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Page 1
Pathophysiology of renal calcium handling in acromegaly: what lies behind hypercalciuria?
Kamenický P, Blanchard A, Gauci C, Salenave S, Letierce A, Lombès M, Brailly-Tabard S, Azizi M, Prié D, Souberbielle JC, Chanson P. Kamenický P, et al. Among authors: lombes m. J Clin Endocrinol Metab. 2012 Jun;97(6):2124-33. doi: 10.1210/jc.2011-3188. Epub 2012 Apr 10. J Clin Endocrinol Metab. 2012. PMID: 22496496 Clinical Trial.
Lack of androgen receptor expression in Sertoli cells accounts for the absence of anti-Mullerian hormone repression during early human testis development.
Boukari K, Meduri G, Brailly-Tabard S, Guibourdenche J, Ciampi ML, Massin N, Martinerie L, Picard JY, Rey R, Lombès M, Young J. Boukari K, et al. Among authors: lombes m. J Clin Endocrinol Metab. 2009 May;94(5):1818-25. doi: 10.1210/jc.2008-1909. Epub 2009 Mar 10. J Clin Endocrinol Metab. 2009. PMID: 19276236 Free PMC article.
Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation.
Bouligand J, Ghervan C, Tello JA, Brailly-Tabard S, Salenave S, Chanson P, Lombès M, Millar RP, Guiochon-Mantel A, Young J. Bouligand J, et al. Among authors: lombes m. N Engl J Med. 2009 Jun 25;360(26):2742-8. doi: 10.1056/NEJMoa0900136. Epub 2009 Jun 17. N Engl J Med. 2009. PMID: 19535795 Free article.
Osmotic stress regulates mineralocorticoid receptor expression in a novel aldosterone-sensitive cortical collecting duct cell line.
Viengchareun S, Kamenicky P, Teixeira M, Butlen D, Meduri G, Blanchard-Gutton N, Kurschat C, Lanel A, Martinerie L, Sztal-Mazer S, Blot-Chabaud M, Ferrary E, Cherradi N, Lombès M. Viengchareun S, et al. Among authors: lombes m. Mol Endocrinol. 2009 Dec;23(12):1948-62. doi: 10.1210/me.2009-0095. Epub 2009 Oct 21. Mol Endocrinol. 2009. PMID: 19846540 Free PMC article.
[New insights in growth hormone physiology and pathophysiology].
Kamenicky P, Lombès M, Chanson P. Kamenicky P, et al. Among authors: lombes m. Ann Endocrinol (Paris). 2010 Sep;71 Suppl 1:S25-32. doi: 10.1016/S0003-4266(10)70004-4. Ann Endocrinol (Paris). 2010. PMID: 21237327 Review. French.
Two families with normosmic congenital hypogonadotropic hypogonadism and biallelic mutations in KISS1R (KISS1 receptor): clinical evaluation and molecular characterization of a novel mutation.
Brioude F, Bouligand J, Francou B, Fagart J, Roussel R, Viengchareun S, Combettes L, Brailly-Tabard S, Lombès M, Young J, Guiochon-Mantel A. Brioude F, et al. Among authors: lombes m. PLoS One. 2013;8(1):e53896. doi: 10.1371/journal.pone.0053896. Epub 2013 Jan 18. PLoS One. 2013. PMID: 23349759 Free PMC article.
197 results