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Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.
De Marco G, Agretti P, Montanelli L, Di Cosmo C, Bagattini B, De Servi M, Ferrarini E, Dimida A, Freitas Ferreira AC, Molinaro A, Ceccarelli C, Brozzi F, Pinchera A, Vitti P, Tonacchera M. De Marco G, et al. Among authors: bagattini b. J Clin Endocrinol Metab. 2011 Aug;96(8):E1335-9. doi: 10.1210/jc.2010-2467. Epub 2011 May 11. J Clin Endocrinol Metab. 2011. PMID: 21565790
Gene expression profile in functioning and non-functioning nodules of autonomous multinodular goiter from an area of iodine deficiency: unexpected common characteristics between the two entities.
Agretti P, De Marco G, Ferrarini E, Di Cosmo C, Montanelli L, Bagattini B, Chiovato L, Tonacchera M. Agretti P, et al. Among authors: bagattini b. J Endocrinol Invest. 2022 Feb;45(2):399-411. doi: 10.1007/s40618-021-01660-y. Epub 2021 Aug 17. J Endocrinol Invest. 2022. PMID: 34405392 Free PMC article.
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