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Items: 1 to 20 of 201

1.

The genetics of HNPCC: application to diagnosis and screening.

Abdel-Rahman WM, Mecklin JP, Peltomäki P.

Crit Rev Oncol Hematol. 2006 Jun;58(3):208-20. Epub 2006 Jan 23. Review.

PMID:
16434208
2.

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
4.

The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications.

Chung DC, Rustgi AK.

Ann Intern Med. 2003 Apr 1;138(7):560-70. Review.

PMID:
12667026
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
6.

Women with synchronous primary cancers of the endometrium and ovary: do they have Lynch syndrome?

Soliman PT, Broaddus RR, Schmeler KM, Daniels MS, Gonzalez D, Slomovitz BM, Gershenson DM, Lu KH.

J Clin Oncol. 2005 Dec 20;23(36):9344-50.

PMID:
16361634
7.

Lynch Syndrome/Hereditary Non-polyposis Colorectal Cancer (HNPCC).

Stoffel EM.

Minerva Gastroenterol Dietol. 2010 Mar;56(1):45-53.

PMID:
20190724
8.

Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening.

Julié C, Trésallet C, Brouquet A, Vallot C, Zimmermann U, Mitry E, Radvanyi F, Rouleau E, Lidereau R, Coulet F, Olschwang S, Frébourg T, Rougier P, Nordlinger B, Laurent-Puig P, Penna C, Boileau C, Franc B, Muti C, Hofmann-Radvanyi H.

Am J Gastroenterol. 2008 Nov;103(11):2825-35; quiz 2836. doi: 10.1111/j.1572-0241.2008.02084.x. Epub 2008 Aug 27.

PMID:
18759827
9.

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
10.

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.

11.

[Essential to discover hereditary colorectal and endometrial cancer. Mutations in "HNPCC individuals" can cause several different tumors].

Nilbert M, Grönberg H, Lindblom A.

Lakartidningen. 2002 Aug 22;99(34):3296-300. Review. Swedish.

PMID:
12362848
12.

Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.

Cederquist K, Emanuelsson M, Wiklund F, Golovleva I, Palmqvist R, Grönberg H.

Clin Genet. 2005 Dec;68(6):533-41.

PMID:
16283884
13.

Genetic susceptibility to non-polyposis colorectal cancer.

Lynch HT, de la Chapelle A.

J Med Genet. 1999 Nov;36(11):801-18. Review.

14.

[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
15.

The genetics of hereditary non-polyposis colorectal cancer.

Gruber SB, Kohlmann W.

J Natl Compr Canc Netw. 2003 Jan;1(1):137-44. Review.

PMID:
19764157
16.

[Hereditary carcinoma: pathogenesis and diagnosis].

Jungck M.

Zentralbl Chir. 2000;125 Suppl 1:8-11. German.

PMID:
10929639
17.

Tumour spectrum of non-polyposis colorectal cancer (Lynch syndrome) on the island of Tenerife and influence of insularity on the clinical manifestations.

Medina-Arana V, Barrios Y, Fernández-Peralta A, Jiménez A, Salido E, González F, González-Aguilera JJ.

Eur J Cancer Prev. 2004 Feb;13(1):27-32.

PMID:
15075785
18.

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
19.

Identification and classification of hereditary nonpolyposis colorectal cancer (Lynch syndrome): adapting old concepts to recent advancements. Report from the Italian Association for the study of Hereditary Colorectal Tumors Consensus Group.

Ponz de Leon M, Bertario L, Genuardi M, Lanza G, Oliani C, Ranzani GN, Rossi GB, Varesco L, Venesio T, Viel A.

Dis Colon Rectum. 2007 Dec;50(12):2126-34. Epub 2007 Sep 27. Review.

PMID:
17899274
20.

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

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