MUZZA, MARINA
MUZZA, MARINA
Universita' degli Studi di MILANO
Absence of BRAF mutations in endocrine tumors
2004 D. Mannavola, V. Cirello, M. Muzza, P. Beck-Peccoz, L. Fugazzola
Absence of sonic hedgehog (Shh) germline mutations in patients with thyroid dysgenesis
2008 M. Muzza, L. Persani, T. De Filippis, R. Gastaldi, M.C. Vigone, D. Sala, G. Weber, R. Lorini, P. Beck Peccoz, L. Fugazzola
Absence of sonic hedgehog mutations in a large cohort of children with thyroid dysgenesis
2008 M. Muzza, T. de Filippis, R. Gastaldi, G. Weber, R. Lorini, P. Beck-Peccoz, L. Persani, L. Fugazzola
Allelic distribution of six RET polymorphisms in sporadic medullary thyroid cancer and functional analysis of G691S variant
2006 L. Fugazzola, D. Cordella, V. Cirello, L. Alberti, M. Muzza, P. Beck Peccoz, L. Persani
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyrod carcinoma
2006 D. Cordella, M. Muzza, L. Alberti, P. Colombo, P. Travaglini, P. Beck-Peccoz, L. Fugazzola, L. Persani
An in-frame complex germline mutation in the juxtamembrane intracellular domain causing RET activation in familial medullary thyroid carcinoma
2006 D. Cordella, M. Muzza, L. Alberti, P. Colombo, P. Travaglini, P. Beck Peccoz, L. Fugazzola, L. Persani
An in-frame complex mutation in the juxtamembarne intracellular domain causing RET activation in a familial medullary thyroid carcinoma
2006 L. Fugazzola, D. Cordella, M. Muzza, L. Alberti, P. Travaglini, P. Colombo, P. Beck-Peccoz, L. Persani
Analisi funzionale di una complessa mutazione germinale localizzata nel dominio iuxtamembrana del gene RET in un carcinoma midollare familiare
2005 L. Fugazzola, D. Cordella, M. Muzza, L. Alberti, P. Travaglino, P. Colombo, P. Beck-Peccoz, L. Persani
Analysis of a deiodinase 2 polymorphism (oRFa-Asp) in patients with Graves’ disease and controls : preliminary results
2006 G. Vannucchi, D. Mannavola, V. Cirello, I. Campi, M. Muzza, P. Beck-Peccoz, L. Fugazzola
BRAF mutations in an Italian cohort of thyroid cancers
2004 L. Fugazzola, D. Mannavola, V. Cirello, G. Vannucchi, M. Muzza, L. Vicentini, P.L.M. Beck Peccoz
BRAF mutations in an Italian series of thyroid cancers
2004 L. Fugazzola, D. Mannavola, V. Cirello, G. Vannucchi, M. Muzza, L. Vicentini, P. Beck-Peccoz
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
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
Disorders of H2O2 generation
2017 M. Muzza, L. Fugazzola
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
DUOXS defects : genotype-phenotype correlations
2011 L. Fugazzola, M. Muzza, G. Weber, P. Beck Peccoz, L. Persani
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
Fetal cell microchimerism in papillary thyroid cancer
2007 V. Cirello, M. Muzza, M.P. Recalcati, S. Rossi, M. Perrino, P. Finelli, P. Beck-Peccoz, L. Fugazzola
Fetal cell microchimerism in papillary thyroid cancer
2007 V. Cirello, M. Muzza, P. Recalcati, S. Rossi, M. Perrino, P. Finelli, P. Beck Peccoz, L. Fugazzola
Fetal cell microchimerism in papillary thyroid cancer : a possibile role in tumor demage and tissue repair
2008 V. Cirello, M.P. Recalcati, M. Muzza, S. Rossi, M. Perrino, P. Beck-Peccoz, P. Finelli, L. Fugazzola