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Page 1
Complete androgen insensitivity syndrome: diagnosis and management.
Cheikhelard A, Thibaud E, Morel Y, Jaubert F, Lortat-Jacob S, Polak M, Nihoul-Fekete C. Cheikhelard A, et al. Expert Rev Endocrinol Metab. 2009 Nov;4(6):565-573. doi: 10.1586/eem.09.31. Expert Rev Endocrinol Metab. 2009. PMID: 30780790
[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.
Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.
de Lonlay P, Simon-Carre A, Ribeiro MJ, Boddaert N, Giurgea I, Laborde K, Bellanné-Chantelot C, Verkarre V, Polak M, Rahier J, Syrota A, Seidenwurm D, Nihoul-Fékété C, Robert JJ, Brunelle F, Jaubert F. de Lonlay P, et al. J Clin Endocrinol Metab. 2006 Mar;91(3):933-40. doi: 10.1210/jc.2005-1713. Epub 2006 Jan 10. J Clin Endocrinol Metab. 2006. PMID: 16403819
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
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. 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.
191 results