Sfoglia per Rivista FAMILIAL CANCER
Lynch syndrome with exclusive skin involvement: time to consider a molecular definition?
2019 Vaisfeld, A.; Calicchia, M.; Pomponi, M. G.; Lucci-Cordisco, E.; Reggiani Bonetti, L.; Genuardi, M.
Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation
2019 de Leon, M. P.; Pedroni, M.; Viel, A.; Luppi, C.; Conigliaro, R.; Domati, F.; Rossi, G.; Bonetti, L. R.
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients
2014 Ponti, Giovanni; Pellacani, Giovanni; Ruini, Cristel; Percesepe, Antonio; Longo, Caterina; Mandel, Victor Desmond; Crucianelli, Francesca; Gorelli, Greta; Tomasi, Aldo
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC.
2001 Lucci Cordisco, E.; Ravella, V.; Carrara, S.; Percesepe, Antonio; Pedroni, Monica; Bellacosa, A.; Caluseriu, O.; Fornasarig, M.; Neri, G.; PONZ DE LEON, Maurizio; Viel, A.; Genuardi, M.
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 |
---|---|---|---|
Lynch syndrome with exclusive skin involvement: time to consider a molecular definition? | 1-gen-2019 | Vaisfeld, A.; Calicchia, M.; Pomponi, M. G.; Lucci-Cordisco, E.; Reggiani Bonetti, L.; Genuardi, M. | |
Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation | 1-gen-2019 | de Leon, M. P.; Pedroni, M.; Viel, A.; Luppi, C.; Conigliaro, R.; Domati, F.; Rossi, G.; Bonetti, L. R. | |
Muir-Torre syndrome or phenocopy? The value of the immunohistochemical expression of mismatch repair proteins in sebaceous tumors of immunocompromised patients | 1-gen-2014 | Ponti, Giovanni; Pellacani, Giovanni; Ruini, Cristel; Percesepe, Antonio; Longo, Caterina; Mandel, Victor Desmond; Crucianelli, Francesca; Gorelli, Greta; Tomasi, Aldo | |
Mutations of the minor mismatch repair gene MSH6 in typical and atypical HNPCC. | 1-gen-2001 | Lucci Cordisco, E.; Ravella, V.; Carrara, S.; Percesepe, Antonio; Pedroni, Monica; Bellacosa, A.; Caluseriu, O.; Fornasarig, M.; Neri, G.; PONZ DE LEON, Maurizio; Viel, A.; Genuardi, M. | |
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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