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Impaired puberty, fertility, and final stature in 45,X/46,XY mixed gonadal dysgenetic patients raised as boys.
Martinerie L, Morel Y, Gay CL, Pienkowski C, de Kerdanet M, Cabrol S, Lecointre C, Coutant R, Baron S, Colle M, Brauner R, Thibaud E, Leger J, Nihoul-Fekete C, Bouvattier C. Martinerie L, et al. Among authors: nihoul fekete c. Eur J Endocrinol. 2012 Apr;166(4):687-94. doi: 10.1530/EJE-11-0756. Epub 2012 Jan 11. Eur J Endocrinol. 2012. PMID: 22236473
Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias.
Allali S, Muller JB, Brauner R, Lourenço D, Boudjenah R, Karageorgou V, Trivin C, Lottmann H, Lortat-Jacob S, Nihoul-Fékété C, De Dreuzy O, McElreavey K, Bashamboo A. Allali S, et al. Among authors: nihoul fekete c. PLoS One. 2011;6(10):e24117. doi: 10.1371/journal.pone.0024117. Epub 2011 Oct 20. PLoS One. 2011. PMID: 22028768 Free PMC article.
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: nihoul fekete c. 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.
The surgical management of atypical forms of congenital hyperinsulinism.
Capito C, de Lonlay P, Verkarre V, Jaubert F, Rahier J, Nihoul-Fékété C, Aigrain Y. Capito C, et al. Among authors: nihoul fekete c. Semin Pediatr Surg. 2011 Feb;20(1):54-5. doi: 10.1053/j.sempedsurg.2010.10.003. Semin Pediatr Surg. 2011. PMID: 21186006
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
Bellanné-Chantelot C, Saint-Martin C, Ribeiro MJ, Vaury C, Verkarre V, Arnoux JB, Valayannopoulos V, Gobrecht S, Sempoux C, Rahier J, Fournet JC, Jaubert F, Aigrain Y, Nihoul-Fékété C, de Lonlay P. Bellanné-Chantelot C, et al. Among authors: nihoul fekete c. J Med Genet. 2010 Nov;47(11):752-9. doi: 10.1136/jmg.2009.075416. Epub 2010 Aug 3. J Med Genet. 2010. PMID: 20685672
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