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160 results
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Fetal microchimerism as an explanation of disease.
Fugazzola L, Cirello V, Beck-Peccoz P. Fugazzola L, et al. Nat Rev Endocrinol. 2011 Feb;7(2):89-97. doi: 10.1038/nrendo.2010.216. Epub 2010 Dec 21. Nat Rev Endocrinol. 2011. PMID: 21178998 Review.
BRAF V600E status may facilitate decision-making on active surveillance of low-risk papillary thyroid microcarcinoma.
Kim KJ, Kim SG, Tan J, Shen X, Viola D, Elisei R, Puxeddu E, Fugazzola L, Colombo C, Jarzab B, Czarniecka A, Lam AK, Mian C, Vianello F, Yip L, Riesco-Eizaguirre G, Santisteban P, O'Neill CJ, Sywak MS, Clifton-Bligh R, Bendlova B, Sýkorová V, Xing M. Kim KJ, et al. Among authors: fugazzola l. Eur J Cancer. 2020 Jan;124:161-169. doi: 10.1016/j.ejca.2019.10.017. Epub 2019 Nov 29. Eur J Cancer. 2020. PMID: 31790974
Expression of thyrotropin receptor (TSH-R), thyroglobulin, thyroperoxidase, and calcitonin messenger ribonucleic acids in thyroid carcinomas: evidence of TSH-R gene transcript in medullary histotype.
Elisei R, Pinchera A, Romei C, Gryczynska M, Pohl V, Maenhaut C, Fugazzola L, Pacini F. Elisei R, et al. Among authors: fugazzola l. J Clin Endocrinol Metab. 1994 Apr;78(4):867-71. doi: 10.1210/jcem.78.4.8157713. J Clin Endocrinol Metab. 1994. PMID: 8157713
Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.
Fugazzola L, Mannavola D, Cerutti N, Maghnie M, Pagella F, Bianchi P, Weber G, Persani L, Beck-Peccoz P. Fugazzola L, et al. J Clin Endocrinol Metab. 2000 Jul;85(7):2469-75. doi: 10.1210/jcem.85.7.6694. J Clin Endocrinol Metab. 2000. PMID: 10902795 Clinical Trial.
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. J Clin Endocrinol Metab. 2002 Jul;87(7):3201-8. doi: 10.1210/jcem.87.7.8653. J Clin Endocrinol Metab. 2002. PMID: 12107225
Monoallelic expression of mutant thyroid peroxidase allele causing total iodide organification defect.
Fugazzola L, Cerutti N, Mannavola D, Vannucchi G, Fallini C, Persani L, Beck-Peccoz P. Fugazzola L, et al. J Clin Endocrinol Metab. 2003 Jul;88(7):3264-71. doi: 10.1210/jc.2002-021377. J Clin Endocrinol Metab. 2003. PMID: 12843174
Frequent association between MEN 2A and cutaneous lichen amyloidosis.
Verga U, Fugazzola L, Cambiaghi S, Pritelli C, Alessi E, Cortelazzi D, Gangi E, Beck-Peccoz P. Verga U, et al. Among authors: fugazzola l. Clin Endocrinol (Oxf). 2003 Aug;59(2):156-61. doi: 10.1046/j.1365-2265.2003.01782.x. Clin Endocrinol (Oxf). 2003. PMID: 12864791
Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacement.
Fugazzola L, Persani L, Mannavola D, Reschini E, Vannucchi G, Weber G, Beck-Peccoz P. Fugazzola L, et al. Clin Endocrinol (Oxf). 2003 Aug;59(2):230-6. doi: 10.1046/j.1365-2265.2003.01830.x. Clin Endocrinol (Oxf). 2003. PMID: 12864801
BRAF mutations in an Italian cohort of thyroid cancers.
Fugazzola L, Mannavola D, Cirello V, Vannucchi G, Muzza M, Vicentini L, Beck-Peccoz P. Fugazzola L, et al. Clin Endocrinol (Oxf). 2004 Aug;61(2):239-43. doi: 10.1111/j.1365-2265.2004.02089.x. Clin Endocrinol (Oxf). 2004. PMID: 15272920
Different responses to chronic somatostatin analogues in patients with central hyperthyroidism.
Mannavola D, Persani L, Vannucchi G, Zanardelli M, Fugazzola L, Verga U, Facchetti M, Beck-Peccoz P. Mannavola D, et al. Among authors: fugazzola l. Clin Endocrinol (Oxf). 2005 Feb;62(2):176-81. doi: 10.1111/j.1365-2265.2004.02192.x. Clin Endocrinol (Oxf). 2005. PMID: 15670193
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