Thibaud E - Search Results

1

[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: thibaud e. Ann Endocrinol (Paris). 1994;54(5):315-21. Ann Endocrinol (Paris). 1994. PMID: 8085778 French.

2

XY sex reversal associated with a deletion 5' to the SRY "HMG box" in the testis-determining region.

McElreavy K, Vilain E, Abbas N, Costa JM, Souleyreau N, Kucheria K, Boucekkine C, Thibaud E, Brauner R, Flamant F, et al. McElreavy K, et al. Among authors: thibaud e. Proc Natl Acad Sci U S A. 1992 Nov 15;89(22):11016-20. doi: 10.1073/pnas.89.22.11016. Proc Natl Acad Sci U S A. 1992. PMID: 1438307 Free PMC article.

3

Donor splice-site mutations in WT1 are responsible for Frasier syndrome.

Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fékété CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K. Barbaux S, et al. Among authors: thibaud e. Nat Genet. 1997 Dec;17(4):467-70. doi: 10.1038/ng1297-467. Nat Genet. 1997. PMID: 9398852

4

[Gonadal function after cancer treatments in childhood].

Brauner R, Thibaud E, Rappaport R. Brauner R, et al. Among authors: thibaud e. Ann Pediatr (Paris). 1990 Sep;37(7):437-43. Ann Pediatr (Paris). 1990. PMID: 2256638 Review. French.

5

Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome.

Veitia RA, Nunes M, Quintana-Murci L, Rappaport R, Thibaud E, Jaubert F, Fellous M, McElreavey K, Gonçalves J, Silva M, Rodrigues JC, Caspurro M, Boieiro F, Marques R, Lavinha J. Veitia RA, et al. Among authors: thibaud e. Am J Hum Genet. 1998 Sep;63(3):901-5. doi: 10.1086/302023. Am J Hum Genet. 1998. PMID: 9718353 Free PMC article. No abstract available.

6

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: thibaud e. J Pediatr Surg. 2003 Jan;38(1):124-9; discussion 124-9. doi: 10.1053/jpsu.2003.50025. J Pediatr Surg. 2003. PMID: 12592634

7

[Spontaneously regressive central precocious puberty in girls. Impact on therapeutic indications in precocious puberty].

Brauner R, Thibaud E, Rappaport R. Brauner R, et al. Among authors: thibaud e. Ann Pediatr (Paris). 1987 Jan;34(1):70-4. Ann Pediatr (Paris). 1987. PMID: 3827110 French. No abstract available.

8

[Precocious puberty. Comment on the diagnostic conditions and etiological aspects].

Brauner R, Thibaud E, Pomarede R, Cachin O, Hausser C, Czernichow P, Rappaport R. Brauner R, et al. Among authors: thibaud e. Ann Endocrinol (Paris). 1982 Dec;43(6):497-508. Ann Endocrinol (Paris). 1982. PMID: 7183238 French.

9

Factors affecting gonadal function after bone marrow transplantation during childhood.

Couto-Silva AC, Trivin C, Thibaud E, Esperou H, Michon J, Brauner R. Couto-Silva AC, et al. Among authors: thibaud e. Bone Marrow Transplant. 2001 Jul;28(1):67-75. doi: 10.1038/sj.bmt.1703089. Bone Marrow Transplant. 2001. PMID: 11498747

10

Neonatal bilateral ovarian sex cord stromal tumors.

Capito C, Flechtner I, Thibaud E, Emond S, Kalfa N, Jaubert F, Sarnacki S. Capito C, et al. Among authors: thibaud e. Pediatr Blood Cancer. 2009 Mar;52(3):401-3. doi: 10.1002/pbc.21775. Pediatr Blood Cancer. 2009. PMID: 19058207

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