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Thyroid Hormone Hyposensitivity: From Genotype to Phenotype and Back.
Rurale G, Di Cicco E, Dentice M, Salvatore D, Persani L, Marelli F, Luongo C. Rurale G, et al. Among authors: marelli f. Front Endocrinol (Lausanne). 2020 Jan 24;10:912. doi: 10.3389/fendo.2019.00912. eCollection 2019. Front Endocrinol (Lausanne). 2020. PMID: 32038483 Free PMC article. Review.
Syndromes of resistance to TSH.
Persani L, Gelmini G, Marelli F, Beck-Peccoz P, Bonomi M. Persani L, et al. Among authors: marelli f. Ann Endocrinol (Paris). 2011 Apr;72(2):60-3. doi: 10.1016/j.ando.2011.03.007. Epub 2011 Apr 21. Ann Endocrinol (Paris). 2011. PMID: 21513912 Review.
Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemia.
Calebiro D, Gelmini G, Cordella D, Bonomi M, Winkler F, Biebermann H, de Marco A, Marelli F, Libri DV, Antonica F, Vigone MC, Cappa M, Mian C, Sartorio A, Beck-Peccoz P, Radetti G, Weber G, Persani L. Calebiro D, et al. Among authors: marelli f. J Clin Endocrinol Metab. 2012 Jan;97(1):E156-60. doi: 10.1210/jc.2011-1938. Epub 2011 Nov 2. J Clin Endocrinol Metab. 2012. PMID: 22049173
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects.
de Filippis T, Marelli F, Nebbia G, Porazzi P, Corbetta S, Fugazzola L, Gastaldi R, Vigone MC, Biffanti R, Frizziero D, Mandarà L, Prontera P, Salerno M, Maghnie M, Tiso N, Radetti G, Weber G, Persani L. de Filippis T, et al. Among authors: marelli f. J Clin Endocrinol Metab. 2016 Mar;101(3):861-70. doi: 10.1210/jc.2015-3403. Epub 2016 Jan 13. J Clin Endocrinol Metab. 2016. PMID: 26760175 Free article.
58 results