Brauner R - Search Results

1

Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.

Bastian C, Muller JB, Lortat-Jacob S, Nihoul-Fékété C, Bignon-Topalovic J, McElreavey K, Bashamboo A, Brauner R. Bastian C, et al. Among authors: brauner r. Fertil Steril. 2015 May;103(5):1297-304. doi: 10.1016/j.fertnstert.2015.01.043. Epub 2015 Mar 23. Fertil Steril. 2015. PMID: 25813279 Free article.

2

True hermaphroditism: genetic variants and clinical management.

Hadjiathanasiou CG, Brauner R, Lortat-Jacob S, Nivot S, Jaubert F, Fellous M, Nihoul-Fékété C, Rappaport R. Hadjiathanasiou CG, et al. Among authors: brauner r. J Pediatr. 1994 Nov;125(5 Pt 1):738-44. doi: 10.1016/s0022-3476(94)70067-2. J Pediatr. 1994. PMID: 7965425 Clinical Trial.

3

[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.

4

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

5

SRY protein is expressed in ovotestis and streak gonads from human sex-reversal.

Salas-Cortés L, Jaubert F, Nihoul-Feketé C, Brauner R, Rosemblatt M, Fellous M. Salas-Cortés L, et al. Among authors: brauner r. Cytogenet Cell Genet. 2000;91(1-4):212-6. doi: 10.1159/000056847. Cytogenet Cell Genet. 2000. PMID: 11173859

6

Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for management.

Pinto G, Tardy V, Trivin C, Thalassinos C, Lortat-Jacob S, Nihoul-Fékété C, Morel Y, Brauner R. Pinto G, et al. Among authors: brauner r. J Clin Endocrinol Metab. 2003 Jun;88(6):2624-33. doi: 10.1210/jc.2002-021433. J Clin Endocrinol Metab. 2003. PMID: 12788866

7

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

8

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

9

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

10

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.

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