GIRONI, LAURA CRISTINA
GIRONI, LAURA CRISTINA
SCIENZE MEDICHE
CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma
2016-01-01 Betti, M; Aspesi, A; Biasi, A; Casalone, E; Ferrante, D; Ogliara, P; Gironi, Lc; Giorgione, R; Farinelli, P; Grosso, F; Libener, R; Rosato, S; Turchetti, D; Maffè, A; Casadio, C; Ascoli, V; Dianzani, C; Colombo, E; Piccolini, E; Pavesi, M; Miccoli, S; Mirabelli, D; Bracco, C; Righi, L; Boldorini, R; Papotti, M; Matullo, G; Magnani, C; Pasini, B; Dianzani, I
Concordance of p16, FH, and alpha-SMA expression with the fumarate hydratase gene mutational status in sporadic and hereditary piloleiomyomas.
2019-01-01 Gironi L.C.; Camillo L.; Zottarelli F.; Farinelli P.; Spina P.; Dianzani I.; Boldorini R.L.; Valente G.; Colombo E.; Pasini B.; Ogliara P.; Restivo F.; Savoia P.
Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism
2019-01-01 Gironi, Laura Cristina; Colombo, Enrico; Brusco, Alfredo; Grosso, Enrico; Naretto, Valeria Giorgia; Guala, Andrea; Di Gregorio, Eleonora; Zonta, Andrea; Zottarelli, Francesca; Pasini, Barbara; Savoia, Paola
Germline CDKN2A mutations in childhood melanoma: A case of melanoma-pancreatic cancer syndrome
2015-01-01 Gironi, Laura Cristina; Colombo, Enrico; Farinelli, Pamela; Giorgione, Roberto; Bozzola, Cristina; Ogliara, Paola; Pasini, Barbara
Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers
2018-01-01 Gironi, Laura Cristina; Colombo, Enrico; Pasini, Barbara; Giorgione, Roberto; Farinelli, Pamela; Zottarelli, Francesca; Esposto, Elia; Zavattaro, Elisa; Allara, Elias; Ogliara, Paola; Betti, Marta; Dianzani, Irma; Savoia, Paola
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma | 2016 | Betti, M; Aspesi, A; Biasi, A; Casalone, E; Ferrante, D; Ogliara, P; Gironi, Lc; Giorgione, R; Farinelli, P; Grosso, F; Libener, R; Rosato, S; Turchetti, D; Maffè, A; Casadio, C; Ascoli, V; Dianzani, C; Colombo, E; Piccolini, E; Pavesi, M; Miccoli, S; Mirabelli, D; Bracco, C; Righi, L; Boldorini, R; Papotti, M; Matullo, G; Magnani, C; Pasini, B; Dianzani, I | |
| Concordance of p16, FH, and alpha-SMA expression with the fumarate hydratase gene mutational status in sporadic and hereditary piloleiomyomas. | 2019 | Gironi L.C.; Camillo L.; Zottarelli F.; Farinelli P.; Spina P.; Dianzani I.; Boldorini R.L.; Valente G.; Colombo E.; Pasini B.; Ogliara P.; Restivo F.; Savoia P. | |
| Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism | 2019 | Gironi, Laura Cristina; Colombo, Enrico; Brusco, Alfredo; Grosso, Enrico; Naretto, Valeria Giorgia; Guala, Andrea; Di Gregorio, Eleonora; Zonta, Andrea; Zottarelli, Francesca; Pasini, Barbara; Savoia, Paola | |
| Germline CDKN2A mutations in childhood melanoma: A case of melanoma-pancreatic cancer syndrome | 2015 | Gironi, Laura Cristina; Colombo, Enrico; Farinelli, Pamela; Giorgione, Roberto; Bozzola, Cristina; Ogliara, Paola; Pasini, Barbara | |
| Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers | 2018 | Gironi, Laura Cristina; Colombo, Enrico; Pasini, Barbara; Giorgione, Roberto; Farinelli, Pamela; Zottarelli, Francesca; Esposto, Elia; Zavattaro, Elisa; Allara, Elias; Ogliara, Paola; Betti, Marta; Dianzani, Irma; Savoia, Paola |