MUZZA, MARINA
MUZZA, MARINA
Universita' degli Studi di MILANO
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism
2023 D. Gentilini, M. Muzza, T. de Filippis, M.C. Vigone, G. Weber, L. Calzari, A. Cassio, M. Di Frenna, M. Bartolucci, E.S. Grassi, E. Carbone, A. Olivieri, L. Persani
Thyroid cancer harboring PTEN and TP53 mutations: A peculiar molecular and clinical case report
2022 C. Colombo, G. Pogliaghi, D. Tosi, M. Muzza, G. Bulfamante, L. Persani, L. Fugazzola, V. Cirello
FAM83B is involved in thyroid cancer cell differentiation and migration
2022 V. Cirello, E. Grassi, G. Pogliaghi, V. Ghiandai, L. Ermellino, M. Muzza, G. Gazzano, L. Persani, C. Colombo, L. Fugazzola
Oxidative Stress Correlates with More Aggressive Features in Thyroid Cancer
2022 M. Muzza, G. Pogliaghi, C. Colombo, E. Carbone, V. Cirello, S. Palazzo, F. Frattini, D. Gentilini, G. Gazzano, L. Persani, L. Fugazzola
Combined Mutational and Clonality Analyses Support the Existence of Intra-Tumor Heterogeneity in Papillary Thyroid Cancer
2021 M. Muzza, G. Pogliaghi, L. Persani, L. Fugazzola, C. Colombo
The thyroid risk score (TRS) for nodules with indeterminate cytology
2021 C. Colombo, M. Muzza, G. Pogliaghi, S. Palazzo, G. Vannucchi, L. Vicentini, L. Persani, G. Gazzano, L. Fugazzola
New genetics in congenital hypothyroidism
2021 A. Stoupa, D. Kariyawasam, M. Muzza, T. de Filippis, L. Fugazzola, M. Polak, L. Persani, A. Carre
DUOX2/DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom
2019 C. Peters, A. Nicholas, E. Schoenmakers, G. Lyons, S. Langham, E. Serra, N. Sebire, M. Muzza, L. Fugazzola, N. Schoenmakers
The BRAF-inhibitor PLX4720 inhibits CXCL8 secretion in BRAFV600E mutated and normal thyroid cells : a further anti-cancer effect of BRAF-inhibitors
2019 F. Coperchini, L. Croce, M. Denegri, O. Awwad, S.T. Ngnitejeu, M. Muzza, V. Capelli, F. Latrofa, L. Persani, L. Chiovato, M. Rotondi
Impact of Mutation Density and Heterogeneity on Papillary Thyroid Cancer Clinical Features and Remission Probability
2019 C. Colombo, M. Muzza, M.C. Proverbio, D. Tosi, D. Soranna, C. Pesenti, S. Rossi, V. Cirello, S. De Leo, N. Fusco, M. Miozzo, G. Bulfamante, L. Vicentini, S. Ferrero, A. Zambon, S. Tabano, L. Fugazzola
Genetics and management of congenital hypothyroidism
2018 L. Persani, G. Rurale, T. de Filippis, E. Galazzi, M. Muzza, L. Fugazzola
Letter regarding the article: "Multiple HABP2 variants in familial papillary thyroid carcinoma: Contribution of a group of "thyroid-checked" controls" by Kern et al
2018 C. Colombo, L. Fugazzola, M. Muzza, M. Proverbio, V. Cirello
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma : the PTC-MA assay
2018 C. Pesenti, M. Muzza, C. Colombo, M.C. Proverbio, C. Faré, S. Ferrero, M. Miozzo, L. Fugazzola, S. Tabano
Segregation and expression analyses of hyaluronan-binding protein 2 (HABP2) : insights from a large series of familial non-medullary thyroid cancers and literature review
2017 C. Colombo, M. Muzza, M. Proverbio, G. Ercoli, M. Perrino, V. Cirello, L. Vicentini, S. Ferrero, L. Fugazzola
Disorders of H2O2 generation
2017 M. Muzza, L. Fugazzola
Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism
2017 Z. Aycan, H. Cangul, M. Muzza, V. Bas, L. Fugazzola, V. Chatterjee, L. Persani, N. Schoenmakers
Retinal photoreceptor functions are compromised in patients with resistance to thyroid hormone syndrome (RTHβ)
2017 I. Campi, G. Cammarata, S. Bianchi Marzoli, P. Beck-Peccoz, D. Santarsiero, D. Dazzi, A. Bottari de Castello, E.G. Taroni, F. Viola, C. Mian, S. Watuntantrige Fernando, C. Pelusi, M. Muzza, M.A. Maffini, L. Persani
Oxidative stress and the subcellular localization of the telomerase reverse transcriptase (TERT) in papillary thyroid cancer
2016 M. Muzza, C. Colombo, V. Cirello, M. Perrino, L. Vicentini, L. Fugazzola
Fetal cell microchimerism in papillary thyroid cancer : a role in the outcome of the disease
2015 V. Cirello, C. Colombo, M. Perrino, S. De Leo, M. Muzza, M.A. Maffini, L. Fugazzola
Telomerase in differentiated thyroid cancer : promoter mutations, expression and localization
2015 M. Muzza, C. Colombo, S. Rossi, D. Tosi, V. Cirello, M. Perrino, S. De Leo, E. Magnani, E. Pignatti, B. Vigo, M. Simoni, G. Bulfamante, L. Vicentini, L. Fugazzola