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Results: 1 to 20 of 141

1.

[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].

Olschwang S, Bonaïti C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F.

Bull Cancer. 2004 Apr;91(4):303-15. Review. French.

PMID:
15242312
[PubMed - indexed for MEDLINE]
2.

[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].

Olschwang S, Bonaïti-Pellié C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F.

Pathol Biol (Paris). 2006 May;54(4):215-29. Epub 2006 May 4. Review. French.

PMID:
16677780
[PubMed - indexed for MEDLINE]
3.

[HNPCC syndrome (hereditary non polyposis colon cancer): identification and management].

Olschwang S, Bonaïti C, Feingold J, Frébourg T, Grandjouan S, Lasset C, Laurent-Puig P, Lecuru F, Millat B, Sobol H, Thomas G, Eisinger F.

Rev Med Interne. 2005 Feb;26(2):109-18. Review. French.

PMID:
15710257
[PubMed - indexed for MEDLINE]
4.

Identification of HNPCC by molecular analysis of colorectal and endometrial tumors.

Vasen HF, Hendriks Y, de Jong AE, van Puijenbroek M, Tops C, Bröcker-Vriends AH, Wijnen JT, Morreau H.

Dis Markers. 2004;20(4-5):207-13. Review.

PMID:
15528786
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Refining the Amsterdam Criteria and Bethesda Guidelines: testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic.

Lipton LR, Johnson V, Cummings C, Fisher S, Risby P, Eftekhar Sadat AT, Cranston T, Izatt L, Sasieni P, Hodgson SV, Thomas HJ, Tomlinson IP.

J Clin Oncol. 2004 Dec 15;22(24):4934-43. Erratum in: J Clin Oncol. 2005 May 20;23(15):3652.

PMID:
15611508
[PubMed - indexed for MEDLINE]
Free Article
6.

Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.

Bonis PA, Trikalinos TA, Chung M, Chew P, Ip S, DeVine DA, Lau J.

Evid Rep Technol Assess (Full Rep). 2007 May;(150):1-180. Review.

PMID:
17764220
[PubMed - indexed for MEDLINE]
Free Article
7.

Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer.

Southey MC, Jenkins MA, Mead L, Whitty J, Trivett M, Tesoriero AA, Smith LD, Jennings K, Grubb G, Royce SG, Walsh MD, Barker MA, Young JP, Jass JR, St John DJ, Macrae FA, Giles GG, Hopper JL.

J Clin Oncol. 2005 Sep 20;23(27):6524-32. Epub 2005 Aug 22.

PMID:
16116158
[PubMed - indexed for MEDLINE]
Free Article
8.

Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium.

Millar AL, Pal T, Madlensky L, Sherman C, Temple L, Mitri A, Cheng H, Marcus V, Gallinger S, Redston M, Bapat B, Narod S.

Hum Mol Genet. 1999 May;8(5):823-9.

PMID:
10196371
[PubMed - indexed for MEDLINE]
Free Article
9.

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree.

Wagner A, Hendriks Y, Meijers-Heijboer EJ, de Leeuw WJ, Morreau H, Hofstra R, Tops C, Bik E, Bröcker-Vriends AH, van Der Meer C, Lindhout D, Vasen HF, Breuning MH, Cornelisse CJ, van Krimpen C, Niermeijer MF, Zwinderman AH, Wijnen J, Fodde R.

J Med Genet. 2001 May;38(5):318-22.

PMID:
11333868
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.

Lagerstedt Robinson K, Liu T, Vandrovcova J, Halvarsson B, Clendenning M, Frebourg T, Papadopoulos N, Kinzler KW, Vogelstein B, Peltomäki P, Kolodner RD, Nilbert M, Lindblom A.

J Natl Cancer Inst. 2007 Feb 21;99(4):291-9.

PMID:
17312306
[PubMed - indexed for MEDLINE]
Free Article
11.

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients.

de Leeuw WJ, Dierssen J, Vasen HF, Wijnen JT, Kenter GG, Meijers-Heijboer H, Brocker-Vriends A, Stormorken A, Moller P, Menko F, Cornelisse CJ, Morreau H.

J Pathol. 2000 Nov;192(3):328-35.

PMID:
11054716
[PubMed - indexed for MEDLINE]
12.

[HNPCC (hereditary non-polyposis colorectal cancer) or Lynch syndrome: a syndrome related to a failure of DNA repair system].

Manceau G, Karoui M, Charachon A, Delchier JC, Sobhani I.

Bull Cancer. 2011 Mar;98(3):323-36. doi: 10.1684/bdc.2011.1328. Review. French.

PMID:
21459714
[PubMed - indexed for MEDLINE]
13.
14.
15.

Distinct PTEN mutational spectra in hereditary non-polyposis colon cancer syndrome-related endometrial carcinomas compared to sporadic microsatellite unstable tumors.

Zhou XP, Kuismanen S, Nystrom-Lahti M, Peltomaki P, Eng C.

Hum Mol Genet. 2002 Feb 15;11(4):445-50.

PMID:
11854177
[PubMed - indexed for MEDLINE]
Free Article
16.

Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features.

Schiemann U, Müller-Koch Y, Gross M, Daum J, Lohse P, Baretton G, Muders M, Mussack T, Kopp R, Holinski-Feder E.

Digestion. 2004;69(3):166-76. Epub 2004 Apr 28.

PMID:
15118395
[PubMed - indexed for MEDLINE]
17.

Microsatellite instability as a predictor of a mutation in a DNA mismatch repair gene in familial colorectal cancer.

Liu T, Wahlberg S, Burek E, Lindblom P, Rubio C, Lindblom A.

Genes Chromosomes Cancer. 2000 Jan;27(1):17-25.

PMID:
10564582
[PubMed - indexed for MEDLINE]
18.

[The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation].

Czakó L, Tiszlavicz L, Takács R, Baradnay G, Lonovics J, Cserni G, Závodná K, Bartosova Z.

Orv Hetil. 2005 May 15;146(20):1009-16. Hungarian.

PMID:
15945244
[PubMed - indexed for MEDLINE]
19.

Correlations between phenotype and microsatellite instability in HNPCC: implications for genetic testing.

Palmirotta R, Matera S, Curia MC, Aceto G, el Zhobi B, Verginelli F, Guadagni F, Casale V, Stigliano V, Messerini L, Mariani-Costantini R, Battista P, Cama A.

Fam Cancer. 2004;3(2):117-21.

PMID:
15340262
[PubMed - indexed for MEDLINE]
20.

Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis.

Berends MJ, Wu Y, Sijmons RH, van der Sluis T, Ek WB, Ligtenberg MJ, Arts NJ, ten Hoor KA, Kleibeuker JH, de Vries EG, Mourits MJ, Hollema H, Buys CH, Hofstra RM, van der Zee AG.

J Clin Oncol. 2003 Dec 1;21(23):4364-70.

PMID:
14645426
[PubMed - indexed for MEDLINE]
Free Article

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