CASALIS, guido claudio
CASALIS, guido claudio
SCIENZE MEDICHE
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns
2014-01-01 Iolanda Borelli;Guido C. Casalis Cavalchini;Serena Del Peschio;Monica Micheletti;Tiziana Venesio;Ivana Sarotto;Anna Allavena;Luisa Delsedime;Marco A. Barberis;Giorgia Mandrile;Paola Berchialla;Paola Ogliara;Cecilia Bracco;Barbara Pasini
A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin
2013-01-01 I. Borelli; M.A. Barberis; F. Spina; G.C. Casalis Cavalchini; C. Vivanet; L. Balestrino; M. Micheletti; A. Allavena; P. Sala; C. Carcassi; B. Pasini
Bi-allelic MSH6 mutations in a case of early onset multiple primary tumors resembling Lynch and Turcot syndrome
2014-01-01 G. C. Casalis Cavalchini; D. Giachino; G. Mandrile; I. Borelli; M. Micheletti; T. Venesio; M. De Marchi; B. Pasini
Fattori genetici predisponenti al carcinoma della mammella
2012-01-01 Pasini B; Vignolo Lutati F; Casalis Cavalchini G; Allavena A; Ogliara P; Bracco C
The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum
2023-01-01 Di Feo, Maria Francesca; Lillback, Victoria; Jokela, Manu; McEntagart, Meriel; Homfray, Tessa; Giorgio, Elisa; Casalis Cavalchini, Guido C; Brusco, Alfredo; Iascone, Maria; Spaccini, Luigina; D'Oria, Patrizia; Savarese, Marco; Udd, Bjarne
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns | 2014 | Iolanda Borelli;Guido C. Casalis Cavalchini;Serena Del Peschio;Monica Micheletti;Tiziana Venesio;Ivana Sarotto;Anna Allavena;Luisa Delsedime;Marco A. Barberis;Giorgia Mandrile;Paola Berchialla;Paola Ogliara;Cecilia Bracco;Barbara Pasini | |
| A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin | 2013 | I. Borelli; M.A. Barberis; F. Spina; G.C. Casalis Cavalchini; C. Vivanet; L. Balestrino; M. Micheletti; A. Allavena; P. Sala; C. Carcassi; B. Pasini | |
| Bi-allelic MSH6 mutations in a case of early onset multiple primary tumors resembling Lynch and Turcot syndrome | 2014 | G. C. Casalis Cavalchini; D. Giachino; G. Mandrile; I. Borelli; M. Micheletti; T. Venesio; M. De Marchi; B. Pasini | |
| Fattori genetici predisponenti al carcinoma della mammella | 2012 | Pasini B; Vignolo Lutati F; Casalis Cavalchini G; Allavena A; Ogliara P; Bracco C | |
| The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum | 2023 | Di Feo, Maria Francesca; Lillback, Victoria; Jokela, Manu; McEntagart, Meriel; Homfray, Tessa; Giorgio, Elisa; Casalis Cavalchini, Guido C; Brusco, Alfredo; Iascone, Maria; Spaccini, Luigina; D'Oria, Patrizia; Savarese, Marco; Udd, Bjarne |