Kliesch S - Search Results

1

A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.

Okutman O, Muller J, Skory V, Garnier JM, Gaucherot A, Baert Y, Lamour V, Serdarogullari M, Gultomruk M, Röpke A, Kliesch S, Herbepin V, Aknin I, Benkhalifa M, Teletin M, Bakircioglu E, Goossens E, Charlet-Berguerand N, Bahceci M, Tüttelmann F, Viville S. Okutman O, et al. Among authors: kliesch s. J Assist Reprod Genet. 2017 May;34(5):683-694. doi: 10.1007/s10815-017-0900-z. Epub 2017 Apr 11. J Assist Reprod Genet. 2017. PMID: 28401488 Free PMC article.

2

[Genetics of male infertility].

Tüttelmann F, Gromoll J, Kliesch S. Tüttelmann F, et al. Among authors: kliesch s. Urologe A. 2008 Dec;47(12):1561-2, 1564-7. doi: 10.1007/s00120-008-1804-4. Urologe A. 2008. PMID: 18953522 Review. German.

3

Aquaporins in the human testis and spermatozoa - identification, involvement in sperm volume regulation and clinical relevance.

Yeung CH, Callies C, Tüttelmann F, Kliesch S, Cooper TG. Yeung CH, et al. Among authors: kliesch s. Int J Androl. 2010 Aug 1;33(4):629-41. doi: 10.1111/j.1365-2605.2009.00998.x. Epub 2009 Oct 12. Int J Androl. 2010. PMID: 19840149

4

Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy.

Tüttelmann F, Werny F, Cooper TG, Kliesch S, Simoni M, Nieschlag E. Tüttelmann F, et al. Among authors: kliesch s. Int J Androl. 2011 Aug;34(4):291-8. doi: 10.1111/j.1365-2605.2010.01087.x. Epub 2010 Jun 28. Int J Androl. 2011. PMID: 20609027

5

Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.

Tüttelmann F, Simoni M, Kliesch S, Ledig S, Dworniczak B, Wieacker P, Röpke A. Tüttelmann F, et al. Among authors: kliesch s. PLoS One. 2011 Apr 29;6(4):e19426. doi: 10.1371/journal.pone.0019426. PLoS One. 2011. PMID: 21559371 Free PMC article.

6

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.

Röpke A, Tewes AC, Gromoll J, Kliesch S, Wieacker P, Tüttelmann F. Röpke A, et al. Among authors: kliesch s. Eur J Hum Genet. 2013 Sep;21(9):1012-5. doi: 10.1038/ejhg.2012.290. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299922 Free PMC article.

7

DNA methylation in spermatozoa as a prospective marker in andrology.

Kläver R, Tüttelmann F, Bleiziffer A, Haaf T, Kliesch S, Gromoll J. Kläver R, et al. Among authors: kliesch s. Andrology. 2013 Sep;1(5):731-40. doi: 10.1111/j.2047-2927.2013.00118.x. Andrology. 2013. PMID: 23970452 Free article.

8

Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case report.

Röpke A, Stratis Y, Dossow-Scheele D, Wieacker P, Kliesch S, Tüttelmann F. Röpke A, et al. Among authors: kliesch s. J Assist Reprod Genet. 2013 Dec;30(12):1553-8. doi: 10.1007/s10815-013-0122-y. Epub 2013 Oct 24. J Assist Reprod Genet. 2013. PMID: 24154799 Free PMC article. No abstract available.

9

Restoration of fertility by gonadotropin replacement in a man with hypogonadotropic azoospermia and testicular adrenal rest tumors due to untreated simple virilizing congenital adrenal hyperplasia.

Rohayem J, Tüttelmann F, Mallidis C, Nieschlag E, Kliesch S, Zitzmann M. Rohayem J, et al. Among authors: kliesch s. Eur J Endocrinol. 2014 Mar 13;170(4):K11-7. doi: 10.1530/EJE-13-0449. Print 2014 Apr. Eur J Endocrinol. 2014. PMID: 24394723

10

DMRT1 mutations are rarely associated with male infertility.

Tewes AC, Ledig S, Tüttelmann F, Kliesch S, Wieacker P. Tewes AC, et al. Among authors: kliesch s. Fertil Steril. 2014 Sep;102(3):816-820.e3. doi: 10.1016/j.fertnstert.2014.05.022. Epub 2014 Jun 14. Fertil Steril. 2014. PMID: 24934491 Free article.

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