Capella C - Search Results

1

Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.

Agostini M, Tibiletti MG, Lucci-Cordisco E, Chiaravalli A, Morreau H, Furlan D, Boccuto L, Pucciarelli S, Capella C, Boiocchi M, Viel A. Agostini M, et al. Among authors: capella c. Am J Gastroenterol. 2005 Aug;100(8):1886-91. doi: 10.1111/j.1572-0241.2005.50441.x. Am J Gastroenterol. 2005. PMID: 16144131

2

The value of microsatellite instability in the detection of HNPCC families and of sporadic colorectal cancers with special biological features: an investigation on a series of 100 consecutive cases.

Furlan D, Tibiletti MG, Taborelli M, Albarello L, Cornaggia M, Capella C. Furlan D, et al. Among authors: capella c. Ann Oncol. 1998 Aug;9(8):901-6. doi: 10.1023/a:1008307611407. Ann Oncol. 1998. PMID: 9789614 Free article.

3

CHK1 frameshift mutations in genetically unstable colorectal and endometrial cancers.

Bertoni F, Codegoni AM, Furlan D, Tibiletti MG, Capella C, Broggini M. Bertoni F, et al. Among authors: capella c. Genes Chromosomes Cancer. 1999 Oct;26(2):176-80. Genes Chromosomes Cancer. 1999. PMID: 10469457

4

Immunohistochemical pattern of hMSH2/hMLH1 in familial and sporadic colorectal, gastric, endometrial and ovarian carcinomas with instability in microsatellite sequences.

Chiaravalli AM, Furlan D, Facco C, Tibiletti MG, Dionigi A, Casati B, Albarello L, Riva C, Capella C. Chiaravalli AM, et al. Among authors: capella c. Virchows Arch. 2001 Jan;438(1):39-48. doi: 10.1007/s004280000325. Virchows Arch. 2001. PMID: 11213834

5

Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family.

Cerutti R, Sahnane N, Carnevali I, Furlan D, Tibiletti MG, Chiaravalli AM, Capella C. Cerutti R, et al. Among authors: capella c. Fam Cancer. 2010 Sep;9(3):275-82. doi: 10.1007/s10689-009-9315-z. Fam Cancer. 2010. PMID: 20041308

6

Microsatellite instability in endometrial cancer: relation to histological subtypes.

Tibiletti MG, Furlan D, Taborelli M, Facco C, Riva C, Franchi M, Cossu A, Trubia M, Taramelli R, Capella C. Tibiletti MG, et al. Among authors: capella c. Gynecol Oncol. 1999 May;73(2):247-52. doi: 10.1006/gyno.1999.5351. Gynecol Oncol. 1999. PMID: 10329042

7

Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa.

Beghini A, Tibiletti MG, Roversi G, Chiaravalli AM, Serio G, Capella C, Larizza L. Beghini A, et al. Among authors: capella c. Cancer. 2001 Aug 1;92(3):657-62. doi: 10.1002/1097-0142(20010801)92:3<657::aid-cncr1367>3.0.co;2-d. Cancer. 2001. PMID: 11505412

8

Low incidence of hereditary nonpolyposis colorectal cancer syndrome in a selected area of the Lombardy Cancer Registry.

Cornaggia M, Tibiletti MG, Albarello L, Taborelli M, Dalla Longa E, Capella C. Cornaggia M, et al. Among authors: capella c. Tumori. 2000 Nov-Dec;86(6):439-44. doi: 10.1177/030089160008600601. Tumori. 2000. PMID: 11218182

9

Colorectal poorly differentiated neuroendocrine carcinomas and mixed adenoneuroendocrine carcinomas: insights into the diagnostic immunophenotype, assessment of methylation profile, and search for prognostic markers.

La Rosa S, Marando A, Furlan D, Sahnane N, Capella C. La Rosa S, et al. Among authors: capella c. Am J Surg Pathol. 2012 Apr;36(4):601-11. doi: 10.1097/PAS.0b013e318242e21c. Am J Surg Pathol. 2012. PMID: 22314183

10

Pyrosequencing for EGFR mutation detection: diagnostic accuracy and clinical implications.

Sahnane N, Gueli R, Tibiletti MG, Bernasconi B, Stefanoli M, Franzi F, Pinotti G, Capella C, Furlan D. Sahnane N, et al. Among authors: capella c. Diagn Mol Pathol. 2013 Dec;22(4):196-203. doi: 10.1097/PDM.0b013e3182893f55. Diagn Mol Pathol. 2013. PMID: 24193003

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