De Baere E - Search Results

1

A novel mutation c.118delA in exon 1 of the androgen receptor gene resulting in complete androgen insensitivity syndrome within a large family.

Decaestecker K, Philibert P, De Baere E, Hoebeke P, Kaufman JM, Sultan C, T'Sjoen G. Decaestecker K, et al. Among authors: de baere e. Fertil Steril. 2008 May;89(5):1260.e3-1260.e7. doi: 10.1016/j.fertnstert.2007.04.057. Epub 2007 Aug 21. Fertil Steril. 2008. PMID: 17714709 Free article.

2

Gender identity disorder in twins: a review of the case report literature.

Heylens G, De Cuypere G, Zucker KJ, Schelfaut C, Elaut E, Vanden Bossche H, De Baere E, T'Sjoen G. Heylens G, et al. Among authors: de cuypere g, de baere e. J Sex Med. 2012 Mar;9(3):751-7. doi: 10.1111/j.1743-6109.2011.02567.x. Epub 2011 Dec 6. J Sex Med. 2012. PMID: 22146048 Review.

3

Extensive clinical, hormonal and genetic screening in a large consecutive series of 46,XY neonates and infants with atypical sexual development.

Baetens D, Mladenov W, Delle Chiaie B, Menten B, Desloovere A, Iotova V, Callewaert B, Van Laecke E, Hoebeke P, De Baere E, Cools M. Baetens D, et al. Among authors: de baere e. Orphanet J Rare Dis. 2014 Dec 14;9:209. doi: 10.1186/s13023-014-0209-2. Orphanet J Rare Dis. 2014. PMID: 25497574 Free PMC article.

4

Mother and daughter became father and son: a case report.

Sajevets T, Verroken C, Heylens G, De Baere E, T'Sjoen G. Sajevets T, et al. Among authors: de baere e. Asian J Androl. 2015 Sep-Oct;17(5):855-6. doi: 10.4103/1008-682X.145430. Asian J Androl. 2015. PMID: 25652622 Free PMC article. No abstract available.

5

Endocrine outcome and seminal parameters in young adult men born with hypospadias: A cross-sectional cohort study.

Tack LJW, Spinoit AF, Hoebeke P, Riedl S, Springer A, Tonnhofer U, Hiess M, Weninger J, Mahmoud A, Tilleman K, Van Laecke E, Juul A, Albrethsen J, De Baere E, Van De Velde J, Verdin H, Cools M. Tack LJW, et al. Among authors: de baere e. EBioMedicine. 2022 Jul;81:104119. doi: 10.1016/j.ebiom.2022.104119. Epub 2022 Jun 24. EBioMedicine. 2022. PMID: 35759917 Free PMC article.

6

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation.

De Baere E, Beysen D, Oley C, Lorenz B, Cocquet J, De Sutter P, Devriendt K, Dixon M, Fellous M, Fryns JP, Garza A, Jonsrud C, Koivisto PA, Krause A, Leroy BP, Meire F, Plomp A, Van Maldergem L, De Paepe A, Veitia R, Messiaen L. De Baere E, et al. Among authors: de paepe a, de sutter p. Am J Hum Genet. 2003 Feb;72(2):478-87. doi: 10.1086/346118. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529855 Free PMC article.

7

The human FOXL2 mutation database.

Beysen D, Vandesompele J, Messiaen L, De Paepe A, De Baere E. Beysen D, et al. Among authors: de paepe a, de baere e. Hum Mutat. 2004 Sep;24(3):189-93. doi: 10.1002/humu.20079. Hum Mutat. 2004. PMID: 15300845

8

Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.

De Baere E, Copelli S, Caburet S, Laissue P, Beysen D, Christin-Maitre S, Bouchard P, Veitia R, Fellous M. De Baere E, et al. Pediatr Endocrinol Rev. 2005 Jun;2(4):653-60. Pediatr Endocrinol Rev. 2005. PMID: 16208278 Review.

9

Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa.

Coppieters F, Leroy BP, Beysen D, Hellemans J, De Bosscher K, Haegeman G, Robberecht K, Wuyts W, Coucke PJ, De Baere E. Coppieters F, et al. Among authors: de bosscher k, de baere e. Am J Hum Genet. 2007 Jul;81(1):147-57. doi: 10.1086/518426. Epub 2007 May 24. Am J Hum Genet. 2007. PMID: 17564971 Free PMC article.

10

Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.

Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, Decock C, Delbeke P, Ensenauer R, Ebinger F, Gillessen-Kaesbach G, Hendriks Y, Kimonis V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: de jaegere s, de paepe a, de ravel t, de baere e. Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819. Hum Mutat. 2008. PMID: 18642388

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