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Hormonal, Radiological, NP-59 Scintigraphy, and Pathological Correlations in Patients With Cushing's Syndrome Due to Primary Pigmented Nodular Adrenocortical Disease (PPNAD).
Vezzosi D, Tenenbaum F, Cazabat L, Tissier F, Bienvenu M, Carrasco CA, Laloi-Michelin M, Barrande G, Lefebvre H, Hiéronimus S, Tabarin A, Bertagna X, Legmann P, Vantyghem MC, Bertherat J. Vezzosi D, et al. J Clin Endocrinol Metab. 2015 Nov;100(11):4332-8. doi: 10.1210/jc.2015-2174. Epub 2015 Sep 21. J Clin Endocrinol Metab. 2015. PMID: 26390100
Long-term (up to 18 years) effects on GH/IGF-1 hypersecretion and tumour size of primary somatostatin analogue (SSTa) therapy in patients with GH-secreting pituitary adenoma responsive to SSTa.
Maiza JC, Vezzosi D, Matta M, Donadille F, Loubes-Lacroix F, Cournot M, Bennet A, Caron P. Maiza JC, et al. Among authors: vezzosi d. Clin Endocrinol (Oxf). 2007 Aug;67(2):282-9. doi: 10.1111/j.1365-2265.2007.02878.x. Epub 2007 May 24. Clin Endocrinol (Oxf). 2007. PMID: 17524029 Free PMC article. Clinical Trial.
Carney complex: Clinical and genetic 2010 update.
Vezzosi D, Vignaux O, Dupin N, Bertherat J. Vezzosi D, et al. Ann Endocrinol (Paris). 2010 Dec;71(6):486-93. doi: 10.1016/j.ando.2010.08.002. Epub 2010 Sep 17. Ann Endocrinol (Paris). 2010. PMID: 20850710 Review.
Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.
Libé R, Horvath A, Vezzosi D, Fratticci A, Coste J, Perlemoine K, Ragazzon B, Guillaud-Bataille M, Groussin L, Clauser E, Raffin-Sanson ML, Siegel J, Moran J, Drori-Herishanu L, Faucz FR, Lodish M, Nesterova M, Bertagna X, Bertherat J, Stratakis CA. Libé R, et al. Among authors: vezzosi d. J Clin Endocrinol Metab. 2011 Jan;96(1):E208-14. doi: 10.1210/jc.2010-1704. Epub 2010 Nov 3. J Clin Endocrinol Metab. 2011. PMID: 21047926 Free PMC article.
Pathogenesis of benign adrenocortical tumors.
Vezzosi D, Bertherat J, Groussin L. Vezzosi D, et al. Best Pract Res Clin Endocrinol Metab. 2010 Dec;24(6):893-905. doi: 10.1016/j.beem.2010.10.005. Best Pract Res Clin Endocrinol Metab. 2010. PMID: 21115158
Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours.
Rothenbuhler A, Horvath A, Libé R, Faucz FR, Fratticci A, Raffin Sanson ML, Vezzosi D, Azevedo M, Levy I, Almeida MQ, Lodish M, Nesterova M, Bertherat J, Stratakis CA. Rothenbuhler A, et al. Among authors: vezzosi d. Clin Endocrinol (Oxf). 2012 Aug;77(2):195-9. doi: 10.1111/j.1365-2265.2012.04366.x. Clin Endocrinol (Oxf). 2012. PMID: 22335482 Free PMC article.
Phosphodiesterase 11A (PDE11A) gene defects in patients with acth-independent macronodular adrenal hyperplasia (AIMAH): functional variants may contribute to genetic susceptibility of bilateral adrenal tumors.
Vezzosi D, Libé R, Baudry C, Rizk-Rabin M, Horvath A, Levy I, René-Corail F, Ragazzon B, Stratakis CA, Vandecasteele G, Bertherat J. Vezzosi D, et al. J Clin Endocrinol Metab. 2012 Nov;97(11):E2063-9. doi: 10.1210/jc.2012-2275. Epub 2012 Sep 20. J Clin Endocrinol Metab. 2012. PMID: 22996146 Free PMC article.
87 results