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Items: 1 to 20 of 79

1.

Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.

Stulp RP, Herkert JC, Karrenbeld A, Mol B, Vos YJ, Sijmons RH.

Hered Cancer Clin Pract. 2008 Feb 15;6(1):15-21. doi: 10.1186/1897-4287-6-1-15.

2.

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
3.

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
4.

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
5.

Defective mismatch-repair in patients with multiple primary tumours including colorectal cancer.

Ericson K, Halvarsson B, Nagel J, Rambech E, Planck M, Piotrowska Z, Olsson H, Nilbert M.

Eur J Cancer. 2003 Jan;39(2):240-8.

PMID:
12509957
6.

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.

7.

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.

8.

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
9.

Prevalence of the mismatch-repair-deficient phenotype in colonic adenomas arising in HNPCC patients: results of a 5-year follow-up study.

German HNPCC Consortium, Müller A, Beckmann C, Westphal G, Bocker Edmonston T, Friedrichs N, Dietmaier W, Brasch FE, Kloor M, Poremba C, Keller G, Aust DE, Fass J, Büttner R, Becker H, Rüschoff J.

Int J Colorectal Dis. 2006 Oct;21(7):632-41. Epub 2006 Mar 2.

PMID:
16511680
11.

Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC).

Glasl S, Papatheodorou L, Baretton G, Jung C, Gross M.

Hum Mutat. 2000 Jul;16(1):91-2.

PMID:
10874318
12.

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
13.

Efficient detection of hereditary nonpolyposis colorectal cancer gene carriers by screening for tumor microsatellite instability before germline genetic testing.

Terdiman JP, Gum JR Jr, Conrad PG, Miller GA, Weinberg V, Crawley SC, Levin TR, Reeves C, Schmitt A, Hepburn M, Sleisenger MH, Kim YS.

Gastroenterology. 2001 Jan;120(1):21-30.

PMID:
11208710
14.

[Lynch syndrome I: a case report].

Zivković V, Katić V, Gligorijević J, Andelković Z, Petrović A, Krstić M.

Med Pregl. 2008 Jan-Feb;61(1-2):79-82. Serbian.

PMID:
18798480
15.

[Mismatch repair (MMR) efficiency and MSH2 gene mutation in human colorectal carcinoma cell line COLO320HSR].

Tronov VA, Kramarenko II, Maĭorova EN, Zakharov SF.

Genetika. 2007 Apr;43(4):537-44. Russian.

PMID:
17555131
16.

[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
17.

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
18.

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
19.

A novel MSH2 germline mutation in homozygous state in two brothers with colorectal cancers diagnosed at the age of 11 and 12 years.

Müller A, Schackert HK, Lange B, Rüschoff J, Füzesi L, Willert J, Burfeind P, Shah P, Becker H, Epplen JT, Stemmler S.

Am J Med Genet A. 2006 Feb 1;140(3):195-9.

PMID:
16372347
20.

A database to support the interpretation of human mismatch repair gene variants.

Ou J, Niessen RC, Vonk J, Westers H, Hofstra RM, Sijmons RH.

Hum Mutat. 2008 Nov;29(11):1337-41. doi: 10.1002/humu.20907.

PMID:
18951442

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