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Items: 1 to 20 of 113

1.

Unusual DNA mismatch repair-deficient tumors in Lynch syndrome: a report of new cases and review of the literature.

Karamurzin Y, Zeng Z, Stadler ZK, Zhang L, Ouansafi I, Al-Ahmadie HA, Sempoux C, Saltz LB, Soslow RA, O'Reilly EM, Paty PB, Coit DG, Shia J, Klimstra DS.

Hum Pathol. 2012 Oct;43(10):1677-87. doi: 10.1016/j.humpath.2011.12.012. Epub 2012 Apr 17. Review.

PMID:
22516243
2.

Synchronous breast cancers with different morphologic and molecular phenotypes occurring in Lynch syndrome: what does the heterogeneity imply?

D'Arcy C, Wen YH, Stadler ZK, Brogi E, Shia J.

Am J Surg Pathol. 2011 Nov;35(11):1743-8. doi: 10.1097/PAS.0b013e3182320cff. Erratum in: Am J Surg Pathol. 2012 Mar;36(3):477.

PMID:
21997695
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.

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
5.

Mismatch repair genes in Lynch syndrome: a review.

Silva FC, Valentin MD, Ferreira Fde O, Carraro DM, Rossi BM.

Sao Paulo Med J. 2009 Jan;127(1):46-51. Review.

6.

Lynch syndrome and related familial colorectal cancers.

Abdel-Rahman WM, Peltomäki P.

Crit Rev Oncog. 2008;14(1):1-22; discussion 23-31. Review.

PMID:
19105568
7.

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
8.

Microsatellite instability in saliva from patients with hereditary non-polyposis colon cancer and siblings carrying germline mismatch repair gene mutations.

Hu P, Lee CW, Xu JP, Simien C, Fan CL, Tam M, Ramagli L, Brown BW, Lynch P, Frazier ML, Siciliano MJ, Coolbaugh-Murphy M.

Ann Clin Lab Sci. 2011 Fall;41(4):321-30.

PMID:
22166501
9.

Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.

Ferreira AM, Westers H, Sousa S, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, Reuvekamp PT, Seruca R, Kleibeuker JH, Hollema H, Sijmons RH, Hofstra RM.

J Pathol. 2009 Sep;219(1):96-102. doi: 10.1002/path.2573.

PMID:
19521971
10.

A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome.

Perera S, Ramyar L, Mitri A, Pollett A, Gallinger S, Speevak MD, Aronson M, Bapat B.

J Hum Genet. 2010 Jan;55(1):37-41. doi: 10.1038/jhg.2009.119. Epub 2009 Nov 13.

PMID:
19911012
11.

Detecting Lynch syndrome by pathologists.

van Krieken JH, Kets CM, Ligtenberg MJ, Hoogerbrugge N.

Verh Dtsch Ges Pathol. 2007;91:104-11.

PMID:
18314603
12.

Lynch or not Lynch? Is that always a question?

Colas C, Coulet F, Svrcek M, Collura A, Fléjou JF, Duval A, Hamelin R.

Adv Cancer Res. 2012;113:121-66. doi: 10.1016/B978-0-12-394280-7.00004-X. Review.

PMID:
22429854
13.

Medullary carcinoma of the pancreas in a man with hereditary nonpolyposis colorectal cancer due to a mutation of the MSH2 mismatch repair gene.

Banville N, Geraghty R, Fox E, Leahy DT, Green A, Keegan D, Geoghegan J, O'Donoghue D, Hyland J, Sheahan K.

Hum Pathol. 2006 Nov;37(11):1498-502. Epub 2006 Sep 25.

PMID:
16996571
14.

Intraductal papillary mucinous neoplasm of the pancreas with loss of mismatch repair in a patient with Lynch syndrome.

Sparr JA, Bandipalliam P, Redston MS, Syngal S.

Am J Surg Pathol. 2009 Feb;33(2):309-12. doi: 10.1097/PAS.0b013e3181882c3d.

15.

The frequency of Muir-Torre syndrome among Lynch syndrome families.

South CD, Hampel H, Comeras I, Westman JA, Frankel WL, de la Chapelle A.

J Natl Cancer Inst. 2008 Feb 20;100(4):277-81. doi: 10.1093/jnci/djm291. Epub 2008 Feb 12.

PMID:
18270343
16.

Pathogenicity of A600V variant in exon 12 of the MSH2 gene detected in a Japanese kindred with Lynch syndrome.

Miyakura Y, Sugano K, Nomizu T, Lefor A, Yasuda Y.

Jpn J Clin Oncol. 2012 Jan;42(1):78-82. doi: 10.1093/jjco/hyr162. Epub 2011 Nov 14.

PMID:
22086974
17.

Deficient DNA mismatch repair is common in Lynch syndrome-associated colorectal adenomas.

Pino MS, Mino-Kenudson M, Wildemore BM, Ganguly A, Batten J, Sperduti I, Iafrate AJ, Chung DC.

J Mol Diagn. 2009 May;11(3):238-47. doi: 10.2353/jmoldx.2009.080142. Epub 2009 Mar 26.

18.

[Recognition of congenital endometrial carcinoma: the importance of family history and investigation of microsatellite instability in the tumour].

Hoogerbrugge N, Overbeek LI, de Hullu J, Kets CM, Hebeda KM, Ligtenberg MJ.

Ned Tijdschr Geneeskd. 2007 Jun 30;151(26):1441-4. Dutch.

PMID:
17633970
19.

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.

20.

Challenges in the diagnosis and management of Lynch Syndrome in an Indigenous family living in a remote West Australian community.

Schofield L, Goldblatt J, Iacopetta B.

Rural Remote Health. 2011;11(4):1836. Epub 2011 Dec 22.

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