Brauner R - Search Results

1

Mutations in NR5A1 associated with ovarian insufficiency.

Lourenço D, Brauner R, Lin L, De Perdigo A, Weryha G, Muresan M, Boudjenah R, Guerra-Junior G, Maciel-Guerra AT, Achermann JC, McElreavey K, Bashamboo A. Lourenço D, et al. Among authors: brauner r. N Engl J Med. 2009 Mar 19;360(12):1200-10. doi: 10.1056/NEJMoa0806228. Epub 2009 Feb 25. N Engl J Med. 2009. PMID: 19246354 Free PMC article.

2

[Study of sex determination gene (SRY) in 46,XY gonadal dysgenesis].

Boucekkine C, Vilain E, McElreavey K, Jaubert F, Brauner R, Thibaud E, Battin J, Toublanc JE, Kucheria K, Chaabouni S, et al. Boucekkine C, et al. Among authors: brauner r. Ann Endocrinol (Paris). 1994;54(5):315-21. Ann Endocrinol (Paris). 1994. PMID: 8085778 French.

3

Deletions of distal 9p associated with 46,XY male to female sex reversal: definition of the breakpoints at 9p23.3-p24.1.

Veitia R, Nunes M, Brauner R, Doco-Fenzy M, Joanny-Flinois O, Jaubert F, Lortat-Jacob S, Fellous M, McElreavey K. Veitia R, et al. Among authors: brauner r. Genomics. 1997 Apr 15;41(2):271-4. doi: 10.1006/geno.1997.4648. Genomics. 1997. PMID: 9143505

4

An analysis of the genetic factors involved in testicular descent in a cohort of 14 male patients with anorchia.

Vinci G, Anjot MN, Trivin C, Lottmann H, Brauner R, McElreavey K. Vinci G, et al. Among authors: brauner r. J Clin Endocrinol Metab. 2004 Dec;89(12):6282-5. doi: 10.1210/jc.2004-0891. J Clin Endocrinol Metab. 2004. PMID: 15579790

5

Idiopathic male pseudohermaphroditism: variations in presentation and management.

Meau-Petit V, Marcou V, Trivin C, Lortat-Jacob S, McElreavey K, Brauner R. Meau-Petit V, et al. Among authors: brauner r. J Pediatr Endocrinol Metab. 2005 Jun;18(6):569-75. doi: 10.1515/jpem.2005.18.6.569. J Pediatr Endocrinol Metab. 2005. PMID: 16042324

6

Association of deletion 9p, 46,XY gonadal dysgenesis and autistic spectrum disorder.

Vinci G, Chantot-Bastaraud S, El Houate B, Lortat-Jacob S, Brauner R, McElreavey K. Vinci G, et al. Among authors: brauner r. Mol Hum Reprod. 2007 Sep;13(9):685-9. doi: 10.1093/molehr/gam045. Epub 2007 Jul 20. Mol Hum Reprod. 2007. PMID: 17644778

7

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility.

Vinci G, Brauner R, Tar A, Rouba H, Sheth J, Sheth F, Ravel C, McElreavey K, Bashamboo A. Vinci G, et al. Among authors: brauner r. Fertil Steril. 2009 Oct;92(4):1347-1350. doi: 10.1016/j.fertnstert.2009.04.009. Epub 2009 May 21. Fertil Steril. 2009. PMID: 19463995 Free article.

8

[NR5A1 and ovarian failure].

Bashamboo A, Ravel C, Brauner R, McElreavey K. Bashamboo A, et al. Among authors: brauner r. Med Sci (Paris). 2009 Oct;25(10):809-13. doi: 10.1051/medsci/20092510809. Med Sci (Paris). 2009. PMID: 19849982 Free article. Review. French.

9

Clinical, biological and genetic analysis of prepubertal isolated ovarian cyst in 11 girls.

Brauner R, Bashamboo A, Rouget S, Goulet M, Philibert P, Sarda-Thibault H, Trivin C, Misrahi M, Sultan C, McElreavey K. Brauner R, et al. PLoS One. 2010 Jun 25;5(6):e11282. doi: 10.1371/journal.pone.0011282. PLoS One. 2010. PMID: 20593028 Free PMC article.

10

Loss-of-function mutation in GATA4 causes anomalies of human testicular development.

Lourenço D, Brauner R, Rybczynska M, Nihoul-Fékété C, McElreavey K, Bashamboo A. Lourenço D, et al. Among authors: brauner r. Proc Natl Acad Sci U S A. 2011 Jan 25;108(4):1597-602. doi: 10.1073/pnas.1010257108. Epub 2011 Jan 10. Proc Natl Acad Sci U S A. 2011. PMID: 21220346 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

320 results

Search Page

Filters