Sfoglia per Rivista FAMILIAL CANCER
Primary fallopian tube carcinoma (PFTC) in a BRIP-1 mutation carrier: the first case report
2020 Grandi, G.; Caroli, M.; Alboni, C.; Cortesi, L.; Toss, A.; Barbieri, E.; Botticelli, L.; Facchinetti, F.
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe
2010 Vasen, Hf; Möslein, G; Alonso, A; Aretz, S; Bernstein, I; Bertario, L; Blanco, I; Bulow, S; Burn, J; Capella, G; Colas, C; Engel, C; Frayling, I; Rahner, N; Hes, Fj; Hodgson, S; Mecklin, Jp; Møller, P; Myrhøj, T; Nagengast, Fm; Parc, Y; PONZ DE LEON, Maurizio; Renkonen Sinisalo, L; Sampson, Jr; Stormorken, A; Tejpar, S; Thomas, Hj; Wijnen, J; Lubinski, J; Järvinen, H; Claes, E; Heinimann, K; Karagiannis, Ja; Lindblom, A; Dove Edwin, I; Müller, H.
Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation.
2010 Bouzourene, H; Hutter, P; Losi, Lorena; Martin, P; Benhattar, J.
Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment.
2012 L., Belvederesi; F., Bianchi; C., Loretelli; R., Bracci; Cascinu, Stefano; R., Cellerino
The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) - Results of an international collaborative study
2001 M. u. l. l. e. r. W., Burgart; Lj, ; Krause Paulus, R.; PONZ DE LEON, Maurizio
An unusual case of familial adenomatous polyposis with very early symptom occurrence
2014 PONZ DE LEON, Maurizio; Bianchini, Maria Anastasia; REGGIANI BONETTI, Luca; Pedroni, Monica; Di Gregorio, Carmela; Merighi, Alberto; Rossi, Giuseppina; Magnani, Giulia; Domati, Federica; Cacciari, Alfredo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Primary fallopian tube carcinoma (PFTC) in a BRIP-1 mutation carrier: the first case report | 1-gen-2020 | Grandi, G.; Caroli, M.; Alboni, C.; Cortesi, L.; Toss, A.; Barbieri, E.; Botticelli, L.; Facchinetti, F. | |
| Recommendations to improve identification of hereditary and familial colorectal cancer in Europe | 1-gen-2010 | Vasen, Hf; Möslein, G; Alonso, A; Aretz, S; Bernstein, I; Bertario, L; Blanco, I; Bulow, S; Burn, J; Capella, G; Colas, C; Engel, C; Frayling, I; Rahner, N; Hes, Fj; Hodgson, S; Mecklin, Jp; Møller, P; Myrhøj, T; Nagengast, Fm; Parc, Y; PONZ DE LEON, Maurizio; Renkonen Sinisalo, L; Sampson, Jr; Stormorken, A; Tejpar, S; Thomas, Hj; Wijnen, J; Lubinski, J; Järvinen, H; Claes, E; Heinimann, K; Karagiannis, Ja; Lindblom, A; Dove Edwin, I; Müller, H. | |
| Selection of patients with germline MLH1 mutated Lynch syndrome by determination of MLH1 methylation and BRAF mutation. | 1-gen-2010 | Bouzourene, H; Hutter, P; Losi, Lorena; Martin, P; Benhattar, J. | |
| Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment. | 1-gen-2012 | L., Belvederesi; F., Bianchi; C., Loretelli; R., Bracci; Cascinu, Stefano; R., Cellerino | |
| The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) - Results of an international collaborative study | 1-gen-2001 | M. u. l. l. e. r. W., Burgart; Lj, ; Krause Paulus, R.; PONZ DE LEON, Maurizio | |
| An unusual case of familial adenomatous polyposis with very early symptom occurrence | 1-gen-2014 | PONZ DE LEON, Maurizio; Bianchini, Maria Anastasia; REGGIANI BONETTI, Luca; Pedroni, Monica; Di Gregorio, Carmela; Merighi, Alberto; Rossi, Giuseppina; Magnani, Giulia; Domati, Federica; Cacciari, Alfredo |
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