POGLIAGHI, GABRIELE
POGLIAGHI, GABRIELE
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Clinical and Genetic Features of a Large Monocentric Series of Familial Non-Medullary Thyroid Cancers
2021 V. Cirello, C. Colombo, O. Karapanou, G. Pogliaghi, 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
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
Genetic variants of PARP4 gene and PARP4P2 pseudogene in patients with multiple primary tumors including thyroid cancer.
2019 V. Cirello, C. Colombo, G. Pogliaghi, M. Proverbio, S. Rossi, E. Mussani, D. Tosi, G. Bulfamante, E. Bonoldi, G. Gherardi, L. Persani, L. Fugazzola
Intratumoral genetic heterogeneity in papillary thyroid cancer : Occurrence and clinical significance
2020 L. Fugazzola, M. Muzza, G. Pogliaghi, M. Vitale
Molecular markers for the classification of cytologically indeterminate thyroid nodules.
2019 M. Muzza, C. Colombo, G. Pogliaghi, O. Karapanou, 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
The molecular and gene/miRNA expression profiles of radioiodine resistant papillary thyroid cancer
2020 C. Colombo, E. Minna, C. Gargiuli, M. Muzza, M. Dugo, L. De Cecco, G. Pogliaghi, D. Tosi, G. Bulfamante, A. Greco, L. Fugazzola, M. Borrello
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
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
Triple-A Syndrome (TAS): an in-depth overview on genetic and phenotype heterogeneity
2020 G. Pogliaghi, B. Cangiano, P. Duminuco, V. Vezzoli, M. Bonomi
Two novel truncating variants of the AAAS gene causative of the triple A syndrome
2020 V. Vezzoli, P. Duminuco, G. Pogliaghi, M. Saccone, B. Cangiano, M.C. Rosatelli, A. Meloni, L. Persani, M. Bonomi