Jaubert F - Search Results

1

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: jaubert f. 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.

2

[Hermaphroditism pathology].

Jaubert F, Nihoul-Fékété C, Lortat-Jacob S, Josso N, Fellous M. Jaubert F, et al. Ann Pathol. 2004 Dec;24(6):499-509. doi: 10.1016/s0242-6498(04)94014-x. Ann Pathol. 2004. PMID: 15785398 Review. French.

3

Hermaphroditism pathology.

Jaubert F, Nihoul-Fékété C, Lortat-Jacob S, Josso N, Fellous M. Jaubert F, et al. Rom J Morphol Embryol. 1999-2004;45:41-51. Rom J Morphol Embryol. 1999. PMID: 15847378 Review.

4

Aetiological diagnosis of male sex ambiguity: a collaborative study.

Morel Y, Rey R, Teinturier C, Nicolino M, Michel-Calemard L, Mowszowicz I, Jaubert F, Fellous M, Chaussain JL, Chatelain P, David M, Nihoul-Fékété C, Forest MG, Josso N. Morel Y, et al. Among authors: jaubert f. Eur J Pediatr. 2002 Jan;161(1):49-59. doi: 10.1007/s00431-001-0854-z. Eur J Pediatr. 2002. PMID: 11808880 Review.

5

Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes).

Auber F, Lortat-Jacob S, Sarnacki S, Jaubert F, Salomon R, Thibaud E, Jeanpierre C, Nihoul-Fékété C. Auber F, et al. Among authors: jaubert f. J Pediatr Surg. 2003 Jan;38(1):124-9; discussion 124-9. doi: 10.1053/jpsu.2003.50025. J Pediatr Surg. 2003. PMID: 12592634

6

The long-term followup of 33 cases of true hermaphroditism: a 40-year experience with conservative gonadal surgery.

Verkauskas G, Jaubert F, Lortat-Jacob S, Malan V, Thibaud E, Nihoul-Fékété C. Verkauskas G, et al. Among authors: jaubert f. J Urol. 2007 Feb;177(2):726-31; discussion 731. doi: 10.1016/j.juro.2006.10.003. J Urol. 2007. PMID: 17222668

7

Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome.

Abbas N, McElreavey K, Leconiat M, Vilain E, Jaubert F, Berger R, Nihoul-Fekete C, Rappaport R, Fellous M. Abbas N, et al. Among authors: jaubert f. C R Acad Sci III. 1993;316(4):375-83. C R Acad Sci III. 1993. PMID: 8402263

8

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: jaubert f. Genomics. 1997 Apr 15;41(2):271-4. doi: 10.1006/geno.1997.4648. Genomics. 1997. PMID: 9143505

9

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: jaubert f. Cytogenet Cell Genet. 2000;91(1-4):212-6. doi: 10.1159/000056847. Cytogenet Cell Genet. 2000. PMID: 11173859

10

Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.

Cheikhelard A, Morel Y, Thibaud E, Lortat-Jacob S, Jaubert F, Polak M, Nihoul-Fekete C. Cheikhelard A, et al. Among authors: jaubert f. J Urol. 2008 Oct;180(4):1496-501. doi: 10.1016/j.juro.2008.06.045. Epub 2008 Aug 16. J Urol. 2008. PMID: 18710728

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