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Genetic testing in prolactinomas: a cohort study.
Boukerrouni A, Cuny T, Anjou T, Raingeard I, Ferrière A, Grunenwald S, Maïza JC, Marquant E, Sahakian N, Fodil-Cherif S, Salle L, Niccoli P, Randrianaivo H, Sonnet E, Chevalier N, Thuillier P, Vezzosi D, Reynaud R, Dufour H, Brue T, Tabarin A, Delemer B, Kerlan V, Castinetti F, Barlier A, Romanet P. Boukerrouni A, et al. Among authors: reynaud r. Eur J Endocrinol. 2023 Dec 6;189(6):567-574. doi: 10.1093/ejendo/lvad148. Eur J Endocrinol. 2023. PMID: 37956455
Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency.
Turton JP, Reynaud R, Mehta A, Torpiano J, Saveanu A, Woods KS, Tiulpakov A, Zdravkovic V, Hamilton J, Attard-Montalto S, Parascandalo R, Vella C, Clayton PE, Shalet S, Barton J, Brue T, Dattani MT. Turton JP, et al. Among authors: reynaud r. J Clin Endocrinol Metab. 2005 Aug;90(8):4762-70. doi: 10.1210/jc.2005-0570. Epub 2005 May 31. J Clin Endocrinol Metab. 2005. PMID: 15928241
[Genetics of anterior hypopituitary diseases].
Reynaud R, Barlier A, Saveanu A, Quentien MH, Enjalbert A, Brue T. Reynaud R, et al. Ann Endocrinol (Paris). 2005 Jun;66(3):250-7. doi: 10.1016/s0003-4266(05)81758-5. Ann Endocrinol (Paris). 2005. PMID: 15988387 Review. French. No abstract available.
[Clinical and genetic aspects of combined pituitary hormone deficiencies].
Castinetti F, Reynaud R, Saveanu A, Quentien MH, Albarel F, Barlier A, Enjalbert A, Brue T. Castinetti F, et al. Among authors: reynaud r. Ann Endocrinol (Paris). 2008 Feb;69(1):7-17. doi: 10.1016/j.ando.2008.01.001. Epub 2008 Mar 4. Ann Endocrinol (Paris). 2008. PMID: 18291347 Review. French.
207 results