Sfoglia per Rivista  FAMILIAL CANCER

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Mostrati risultati da 1 a 16 di 16
Titolo Data di pubblicazione Autore(i) File
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome. 1-gen-2012 Ponti, Giovanni; L., Pastorino; A., Pollio; S., Nasti; Pellacani, Giovanni; M. D., Mignogna; Tomasi, Aldo; C. D., Forno; Longo, Caterina; G., Bianchi Scarrà; G., Ficarra; Seidenari, Stefania
Analysis of mismatch repair gene mutations in Turkish HNPCC patients. 1-gen-2010 Berrin, Tunca; Pedroni, Monica; Gulsah, Cecener; Unal, Egeli; Enrica, Borsi; Abdullah, Zorluoglu; Carmela Di, Gregorio; Tuncay, Yilmazlar; Omaer, Yerci; PONZ DE LEON, Maurizio
Attenuated polyposis of the large bowel: a morphologic and molecular approach 1-gen-2017 PONZ DE LEON, Maurizio; Pedroni, Monica; Roncucci, Luca; Domati, Federica; Rossi, Giuseppina; Magnani, Giulia; Pezzi, Annalisa; Fante, Rossella; Bonetti, Luca Reggiani
A case of pneumatosis cystoides intestinalis mimicking familial adenomatous polyposis. 1-gen-2013 PONZ DE LEON, Maurizio; Bertarelli, C; Casadei, Gp; Grilli, A; Bacchini, P; Pedroni, Monica; Jovine, E.
Different involvement of target genes mutations in hereditary and sporadic colorectal cancer with Microsatellite Instability. 1-gen-2003 Borghi, F; Pedroni, Monica; Lamberti, I; Menigatti, M; Ponti, Giovanni; Rossi, G; Di Gregorio, C; Losi, Lorena; Scarselli, A; Benatti, P; Roncucci, Luca; PONZ DE LEON, Maurizio
Identification and biomolecular characterization of Muir-Torre Syndrome 1-gen-2003 Ponti, Giovanni; Roncucci, Luca; Di Gregorio, C; Pedroni, Monica; Borghi, F; Lamberti, I; Rossi, G; Abbati, G; Scarselli, A; Riegler, G; Seidenari, S; Pellacani, Giovanni; Lembo, L; Benatti, P; PONZ DE LEON, Maurizio
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
Mostrati risultati da 1 a 16 di 16
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