Reisch N - Search Results

1

Association of somatoform disorder symptoms with genetic variants potentially involved in the modulation of nociception.

Gil FP, Giegling I, Reisch N, Hartmann AM, Konte B, Schwarz MJ, Rujescu D. Gil FP, et al. Among authors: reisch n. Psychiatr Genet. 2011 Feb;21(1):50. doi: 10.1097/YPG.0b013e3283413602. Psychiatr Genet. 2011. PMID: 21037510 No abstract available.

2

No evidence of association between adrenocorticotropic hormone receptor promoter polymorphism and somatoform disorders.

Pedrosa Gil F, Rottenkolber M, Reisch N. Pedrosa Gil F, et al. Among authors: reisch n. Psychiatr Genet. 2008 Feb;18(1):45. doi: 10.1097/YPG.0b013e3282f089ba. Psychiatr Genet. 2008. PMID: 18197087 No abstract available.

3

High prevalence of reduced fecundity in men with congenital adrenal hyperplasia.

Reisch N, Flade L, Scherr M, Rottenkolber M, Pedrosa Gil F, Bidlingmaier M, Wolff H, Schwarz HP, Quinkler M, Beuschlein F, Reincke M. Reisch N, et al. J Clin Endocrinol Metab. 2009 May;94(5):1665-70. doi: 10.1210/jc.2008-1414. Epub 2009 Mar 3. J Clin Endocrinol Metab. 2009. PMID: 19258407

4

Testicular adrenal rest tumors develop independently of long-term disease control: a longitudinal analysis of 50 adult men with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency.

Reisch N, Rottenkolber M, Greifenstein A, Krone N, Schmidt H, Reincke M, Schwarz HP, Beuschlein F. Reisch N, et al. J Clin Endocrinol Metab. 2013 Nov;98(11):E1820-6. doi: 10.1210/jc.2012-3181. Epub 2013 Aug 22. J Clin Endocrinol Metab. 2013. PMID: 23969190

5

Genetic influence of an ACTH receptor promoter polymorphism on adrenal androgen secretion.

Reisch N, Slawik M, Zwermann O, Beuschlein F, Reincke M. Reisch N, et al. Eur J Endocrinol. 2005 Nov;153(5):711-5. doi: 10.1530/eje.1.02015. Eur J Endocrinol. 2005. PMID: 16260430

6

Characterization of an adrenocorticotropin (ACTH) receptor promoter polymorphism leading to decreased adrenal responsiveness to ACTH.

Slawik M, Reisch N, Zwermann O, Maser-Gluth C, Stahl M, Klink A, Reincke M, Beuschlein F. Slawik M, et al. Among authors: reisch n. J Clin Endocrinol Metab. 2004 Jul;89(7):3131-7. doi: 10.1210/jc.2003-032010. J Clin Endocrinol Metab. 2004. PMID: 15240582

7

The rs1990760 polymorphism within the IFIH1 locus is not associated with Graves' disease, Hashimoto's thyroiditis and Addison's disease.

Penna-Martinez M, Ramos-Lopez E, Robbers I, Kahles H, Hahner S, Willenberg H, Reisch N, Seidl C, Segni M, Badenhoop K. Penna-Martinez M, et al. Among authors: reisch n. BMC Med Genet. 2009 Dec 4;10:126. doi: 10.1186/1471-2350-10-126. BMC Med Genet. 2009. PMID: 19961590 Free PMC article.

8

Total adrenal volume but not testicular adrenal rest tumor volume is associated with hormonal control in patients with 21-hydroxylase deficiency.

Reisch N, Scherr M, Flade L, Bidlingmaier M, Schwarz HP, Müller-Lisse U, Reincke M, Quinkler M, Beuschlein F. Reisch N, et al. J Clin Endocrinol Metab. 2010 May;95(5):2065-72. doi: 10.1210/jc.2009-1929. Epub 2010 Feb 26. J Clin Endocrinol Metab. 2010. PMID: 20190160

9

Quality of life is less impaired in adults with congenital adrenal hyperplasia because of 21-hydroxylase deficiency than in patients with primary adrenal insufficiency.

Reisch N, Hahner S, Bleicken B, Flade L, Pedrosa Gil F, Loeffler M, Ventz M, Hinz A, Beuschlein F, Allolio B, Reincke M, Quinkler M. Reisch N, et al. Clin Endocrinol (Oxf). 2011 Feb;74(2):166-73. doi: 10.1111/j.1365-2265.2010.03920.x. Clin Endocrinol (Oxf). 2011. PMID: 21050254

10

Frequency and causes of adrenal crises over lifetime in patients with 21-hydroxylase deficiency.

Reisch N, Willige M, Kohn D, Schwarz HP, Allolio B, Reincke M, Quinkler M, Hahner S, Beuschlein F. Reisch N, et al. Eur J Endocrinol. 2012 Jul;167(1):35-42. doi: 10.1530/EJE-12-0161. Epub 2012 Apr 18. Eur J Endocrinol. 2012. PMID: 22513882

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