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Clinical management of difficult to treat macroprolactinomas.
Sahakian N, Castinetti F, Dufour H, Graillon T, Romanet P, Barlier A, Brue T, Cuny T. Sahakian N, et al. Among authors: barlier a. Expert Rev Endocrinol Metab. 2019 May;14(3):179-192. doi: 10.1080/17446651.2019.1596024. Epub 2019 Mar 27. Expert Rev Endocrinol Metab. 2019. PMID: 30913932 Free article. Review.
[Pituitary development and pathology of transcription factors].
Barlier A, Vallette-Kasic S, Manavela M, Perez M, Diaz A, Pellegrini-Bouiller I, Enjalbert A, Brue T. Barlier A, et al. Ann Endocrinol (Paris). 2000 Sep;61(3):201-7. Ann Endocrinol (Paris). 2000. PMID: 10970945 Review. French.
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.
Vallette-Kasic S, Barlier A, Teinturier C, Diaz A, Manavela M, Berthezène F, Bouchard P, Chaussain JL, Brauner R, Pellegrini-Bouiller I, Jaquet P, Enjalbert A, Brue T. Vallette-Kasic S, et al. Among authors: barlier a. J Clin Endocrinol Metab. 2001 Sep;86(9):4529-35. doi: 10.1210/jcem.86.9.7811. J Clin Endocrinol Metab. 2001. PMID: 11549703
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.
Vallette-Kasic S, Brue T, Pulichino AM, Gueydan M, Barlier A, David M, Nicolino M, Malpuech G, Déchelotte P, Deal C, Van Vliet G, De Vroede M, Riepe FG, Partsch CJ, Sippell WG, Berberoglu M, Atasay B, de Zegher F, Beckers D, Kyllo J, Donohoue P, Fassnacht M, Hahner S, Allolio B, Noordam C, Dunkel L, Hero M, Pigeon B, Weill J, Yigit S, Brauner R, Heinrich JJ, Cummings E, Riddell C, Enjalbert A, Drouin J. Vallette-Kasic S, et al. Among authors: barlier a. J Clin Endocrinol Metab. 2005 Mar;90(3):1323-31. doi: 10.1210/jc.2004-1300. Epub 2004 Dec 21. J Clin Endocrinol Metab. 2005. PMID: 15613420
191 results