;161(12):668-71. doi: 10.1007/s00431-002-1094-6. Epub 2002 Nov 6. Eur J Pediatr. 2002. PMID: 12447668

3

Short stature in children with an apparently normal male phenotype can be caused by 45,X/46,XY mosaicism and is susceptible to growth hormone treatment.

Richter-Unruh A, Knauer-Fischer S, Kaspers S, Albrecht B, Gillessen-Kaesbach G, Hauffa BP. Richter-Unruh A, et al. Eur J Pediatr. 2004 Apr;163(4-5):251-6. doi: 10.1007/s00431-004-1406-0. Epub 2004 Feb 18. Eur J Pediatr. 2004. PMID: 14986122

4

Novel insertion frameshift mutation of the LH receptor gene: problematic clinical distinction of Leydig cell hypoplasia from enzyme defects primarily affecting testosterone biosynthesis.

Richter-Unruh A, Korsch E, Hiort O, Holterhus PM, Themmen AP, Wudy SA. Richter-Unruh A, et al. Eur J Endocrinol. 2005 Feb;152(2):255-9. doi: 10.1530/eje.1.01852. Eur J Endocrinol. 2005. PMID: 15745934

5

Clinical characteristics of type 2 diabetes mellitus in overweight European caucasian adolescents.

Reinehr T, Andler W, Kapellen T, Kiess W, Richter-Unruh A, Schönau E, Seewi O, Heinze E, Wabitsch M. Reinehr T, et al. Exp Clin Endocrinol Diabetes. 2005 Mar;113(3):167-70. doi: 10.1055/s-2005-837522. Exp Clin Endocrinol Diabetes. 2005. PMID: 15789276

6

Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome.

Holterhus PM, Deppe U, Werner R, Richter-Unruh A, Bebermeier JH, Wünsch L, Krege S, Schweikert HU, Demeter J, Riepe F, Hiort O, Brooks JD. Holterhus PM, et al. BMC Genomics. 2007 Oct 18;8:376. doi: 10.1186/1471-2164-8-376. BMC Genomics. 2007. PMID: 17945006 Free PMC article.

7

Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palate.

Jochumsen U, Werner R, Miura N, Richter-Unruh A, Hiort O, Holterhus PM. Jochumsen U, et al. Sex Dev. 2008;2(6):302-8. doi: 10.1159/000195679. Epub 2009 Mar 10. Sex Dev. 2008. PMID: 19276632 Free PMC article.

8

Disorders of sex development expose transcriptional autonomy of genetic sex and androgen-programmed hormonal sex in human blood leukocytes.

Holterhus PM, Bebermeier JH, Werner R, Demeter J, Richter-Unruh A, Cario G, Appari M, Siebert R, Riepe F, Brooks JD, Hiort O. Holterhus PM, et al. BMC Genomics. 2009 Jul 1;10:292. doi: 10.1186/1471-2164-10-292. BMC Genomics. 2009. PMID: 19570224 Free PMC article.

9

Novel Insights into 46,XY Disorders of Sex Development due to NR5A1 Gene Mutation.

Werner R, Mönig I, August J, Freiberg C, Lünstedt R, Reiz B, Wünsch L, Holterhus PM, Kulle A, Döhnert U, Wudy SA, Richter-Unruh A, Thorns C, Hiort O. Werner R, et al. Sex Dev. 2015;9(5):260-8. doi: 10.1159/000442309. Epub 2015 Dec 18. Sex Dev. 2015. PMID: 26681172

10

Effects of growth hormone treatment on adult height in severely short children with X-linked hypophosphatemic rickets.

Meyerhoff N, Haffner D, Staude H, Wühl E, Marx M, Beetz R, Querfeld U, Holder M, Billing H, Rabl W, Schröder C, Hiort O, Brämswig JH, Richter-Unruh A, Schnabel D, Živičnjak M; Hypophosphatemic Rickets Study Group of the “Deutsche Gesellschaft für Kinderendokrinologie und -diabetologie” and “Gesellschaft für Pädiatrische Nephrologie”. Meyerhoff N, et al. Pediatr Nephrol. 2018 Mar;33(3):447-456. doi: 10.1007/s00467-017-3820-3. Epub 2017 Oct 20. Pediatr Nephrol. 2018. PMID: 29058153 Clinical Trial.

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