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Page 1
The IGSF1 deficiency syndrome: characteristics of male and female patients.
Joustra SD, Schoenmakers N, Persani L, Campi I, Bonomi M, Radetti G, Beck-Peccoz P, Zhu H, Davis TM, Sun Y, Corssmit EP, Appelman-Dijkstra NM, Heinen CA, Pereira AM, Varewijck AJ, Janssen JA, Endert E, Hennekam RC, Lombardi MP, Mannens MM, Bak B, Bernard DJ, Breuning MH, Chatterjee K, Dattani MT, Oostdijk W, Biermasz NR, Wit JM, van Trotsenburg AS. Joustra SD, et al. Among authors: bonomi m. J Clin Endocrinol Metab. 2013 Dec;98(12):4942-52. doi: 10.1210/jc.2013-2743. Epub 2013 Oct 9. J Clin Endocrinol Metab. 2013. PMID: 24108313
Highly sensitive serum thyroglobulin and circulating thyroglobulin mRNA evaluations in the management of patients with differentiated thyroid cancer in apparent remission.
Fugazzola L, Mihalich A, Persani L, Cerutti N, Reina M, Bonomi M, Ponti E, Mannavola D, Giammona E, Vannucchi G, di Blasio AM, Beck-Peccoz P. Fugazzola L, et al. Among authors: bonomi m. J Clin Endocrinol Metab. 2002 Jul;87(7):3201-8. doi: 10.1210/jcem.87.7.8653. J Clin Endocrinol Metab. 2002. PMID: 12107225
Syndromes of hormone resistance in the hypothalamic-pituitary-thyroid axis.
Beck-Peccoz P, Persani L, Calebiro D, Bonomi M, Mannavola D, Campi I. Beck-Peccoz P, et al. Among authors: bonomi m. Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):529-46. doi: 10.1016/j.beem.2006.11.001. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 17161330 Review.
Genetics and phenomics of hypothyroidism due to TSH resistance.
Persani L, Calebiro D, Cordella D, Weber G, Gelmini G, Libri D, de Filippis T, Bonomi M. Persani L, et al. Among authors: bonomi m. Mol Cell Endocrinol. 2010 Jun 30;322(1-2):72-82. doi: 10.1016/j.mce.2010.01.008. Epub 2010 Jan 18. Mol Cell Endocrinol. 2010. PMID: 20083154 Review.
Syndromes of resistance to TSH.
Persani L, Gelmini G, Marelli F, Beck-Peccoz P, Bonomi M. Persani L, et al. Among authors: bonomi m. 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: bonomi m. 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
304 results