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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: campi i. 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
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: campi i. 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.
New immunomodulators in the treatment of Graves' ophthalmopathy.
Salvi M, Vannucchi G, Campi I, Currò N, Beck-Peccoz P. Salvi M, et al. Among authors: campi i. Ann Endocrinol (Paris). 2008 Apr;69(2):153-6. doi: 10.1016/j.ando.2008.02.013. Epub 2008 Apr 15. Ann Endocrinol (Paris). 2008. PMID: 18417090
Impact of resistance to thyroid hormone on the cardiovascular system in adults.
Pulcrano M, Palmieri EA, Mannavola D, Ciulla M, Campi I, Covelli D, Lombardi G, Biondi B, Beck-Peccoz P. Pulcrano M, et al. Among authors: campi i. J Clin Endocrinol Metab. 2009 Aug;94(8):2812-6. doi: 10.1210/jc.2009-0096. Epub 2009 May 12. J Clin Endocrinol Metab. 2009. PMID: 19435825 Free article.
Pituitary tumours: TSH-secreting adenomas.
Beck-Peccoz P, Persani L, Mannavola D, Campi I. Beck-Peccoz P, et al. Among authors: campi i. Best Pract Res Clin Endocrinol Metab. 2009 Oct;23(5):597-606. doi: 10.1016/j.beem.2009.05.006. Best Pract Res Clin Endocrinol Metab. 2009. PMID: 19945025 Review.
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement.
Sun Y, Bak B, Schoenmakers N, van Trotsenburg AS, Oostdijk W, Voshol P, Cambridge E, White JK, le Tissier P, Gharavy SN, Martinez-Barbera JP, Stokvis-Brantsma WH, Vulsma T, Kempers MJ, Persani L, Campi I, Bonomi M, Beck-Peccoz P, Zhu H, Davis TM, Hokken-Koelega AC, Del Blanco DG, Rangasami JJ, Ruivenkamp CA, Laros JF, Kriek M, Kant SG, Bosch CA, Biermasz NR, Appelman-Dijkstra NM, Corssmit EP, Hovens GC, Pereira AM, den Dunnen JT, Wade MG, Breuning MH, Hennekam RC, Chatterjee K, Dattani MT, Wit JM, Bernard DJ. Sun Y, et al. Among authors: campi i. Nat Genet. 2012 Dec;44(12):1375-81. doi: 10.1038/ng.2453. Epub 2012 Nov 11. Nat Genet. 2012. PMID: 23143598 Free PMC article.
A novel albumin gene mutation (R222I) in familial dysalbuminemic hyperthyroxinemia.
Schoenmakers N, Moran C, Campi I, Agostini M, Bacon O, Rajanayagam O, Schwabe J, Bradbury S, Barrett T, Geoghegan F, Druce M, Beck-Peccoz P, O'Toole A, Clark P, Bignell M, Lyons G, Halsall D, Gurnell M, Chatterjee K. Schoenmakers N, et al. Among authors: campi i. J Clin Endocrinol Metab. 2014 Jul;99(7):E1381-6. doi: 10.1210/jc.2013-4077. Epub 2014 Mar 19. J Clin Endocrinol Metab. 2014. PMID: 24646103 Free PMC article.
60 results