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Items: 1 to 20 of 141

1.

Tobacco use and increased colorectal cancer risk in patients with hereditary nonpolyposis colorectal cancer (Lynch syndrome).

Watson P, Ashwathnarayan R, Lynch HT, Roy HK.

Arch Intern Med. 2004 Dec 13-27;164(22):2429-31.

PMID:
15596632
2.

hMLH1 and hMSH2 gene mutation in Brazilian families with suspected hereditary nonpolyposis colorectal cancer.

Rossi BM, Lopes A, Oliveira Ferreira F, Nakagawa WT, Napoli Ferreira CC, Casali Da Rocha JC, Simpson CC, Simpson AJ.

Ann Surg Oncol. 2002 Jul;9(6):555-61.

PMID:
12095971
3.

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

Hampel H, Stephens JA, Pukkala E, Sankila R, Aaltonen LA, Mecklin JP, de la Chapelle A.

Gastroenterology. 2005 Aug;129(2):415-21.

PMID:
16083698
4.

Association between family history and mismatch repair in colorectal cancer.

Coggins RP, Cawkwell L, Bell SM, Crockford GP, Quirke P, Finan PJ, Bishop DT.

Gut. 2005 May;54(5):636-42.

5.
6.

Frequency of hereditary non-polyposis colorectal cancer among Uruguayan patients with colorectal cancer.

Sarroca C, Valle AD, Fresco R, Renkonen E, Peltömaki P, Lynch H.

Clin Genet. 2005 Jul;68(1):80-7.

PMID:
15952990
7.
8.

p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population.

Jones JS, Chi X, Gu X, Lynch PM, Amos CI, Frazier ML.

Clin Cancer Res. 2004 Sep 1;10(17):5845-9.

9.
10.

Risk of colon cancer in hereditary non-polyposis colorectal cancer patients as predicted by fuzzy modeling: Influence of smoking.

Brand RM, Jones DD, Lynch HT, Brand RE, Watson P, Ashwathnayaran R, Roy HK.

World J Gastroenterol. 2006 Jul 28;12(28):4485-91.

11.

[Detection mutations in the DNA mismatch repair genes of hMLH1 and hMSH2 genes in Colombian families with suspicion of hereditary non-polyposis colorectal carcinoma (Lynch syndrome)].

Gómez A, Salguero G, García H, Aristizábal F, Gutiérrez O, Angel LA, Padrón J, Martínez C, Martínez H, Malaver O, Barvo R, Giraldo A.

Biomedica. 2005 Sep;25(3):315-24. Spanish.

PMID:
16276679
12.

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.

13.

[Comparison of clinical and genetic phenotypes between Chinese and Korean hereditary nonpolyposis colorectal cancer families].

Shen H, Yuan Y, Song YM, Huang YQ, Zheng S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Jun;25(3):326-30. Chinese.

PMID:
18543228
14.

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer.

Järvinen HJ, Aarnio M, Mustonen H, Aktan-Collan K, Aaltonen LA, Peltomäki P, De La Chapelle A, Mecklin JP.

Gastroenterology. 2000 May;118(5):829-34.

PMID:
10784581
15.

Hereditary nonpolyposis colorectal cancer (Lynch syndrome): criteria for identification and management.

Kouraklis G, Misiakos EP.

Dig Dis Sci. 2005 Feb;50(2):336-44. Review.

PMID:
15745097
16.

The hMSH2 and hMLH1 genes in hereditary nonpolyposis colorectal cancer.

Lynch PM.

Surg Oncol Clin N Am. 2009 Oct;18(4):611-24. doi: 10.1016/j.soc.2009.08.002. Review.

PMID:
19793569
17.

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

Vasen HF, Wijnen JT, Menko FH, Kleibeuker JH, Taal BG, Griffioen G, Nagengast FM, Meijers-Heijboer EH, Bertario L, Varesco L, Bisgaard ML, Mohr J, Fodde R, Khan PM.

Gastroenterology. 1996 Apr;110(4):1020-7. Erratum in: Gastroenterology 1996 Nov;111(5):1402.

PMID:
8612988
18.

The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population.

Christensen LL, Madsen BE, Wikman FP, Wiuf C, Koed K, Tjønneland A, Olsen A, Syvänen AC, Andersen CL, Orntoft TF.

BMC Med Genet. 2008 Jun 11;9:52. doi: 10.1186/1471-2350-9-52.

19.

Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.

Järvinen HJ, Renkonen-Sinisalo L, Aktán-Collán K, Peltomäki P, Aaltonen LA, Mecklin JP.

J Clin Oncol. 2009 Oct 1;27(28):4793-7. doi: 10.1200/JCO.2009.23.7784. Epub 2009 Aug 31.

20.

Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia.

Lee SC, Guo JY, Lim R, Soo R, Koay E, Salto-Tellez M, Leong A, Goh BC.

Clin Genet. 2005 Aug;68(2):137-45.

PMID:
15996210
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