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Page 1
New genetics in congenital hypothyroidism.
Stoupa A, Kariyawasam D, Muzza M, de Filippis T, Fugazzola L, Polak M, Persani L, Carré A. Stoupa A, et al. Among authors: muzza m. Endocrine. 2021 Mar;71(3):696-705. doi: 10.1007/s12020-021-02646-9. Epub 2021 Mar 1. Endocrine. 2021. PMID: 33650047 Review.
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. Among authors: muzza m. Clin Endocrinol (Oxf). 2004 Aug;61(2):239-43. doi: 10.1111/j.1365-2265.2004.02089.x. Clin Endocrinol (Oxf). 2004. PMID: 15272920
High phenotypic intrafamilial variability in patients with Pendred syndrome and a novel duplication in the SLC26A4 gene: clinical characterization and functional studies of the mutated SLC26A4 protein.
Fugazzola L, Cirello V, Dossena S, Rodighiero S, Muzza M, Castorina P, Lalatta F, Ambrosetti U, Beck-Peccoz P, Bottà G, Paulmichl M. Fugazzola L, et al. Among authors: muzza m. Eur J Endocrinol. 2007 Sep;157(3):331-8. doi: 10.1530/EJE-07-0263. Eur J Endocrinol. 2007. PMID: 17766716
RET genotypes in sporadic medullary thyroid cancer: studies in a large Italian series.
Fugazzola L, Muzza M, Mian C, Cordella D, Barollo S, Alberti L, Cirello V, Dazzi D, Girelli ME, Opocher G, Beck-Peccoz P, Persani L. Fugazzola L, et al. Among authors: muzza m. Clin Endocrinol (Oxf). 2008 Sep;69(3):418-25. doi: 10.1111/j.1365-2265.2008.03218.x. Epub 2008 Feb 11. Clin Endocrinol (Oxf). 2008. PMID: 18284634
44 results