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Items: 1 to 20 of 44

1.

Selecting patients with young-onset colorectal cancer for mismatch repair gene analysis.

Walker M, O'Sullivan B, Perakath B, Taniere P, Cruger D, Morton D.

Br J Surg. 2007 Dec;94(12):1567-71.

PMID:
17665423
2.

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
3.

Selection of endometrial carcinomas for DNA mismatch repair protein immunohistochemistry using patient age and tumor morphology enhances detection of mismatch repair abnormalities.

Garg K, Leitao MM Jr, Kauff ND, Hansen J, Kosarin K, Shia J, Soslow RA.

Am J Surg Pathol. 2009 Jun;33(6):925-33. doi: 10.1097/PAS.0b013e318197a046.

PMID:
19238076
4.

Strategy in clinical practice for classification of unselected colorectal tumours based on mismatch repair deficiency.

Jensen LH, Lindebjerg J, Byriel L, Kolvraa S, Crüger DG.

Colorectal Dis. 2008 Jun;10(5):490-7. Epub 2007 Sep 13.

PMID:
17868408
5.
6.

[Study on the germline mutation of MSH6 gene in Chinese hereditary nonpolyposis colorectal cancer pedigrees using PCR based sequencing].

Yan SY, Zhou XY, Cai SJ, Yu BH, Zhang TM, Li XM, Lu YM, Zhou HH, Mo SJ, Du X, Shi DR.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Dec;24(6):640-5. Chinese.

PMID:
18067074
7.

Malignant melanoma in patients with hereditary nonpolyposis colorectal cancer.

Ponti G, Losi L, Pellacani G, Wannesson L, Cesinaro AM, Venesio T, Petti C, Seidenari S.

Br J Dermatol. 2008 Jul;159(1):162-8. doi: 10.1111/j.1365-2133.2008.08575.x. Epub 2008 Jul 1.

PMID:
18460031
8.

Report of a family segregating mutations in both the APC and MSH2 genes: juvenile onset of colorectal cancer in a double heterozygote.

Uhrhammer N, Bignon YJ.

Int J Colorectal Dis. 2008 Nov;23(11):1131-5. doi: 10.1007/s00384-008-0526-9. Epub 2008 Jul 16.

PMID:
18629513
9.

Genetic testing in gastroenterology: Lynch syndrome.

Grover S, Syngal S.

Best Pract Res Clin Gastroenterol. 2009;23(2):185-96. doi: 10.1016/j.bpg.2009.02.006. Review.

PMID:
19414145
10.

Prediction of Lynch syndrome in consecutive patients with colorectal cancer.

Green RC, Parfrey PS, Woods MO, Younghusband HB.

J Natl Cancer Inst. 2009 Mar 4;101(5):331-40. doi: 10.1093/jnci/djn499. Epub 2009 Feb 24.

PMID:
19244167
11.

Synchronous lung tumours in a patient with metachronous colorectal carcinoma and a germline MSH2 mutation.

Canney A, Sheahan K, Keegan D, Tolan M, Hyland J, Green A.

J Clin Pathol. 2009 May;62(5):471-3. doi: 10.1136/jcp.2008.063008.

PMID:
19398597
12.

Molecular analysis of colorectal cancer tumors from patients with mismatch repair proficient hereditary nonpolyposis colorectal cancer suggests novel carcinogenic pathways.

Sánchez-de-Abajo A, de la Hoya M, van Puijenbroek M, Tosar A, López-Asenjo JA, Díaz-Rubio E, Morreau H, Caldes T.

Clin Cancer Res. 2007 Oct 1;13(19):5729-35.

13.

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations.

Barrow E, Alduaij W, Robinson L, Shenton A, Clancy T, Lalloo F, Hill J, Evans DG.

Clin Genet. 2008 Sep;74(3):233-42. doi: 10.1111/j.1399-0004.2008.01035.x. Epub 2008 Jun 28.

PMID:
18554281
14.

Underutilization of microsatellite instability analysis in colorectal cancer patients at high risk for Lynch syndrome.

Van Lier MG, De Wilt JH, Wagemakers JJ, Dinjens WN, Damhuis RA, Wagner A, Kuipers EJ, Van Leerdam ME.

Scand J Gastroenterol. 2009;44(5):600-4. doi: 10.1080/00365520802706008.

PMID:
19153873
15.

High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers.

Grindedal EM, Blanco I, Stormorken A, Maehle L, Clark N, González S, Capella G, Vasen H, Burn J, Møller P.

Fam Cancer. 2009;8(2):145-51. doi: 10.1007/s10689-008-9219-3. Epub 2008 Oct 8.

PMID:
18841495
16.

The gastrointestinal phenotype of germline biallelic mismatch repair gene mutations.

Durno CA, Holter S, Sherman PM, Gallinger S.

Am J Gastroenterol. 2010 Nov;105(11):2449-56. doi: 10.1038/ajg.2010.215. Epub 2010 Jun 8.

PMID:
20531397
17.

Microsatellite instability and mismatch repair protein defects in ovarian epithelial neoplasms in patients 50 years of age and younger.

Jensen KC, Mariappan MR, Putcha GV, Husain A, Chun N, Ford JM, Schrijver I, Longacre TA.

Am J Surg Pathol. 2008 Jul;32(7):1029-37. doi: 10.1097/PAS.0b013e31816380c4.

PMID:
18469706
18.

Towards identification of hereditary DNA mismatch repair deficiency: sebaceous neoplasm warrants routine immunohistochemical screening regardless of patient's age or other clinical characteristics.

Orta L, Klimstra DS, Qin J, Mecca P, Tang LH, Busam KJ, Shia J.

Am J Surg Pathol. 2009 Jun;33(6):934-44. doi: 10.1097/PAS.0b013e318199edca.

PMID:
19342947
19.

[Multiple endocrine neoplasia type 1: recent developments and guidelines for DNA diagnosis and periodic clinical monitoring].

Dreijerink KM, Roijers JF, van der Luijt RB, Höppener JW, Lips CJ.

Ned Tijdschr Geneeskd. 2000 Dec 16;144(51):2445-9. Review. Dutch.

PMID:
11151652
20.

Review article: The Lynch syndrome (hereditary nonpolyposis colorectal cancer).

Vasen HF.

Aliment Pharmacol Ther. 2007 Dec;26 Suppl 2:113-26. doi: 10.1111/j.1365-2036.2007.03479.x. Review.

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