Bouvattier C - Search Results

1

Functional Characterization of Glucocorticoid Receptor Variants Is Required to Avoid Misinterpretation of NGS Data.

Foussier L, Vitellius G, Bouligand J, Amazit L, Bouvattier C, Young J, Trabado S, Lombès M. Foussier L, et al. Among authors: bouvattier c. J Endocr Soc. 2019 Mar 6;3(5):865-881. doi: 10.1210/js.2019-00028. eCollection 2019 May 1. J Endocr Soc. 2019. PMID: 31008420 Free PMC article.

2

Neonatal gonadotropin therapy in male congenital hypogonadotropic hypogonadism.

Bouvattier C, Maione L, Bouligand J, Dodé C, Guiochon-Mantel A, Young J. Bouvattier C, et al. Nat Rev Endocrinol. 2011 Oct 18;8(3):172-82. doi: 10.1038/nrendo.2011.164. Nat Rev Endocrinol. 2011. PMID: 22009162 Review.

3

Insulin-like peptide 3 (INSL3) in men with congenital hypogonadotropic hypogonadism/Kallmann syndrome and effects of different modalities of hormonal treatment: a single-center study of 281 patients.

Trabado S, Maione L, Bry-Gauillard H, Affres H, Salenave S, Sarfati J, Bouvattier C, Delemer B, Chanson P, Le Bouc Y, Brailly-Tabard S, Young J. Trabado S, et al. Among authors: bouvattier c. J Clin Endocrinol Metab. 2014 Feb;99(2):E268-75. doi: 10.1210/jc.2013-2288. Epub 2013 Nov 15. J Clin Endocrinol Metab. 2014. PMID: 24243640

4

Congenital hypogonadotropic hypogonadism and Kallmann syndrome as models for studying hormonal regulation of human testicular endocrine functions.

Trabado S, Lamothe S, Maione L, Bouvattier C, Sarfati J, Brailly-Tabard S, Young J. Trabado S, et al. Among authors: bouvattier c. Ann Endocrinol (Paris). 2014 May;75(2):79-87. doi: 10.1016/j.ando.2014.04.011. Epub 2014 May 9. Ann Endocrinol (Paris). 2014. PMID: 24815726 Review.

5

Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.

Sarfati J, Bouvattier C, Bry-Gauillard H, Cartes A, Bouligand J, Young J. Sarfati J, et al. Among authors: bouvattier c. Orphanet J Rare Dis. 2015 Jun 9;10:71. doi: 10.1186/s13023-015-0287-9. Orphanet J Rare Dis. 2015. PMID: 26051373 Free PMC article.

6

Prevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study.

Francou B, Paul C, Amazit L, Cartes A, Bouvattier C, Albarel F, Maiter D, Chanson P, Trabado S, Brailly-Tabard S, Brue T, Guiochon-Mantel A, Young J, Bouligand J. Francou B, et al. Among authors: bouvattier c. Hum Reprod. 2016 Jun;31(6):1363-74. doi: 10.1093/humrep/dew073. Epub 2016 Apr 19. Hum Reprod. 2016. PMID: 27094476

7

Multiplexed steroid profiling of gluco- and mineralocorticoids pathways using a liquid chromatography tandem mass spectrometry method.

Travers S, Martinerie L, Bouvattier C, Boileau P, Lombès M, Pussard E. Travers S, et al. Among authors: bouvattier c. J Steroid Biochem Mol Biol. 2017 Jan;165(Pt B):202-211. doi: 10.1016/j.jsbmb.2016.06.005. Epub 2016 Jun 23. J Steroid Biochem Mol Biol. 2017. PMID: 27339652

8

[Differences of Sex Development (DSD): Controversies and Challenges].

Bessiène L, Lombès M, Bouvattier C. Bessiène L, et al. Among authors: bouvattier c. Ann Endocrinol (Paris). 2018 Sep;79 Suppl 1:S22-S30. doi: 10.1016/S0003-4266(18)31235-6. Ann Endocrinol (Paris). 2018. PMID: 30213302 Review. French.

9

Foetal exposure to mitotane/Op'DDD: Post-natal study of four children.

Magkou D, Do Cao C, Bouvattier C, Douillard C, de Marcellus C, Cazabat L, Gérard M, Raffin-Sanson ML, Young J. Magkou D, et al. Among authors: bouvattier c. Clin Endocrinol (Oxf). 2018 Dec;89(6):805-812. doi: 10.1111/cen.13854. Epub 2018 Oct 16. Clin Endocrinol (Oxf). 2018. PMID: 30222204

10

Pubertal growth spurt in patients with bilateral anorchia after testosterone replacement therapy.

Fouatih K, Belin F, Lambert AS, Bouligand J, Bouvattier C. Fouatih K, et al. Among authors: bouvattier c. Arch Pediatr. 2019 Sep;26(6):320-323. doi: 10.1016/j.arcped.2019.06.008. Epub 2019 Jul 25. Arch Pediatr. 2019. PMID: 31353150

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