Viel A - Search Results

1

Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion.

Pastrello C, Baglioni S, Tibiletti MG, Papi L, Fornasarig M, Morabito A, Agostini M, Genuardi M, Viel A. Pastrello C, et al. Among authors: viel a. Eur J Hum Genet. 2006 Jan;14(1):63-8. doi: 10.1038/sj.ejhg.5201517. Eur J Hum Genet. 2006. PMID: 16251890

2

Hereditary nonpolyposis colorectal cancer: review of clinical, molecular genetics, and counseling aspects.

Bellacosa A, Genuardi M, Anti M, Viel A, Ponz de Leon M. Bellacosa A, et al. Among authors: viel a. Am J Med Genet. 1996 Apr 24;62(4):353-64. doi: 10.1002/(SICI)1096-8628(19960424)62:4<353::AID-AJMG7>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8723065 Review.

3

Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer.

Viel A, Genuardi M, Capozzi E, Leonardi F, Bellacosa A, Paravatou-Petsotas M, Pomponi MG, Fornasarig M, Percesepe A, Roncucci L, Tamassia MG, Benatti P, Ponz de Leon M, Valenti A, Covino M, Anti M, Foletto M, Boiocchi M, Neri G. Viel A, et al. Genes Chromosomes Cancer. 1997 Jan;18(1):8-18. doi: 10.1002/(sici)1098-2264(199701)18:1<8::aid-gcc2>3.0.co;2-7. Genes Chromosomes Cancer. 1997. PMID: 8993976

4

Survival analysis in families affected by hereditary non-polyposis colorectal cancer.

Percesepe A, Benatti P, Roncucci L, Sassatelli R, Fante R, Ganazzi D, Bellacosa A, Genuardi M, Neri G, Viel A, Ponz de Leon M. Percesepe A, et al. Among authors: viel a. Int J Cancer. 1997 May 2;71(3):373-6. doi: 10.1002/(sici)1097-0215(19970502)71:3<373::aid-ijc12>3.0.co;2-h. Int J Cancer. 1997. PMID: 9139871

5

Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility.

Genuardi M, Viel A, Bonora D, Capozzi E, Bellacosa A, Leonardi F, Valle R, Ventura A, Pedroni M, Boiocchi M, Neri G. Genuardi M, et al. Among authors: viel a. Hum Genet. 1998 Jan;102(1):15-20. doi: 10.1007/s004390050648. Hum Genet. 1998. PMID: 9490293

6

MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer.

Genuardi M, Anti M, Capozzi E, Leonardi F, Fornasarig M, Novella E, Bellacosa A, Valenti A, Gasbarrini GB, Roncucci L, Benatti P, Percesepe A, Ponz de Leòn M, Coco C, de Paoli A, Valentini M, Boiocchi M, Neri G, Viel A. Genuardi M, et al. Among authors: viel a. Int J Cancer. 1998 Mar 16;75(6):835-9. doi: 10.1002/(sici)1097-0215(19980316)75:6<835::aid-ijc4>3.0.co;2-w. Int J Cancer. 1998. PMID: 9506527

7

Lack of PMS2 gene-truncating mutations in patients with hereditary colorectal cancer.

Viel A, Novella E, Genuardi M, Capozzi E, Fornasarig M, Pedroni M, Santarosa M, De Leon MP, Della Puppa L, Anti M, Boiocchi M. Viel A, et al. Int J Oncol. 1998 Sep;13(3):565-9. doi: 10.3892/ijo.13.3.565. Int J Oncol. 1998. PMID: 9683794

8

Low incidence of BRCA1 mutations among Italian families with breast and ovarian cancer.

Santarosa M, Viel A, Dolcetti R, Crivellari D, Magri MD, Pizzichetta MA, Tibiletti MG, Gallo A, Tumolo S, Del Tin L, Boiocchi M. Santarosa M, et al. Among authors: viel a. Int J Cancer. 1998 Nov 23;78(5):581-6. doi: 10.1002/(sici)1097-0215(19981123)78:5<581::aid-ijc9>3.0.co;2-g. Int J Cancer. 1998. PMID: 9808526

9

Small bowel carcinoma in hereditary nonpolyposis colorectal cancer.

Benatti P, Roncucci L, Percesepe A, Viel A, Pedroni M, Tamassia MG, Vaccina F, Fante R, De Pietri S, Ponz de Leon M. Benatti P, et al. Among authors: viel a. Am J Gastroenterol. 1998 Nov;93(11):2219-22. doi: 10.1111/j.1572-0241.1998.00618.x. Am J Gastroenterol. 1998. PMID: 9820400

10

High prevalence of activated intraepithelial cytotoxic T lymphocytes and increased neoplastic cell apoptosis in colorectal carcinomas with microsatellite instability.

Dolcetti R, Viel A, Doglioni C, Russo A, Guidoboni M, Capozzi E, Vecchiato N, Macrì E, Fornasarig M, Boiocchi M. Dolcetti R, et al. Among authors: viel a. Am J Pathol. 1999 Jun;154(6):1805-13. doi: 10.1016/S0002-9440(10)65436-3. Am J Pathol. 1999. PMID: 10362805 Free PMC article.

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