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Page 1
French consensus on the management of acromegaly.
Chanson P, Bertherat J, Beckers A, Bihan H, Brue T, Caron P, Chabre O, Cogne M, Cortet-Rudelli C, Delemer B, Dufour H, Gaillard R, Gueydan M, Morange I, Souberbielle JC, Tabarin A; Club Français De L'hypophyse (French Pituitary Club); Société Française Dendocrinologie (French Endocrinology Society). Chanson P, et al. Among authors: gueydan m. Ann Endocrinol (Paris). 2009 Apr;70(2):92-106. doi: 10.1016/j.ando.2008.12.011. Epub 2009 Apr 5. Ann Endocrinol (Paris). 2009. PMID: 19345931 Review. No abstract available.
[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry].
Jaquet P, Cortet-Rudelli Ch, Sassolas G, Morange-Ramos I, Chanson P, Brue T, Andrieu JM, Beckers A, Bertherat J, Borson-Chazot F, Brassier G, Caron P, Cogne M, Cottier JP, Delemer B, Dufour H, Enjalbert A, Figarella-Branger D, Gaillard R, Gueydan M, Jan M, Kuhn JM, Raingeard I, Regis J, Roger P, Rohmer V, Sadoul JL, Saveanu A, Tabarin A, Travers N, Trouillas J; French Acromegly Registry. Jaquet P, et al. Among authors: gueydan m. Ann Endocrinol (Paris). 2003 Dec;64(6):434-41. Ann Endocrinol (Paris). 2003. PMID: 15067248 Review. French.
Aggressive multimodal therapy of sporadic malignant insulinoma can improve survival: a retrospective 35-year study of 12 patients.
Bégu-Le Corroller A, Valéro R, Moutardier V, Henry JF, Le Treut YP, Gueydan M, De Micco C, Sierra M, Conte-Devolx B, Oliver C, Raccah D, Favre R, Digue L, Heim M, Seitz JF, Delpero JR, Vialettes B. Bégu-Le Corroller A, et al. Among authors: gueydan m. Diabetes Metab. 2008 Sep;34(4 Pt 1):343-8. doi: 10.1016/j.diabet.2008.01.013. Epub 2008 Jun 16. Diabetes Metab. 2008. PMID: 18556231
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: gueydan m. 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
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutations.
Vallette-Kasic S, Pulichino AM, Gueydan M, Barlier A, David M, Malpuech G, Deal C, Van Vliet G, de Vroede M, Riepe F, Partsch CJ, Sippell W, Berberoglu M, Atasay B, de Zegher F, Kyllo J, Donohoue P, Dechelotte P, Fassnacht M, Noordam K, Dunkel L, Pigeon B, Weill J, Yigit S, Brauner R, Leger J, Heinrich JJ, Enjalbert A, Brue T, Drouin J. Vallette-Kasic S, et al. Among authors: gueydan m. Endocr Res. 2004 Nov;30(4):943-4. doi: 10.1081/erc-200044166. Endocr Res. 2004. PMID: 15666849 No abstract available.