Muzza M - Search Results

1

Segregation and expression analyses of hyaluronan-binding protein 2 (HABP2): insights from a large series of familial non-medullary thyroid cancers and literature review.

Colombo C, Muzza M, Proverbio MC, Ercoli G, Perrino M, Cirello V, Vicentini L, Ferrero S, Fugazzola L. Colombo C, et al. Among authors: muzza m. Clin Endocrinol (Oxf). 2017 Jun;86(6):837-844. doi: 10.1111/cen.13316. Epub 2017 Mar 23. Clin Endocrinol (Oxf). 2017. PMID: 28222214

2

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

3

An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma.

Cordella D, Muzza M, Alberti L, Colombo P, Travaglini P, Beck-Peccoz P, Fugazzola L, Persani L. Cordella D, et al. Among authors: muzza m. Endocr Relat Cancer. 2006 Sep;13(3):945-53. doi: 10.1677/erc.1.01144. Endocr Relat Cancer. 2006. PMID: 16954442

4

Histopathological and molecular studies in patients with goiter and hypercalcitoninemia: reactive or neoplastic C-cell hyperplasia?

Verga U, Ferrero S, Vicentini L, Brambilla T, Cirello V, Muzza M, Beck-Peccoz P, Fugazzola L. Verga U, et al. Among authors: muzza m. Endocr Relat Cancer. 2007 Jun;14(2):393-403. doi: 10.1677/ERC-06-0053. Endocr Relat Cancer. 2007. PMID: 17639053

5

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

6

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

7

Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis.

Muzza M, Persani L, de Filippis T, Gastaldi R, Vigone MC, Sala D, Weber G, Lorini R, Beck-Peccoz P, Fugazzola L. Muzza M, et al. Clin Endocrinol (Oxf). 2008 Nov;69(5):828-9. doi: 10.1111/j.1365-2265.2008.03265.x. Epub 2008 Apr 10. Clin Endocrinol (Oxf). 2008. PMID: 18410549 No abstract available.

8

Fetal cell microchimerism in papillary thyroid cancer: a possible role in tumor damage and tissue repair.

Cirello V, Recalcati MP, Muzza M, Rossi S, Perrino M, Vicentini L, Beck-Peccoz P, Finelli P, Fugazzola L. Cirello V, et al. Among authors: muzza m. Cancer Res. 2008 Oct 15;68(20):8482-8. doi: 10.1158/0008-5472.CAN-08-0672. Cancer Res. 2008. PMID: 18922922

9

Fetal cell microchimerism in papillary thyroid cancer: studies in peripheral blood and tissues.

Cirello V, Perrino M, Colombo C, Muzza M, Filopanti M, Vicentini L, Beck-Peccoz P, Fugazzola L. Cirello V, et al. Among authors: muzza m. Int J Cancer. 2010 Jun 15;126(12):2874-8. doi: 10.1002/ijc.24993. Int J Cancer. 2010. PMID: 19856309

10

Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro.

Muzza M, Cordella D, Bombled J, Bressac-de Paillerets B, Guizzardi F, Francis Z, Beck-Peccoz P, Schlumberger M, Persani L, Fugazzola L. Muzza M, et al. Eur J Endocrinol. 2010 Apr;162(4):771-7. doi: 10.1530/EJE-09-0929. Epub 2010 Jan 26. Eur J Endocrinol. 2010. PMID: 20103606

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