Bertario L - Search Results

1

A human cell-based assay to evaluate the effects of alterations in the MLH1 mismatch repair gene.

Blasi MF, Ventura I, Aquilina G, Degan P, Bertario L, Bassi C, Radice P, Bignami M. Blasi MF, et al. Among authors: bertario l. Cancer Res. 2006 Sep 15;66(18):9036-44. doi: 10.1158/0008-5472.CAN-06-1896. Cancer Res. 2006. PMID: 16982745

2

Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes.

Pensotti V, Radice P, Presciuttini S, Calistri D, Gazzoli I, Grimalt Perez A, Mondini P, Buonsanti G, Sala P, Rossetti C, Ranzani GN, Bertario L, Pierotti MA. Pensotti V, et al. Among authors: bertario l. Genes Chromosomes Cancer. 1997 Jul;19(3):135-42. Genes Chromosomes Cancer. 1997. PMID: 9218993

3

Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours.

Giarola M, Wells D, Mondini P, Pilotti S, Sala P, Azzarelli A, Bertario L, Pierotti MA, Delhanty JD, Radice P. Giarola M, et al. Among authors: bertario l. Br J Cancer. 1998 Sep;78(5):582-7. doi: 10.1038/bjc.1998.544. Br J Cancer. 1998. PMID: 9744495 Free PMC article.

4

Rapid assessment of replication error phenotype in gastric cancer.

Buonsanti G, Presciuttini S, Radice P, Pierotti MA, Bertario L, Ranzani GN. Buonsanti G, et al. Among authors: bertario l. Diagn Mol Pathol. 1998 Jun;7(3):168-73. doi: 10.1097/00019606-199806000-00008. Diagn Mol Pathol. 1998. PMID: 9836073

5

Survival of patients with hereditary colorectal cancer: comparison of HNPCC and colorectal cancer in FAP patients with sporadic colorectal cancer.

Bertario L, Russo A, Sala P, Eboli M, Radice P, Presciuttini S, Andreola S, Rodriguez-Bigas MA, Pizzetti P, Spinelli P. Bertario L, et al. Int J Cancer. 1999 Jan 18;80(2):183-7. doi: 10.1002/(sici)1097-0215(19990118)80:2<183::aid-ijc4>3.0.co;2-w. Int J Cancer. 1999. PMID: 9935197

6

Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.

Giarola M, Stagi L, Presciuttini S, Mondini P, Radice MT, Sala P, Pierotti MA, Bertario L, Radice P. Giarola M, et al. Among authors: bertario l. Hum Mutat. 1999;13(2):116-23. doi: 10.1002/(SICI)1098-1004(1999)13:2<116::AID-HUMU3>3.0.CO;2-2. Hum Mutat. 1999. PMID: 10094547

7

Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition.

Calistri D, Presciuttini S, Buonsanti G, Radice P, Gazzoli I, Pensotti V, Sala P, Eboli M, Andreola S, Russo A, Pierotti M, Bertario L, Ranzani GN. Calistri D, et al. Among authors: bertario l. Int J Cancer. 2000 Jan 20;89(1):87-91. doi: 10.1002/(sici)1097-0215(20000120)89:1<87::aid-ijc14>3.0.co;2-9. Int J Cancer. 2000. PMID: 10719736

8

Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis.

Bertario L, Russo A, Sala P, Eboli M, Giarola M, D'amico F, Gismondi V, Varesco L, Pierotti MA, Radice P; Hereditary Colorectal Tumours Registry. Bertario L, et al. Int J Cancer. 2001 Mar 20;95(2):102-7. doi: 10.1002/1097-0215(20010320)95:2<102::aid-ijc1018>3.0.co;2-8. Int J Cancer. 2001. PMID: 11241320

9

Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis.

Bertario L, Russo A, Sala P, Varesco L, Giarola M, Mondini P, Pierotti M, Spinelli P, Radice P; Hereditary Colorectal Tumor Registry. Bertario L, et al. J Clin Oncol. 2003 May 1;21(9):1698-707. doi: 10.1200/JCO.2003.09.118. J Clin Oncol. 2003. PMID: 12721244

10

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.

Gismondi V, Meta M, Bonelli L, Radice P, Sala P, Bertario L, Viel A, Fornasarig M, Arrigoni A, Gentile M, Ponz de Leon M, Anselmi L, Mareni C, Bruzzi P, Varesco L. Gismondi V, et al. Among authors: bertario l. Int J Cancer. 2004 May 1;109(5):680-4. doi: 10.1002/ijc.20054. Int J Cancer. 2004. PMID: 14999774

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