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Page 1
Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families.
Rouen A, Rogers E, Kerlan V, Delemer B, Catteau-Jonard S, Reznik Y, Gompel A, Cedrin I, Guedj AM, Grouthier V, Brue T, Pienkowski C, Bachelot A, Chantot-Bastaraud S, Rousseau A, Simon T, Kott E, Siffroi JP, Touraine P, Christin-Maitre S. Rouen A, et al. Among authors: kerlan v. Fertil Steril. 2022 Apr;117(4):843-853. doi: 10.1016/j.fertnstert.2021.12.023. Epub 2022 Jan 31. Fertil Steril. 2022. PMID: 35115167 Free article.
Anti-androgen treatments.
Bachelot A, Chabbert-Buffet N, Salenave S, Kerlan V, Galand-Portier MB. Bachelot A, et al. Among authors: kerlan v. Ann Endocrinol (Paris). 2010 Feb;71(1):19-24. doi: 10.1016/j.ando.2009.12.001. Epub 2010 Jan 22. Ann Endocrinol (Paris). 2010. PMID: 20096826 Review.
[Editorial].
Kerlan V, Christin-Maitre S. Kerlan V, et al. Ann Endocrinol (Paris). 2011 Oct;72 Suppl 1:S1. doi: 10.1016/S0003-4266(11)70002-6. Ann Endocrinol (Paris). 2011. PMID: 22008271 French. No abstract available.
Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds.
Tichomirowa MA, Lee M, Barlier A, Daly AF, Marinoni I, Jaffrain-Rea ML, Naves LA, Rodien P, Rohmer V, Faucz FR, Caron P, Estour B, Lecomte P, Borson-Chazot F, Penfornis A, Yaneva M, Guitelman M, Castermans E, Verhaege C, Wémeau JL, Tabarin A, Fajardo Montañana C, Delemer B, Kerlan V, Sadoul JL, Cortet Rudelli C, Archambeaud F, Zacharieva S, Theodoropoulou M, Brue T, Enjalbert A, Bours V, Pellegata NS, Beckers A. Tichomirowa MA, et al. Among authors: kerlan v. Endocr Relat Cancer. 2012 May 3;19(3):233-41. doi: 10.1530/ERC-11-0362. Print 2012 Jun. Endocr Relat Cancer. 2012. PMID: 22291433 Free article.
Hormonal contraception in women at risk of vascular and metabolic disorders: guidelines of the French Society of Endocrinology.
Gourdy P, Bachelot A, Catteau-Jonard S, Chabbert-Buffet N, Christin-Maître S, Conard J, Fredenrich A, Gompel A, Lamiche-Lorenzini F, Moreau C, Plu-Bureau G, Vambergue A, Vergès B, Kerlan V. Gourdy P, et al. Among authors: kerlan v. Ann Endocrinol (Paris). 2012 Nov;73(5):469-87. doi: 10.1016/j.ando.2012.09.001. Epub 2012 Oct 15. Ann Endocrinol (Paris). 2012. PMID: 23078975
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis.
Cuny T, Pertuit M, Sahnoun-Fathallah M, Daly A, Occhi G, Odou MF, Tabarin A, Nunes ML, Delemer B, Rohmer V, Desailloud R, Kerlan V, Chabre O, Sadoul JL, Cogne M, Caron P, Cortet-Rudelli C, Lienhardt A, Raingeard I, Guedj AM, Brue T, Beckers A, Weryha G, Enjalbert A, Barlier A. Cuny T, et al. Among authors: kerlan v. Eur J Endocrinol. 2013 Mar 15;168(4):533-41. doi: 10.1530/EJE-12-0763. Print 2013 Apr. Eur J Endocrinol. 2013. PMID: 23321498 Free article.
Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey.
Bouvattier C, Esterle L, Renoult-Pierre P, de la Perrière AB, Illouz F, Kerlan V, Pascal-Vigneron V, Drui D, Christin-Maitre S, Galland F, Brue T, Reznik Y, Schillo F, Pinsard D, Piguel X, Chabrier G, Decoudier B, Emy P, Tauveron I, Raffin-Sanson ML, Bertherat J, Kuhn JM, Caron P, Cartigny M, Chabre O, Dewailly D, Morel Y, Touraine P, Tardy-Guidollet V, Young J. Bouvattier C, et al. Among authors: kerlan v. J Clin Endocrinol Metab. 2015 Jun;100(6):2303-13. doi: 10.1210/jc.2014-4124. Epub 2015 Mar 30. J Clin Endocrinol Metab. 2015. PMID: 25822101
[Pregnancy-associated hormones and fetal-maternal relations].
Gailly-Fabre E, Kerlan V, Christin-Maitre S. Gailly-Fabre E, et al. Among authors: kerlan v. Ann Endocrinol (Paris). 2015 Oct;76(6 Suppl 1):S39-50. doi: 10.1016/S0003-4266(16)30006-3. Ann Endocrinol (Paris). 2015. PMID: 26776288 Review. French.
Spontaneous fertility and pregnancy outcomes amongst 480 women with Turner syndrome.
Bernard V, Donadille B, Zenaty D, Courtillot C, Salenave S, Brac de la Perrière A, Albarel F, Fèvre A, Kerlan V, Brue T, Delemer B, Borson-Chazot F, Carel JC, Chanson P, Léger J, Touraine P, Christin-Maitre S; CMERC Center for Rare Disease. Bernard V, et al. Among authors: kerlan v. Hum Reprod. 2016 Apr;31(4):782-8. doi: 10.1093/humrep/dew012. Epub 2016 Feb 13. Hum Reprod. 2016. PMID: 26874361
135 results