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Items: 1 to 20 of 114

1.

Familial colorectal cancer type X: polyp burden and cancer risk stratification via a family history score.

Koh PK, Kalady M, Skacel M, Fay S, McGannon E, Shenal J, Arroyo L, Toderick K, Church J.

ANZ J Surg. 2011 Jul-Aug;81(7-8):537-42.

PMID:
22295380
2.

Is the phenotype mixed or mistaken? Hereditary nonpolyposis colorectal cancer and hyperplastic polyposis syndrome.

Jarrar AM, Church JM, Fay S, Kalady MF.

Dis Colon Rectum. 2009 Dec;52(12):1949-55. doi: 10.1007/DCR.0b013e3181b5450c.

PMID:
19934914
3.

Patient and tumor characteristics may raise clinicians' awareness of familial colorectal cancer: a Norwegian population-based study.

Tranø G, Wasmuth H, Sjursen W, Vatten L.

Scand J Gastroenterol. 2011 Oct;46(10):1236-42. doi: 10.3109/00365521.2011.594086. Epub 2011 Jun 17.

PMID:
21679123
4.

Metachronous serrated neoplasia is uncommon after right colectomy in patients with methylator colon cancers with a high degree of microsatellite instability.

Messick CA, Kravochuck S, Church JM, Kalady MF.

Dis Colon Rectum. 2014 Jan;57(1):39-46. doi: 10.1097/01.dcr.0000437690.18709.76.

PMID:
24316944
5.
6.

Characterization of mutator phenotype in familial colorectal cancer patients not fulfilling amsterdam criteria.

Kim JC, Lee KH, Ka IH, Koo KH, Roh SA, Kim HC, Yu CS, Kim TW, Chang HM, Gong GY, Kim JS.

Clin Cancer Res. 2004 Sep 15;10(18 Pt 1):6159-68.

8.

Evaluation of Bethesda guidelines in relation to microsatellite instability.

Wüllenweber HP, Sutter C, Autschbach F, Willeke F, Kienle P, Benner A, Bähring J, Kadmon M, Herfarth C, von Knebel Doeberitz M, Gebert J.

Dis Colon Rectum. 2001 Sep;44(9):1281-9.

PMID:
11584201
9.

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
10.

Early-age-at-onset colorectal cancer and microsatellite instability as markers of hereditary nonpolyposis colorectal cancer.

Pucciarelli S, Agostini M, Viel A, Bertorelle R, Russo V, Toppan P, Lise M.

Dis Colon Rectum. 2003 Mar;46(3):305-12.

PMID:
12626904
11.

Phenotypic characteristics of hereditary non-polyposis colorectal cancer by the Amsterdam criteria: an Asian perspective.

Chew MH, Koh PK, Ng KH, Lim JF, Ho KS, Ooi BS, Tang CL, Eu KW.

ANZ J Surg. 2008 Jul;78(7):556-60. doi: 10.1111/j.1445-2197.2008.04570.x.

PMID:
18593409
12.

Identification of the methylator (serrated) colorectal cancer phenotype through precursor serrated polyps.

Messick CA, Church J, Casey G, Kalady MF.

Dis Colon Rectum. 2009 Sep;52(9):1535-41. doi: 10.1007/DCR.0b013e3181afbe05.

PMID:
19690479
13.

Hereditary colorectal cancer diagnostics: morphological features of familial colorectal cancer type X versus Lynch syndrome.

Klarskov L, Holck S, Bernstein I, Nilbert M.

J Clin Pathol. 2012 Apr;65(4):352-6. doi: 10.1136/jclinpath-2011-200535. Epub 2012 Jan 28.

PMID:
22287689
14.

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A.

N Engl J Med. 2005 May 5;352(18):1851-60.

15.

Prospective results of surveillance colonoscopy in dominant familial colorectal cancer with and without Lynch syndrome.

Dove-Edwin I, de Jong AE, Adams J, Mesher D, Lipton L, Sasieni P, Vasen HF, Thomas HJ.

Gastroenterology. 2006 Jun;130(7):1995-2000.

PMID:
16762622
16.
17.

Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants: report by the colorectal adenoma/carcinoma prevention programme 2.

Liljegren A, Barker G, Elliott F, Bertario L, Bisgaard ML, Eccles D, Evans G, Macrae F, Maher E, Lindblom A, Rotstein S, Nilsson B, Mecklin JP, Möslein G, Jass J, Fodde R, Mathers J, Burn J, Bishop DT.

J Clin Oncol. 2008 Jul 10;26(20):3434-9. doi: 10.1200/JCO.2007.13.2795.

18.

Patterns of surgery in patients belonging to amsterdam-positive families.

Van Dalen R, Church J, McGannon E, Fay S, Burke C, Clark B.

Dis Colon Rectum. 2003 May;46(5):617-20.

PMID:
12792437
19.

Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome.

van Lier MG, Leenen CH, Wagner A, Ramsoekh D, Dubbink HJ, van den Ouweland AM, Westenend PJ, de Graaf EJ, Wolters LM, Vrijland WW, Kuipers EJ, van Leerdam ME, Steyerberg EW, Dinjens WN; LIMO Study Group.

J Pathol. 2012 Apr;226(5):764-74. doi: 10.1002/path.3963. Epub 2012 Jan 17.

PMID:
22081473
20.

In Lynch syndrome adenomas, loss of mismatch repair proteins is related to an enhanced lymphocytic response.

Meijer TW, Hoogerbrugge N, Nagengast FM, Ligtenberg MJ, van Krieken JH.

Histopathology. 2009 Oct;55(4):414-22. doi: 10.1111/j.1365-2559.2009.03403.x.

PMID:
19817892
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