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Items: 1 to 20 of 100

1.

Underdiagnosis of Lynch syndrome involves more than family history criteria.

Singh H, Schiesser R, Anand G, Richardson PA, El-Serag HB.

Clin Gastroenterol Hepatol. 2010 Jun;8(6):523-9. doi: 10.1016/j.cgh.2010.03.010. Epub 2010 Mar 18.

2.

Underutilization of Lynch syndrome screening in a multisite study of patients with colorectal cancer.

Cross DS, Rahm AK, Kauffman TL, Webster J, Le AQ, Spencer Feigelson H, Alexander G, Meier P, Onitilo AA, Pawloski PA, Williams AE, Honda S, Daida Y, McCarty CA, Goddard KA; CERGEN study team.

Genet Med. 2013 Dec;15(12):933-40. doi: 10.1038/gim.2013.43. Epub 2013 May 2.

3.

Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.

Maradiegue A, Jasperson K, Edwards QT, Lowstuter K, Weitzel J.

J Am Acad Nurse Pract. 2008 Feb;20(2):76-84. doi: 10.1111/j.1745-7599.2007.00282.x. Review.

PMID:
18271762
4.

Outcomes of screening endometrial cancer patients for Lynch syndrome by patient-administered checklist.

Daniels MS, Urbauer DL, Zangeneh A, Batte BA, Dempsey KM, Lu KH.

Gynecol Oncol. 2013 Dec;131(3):619-23. doi: 10.1016/j.ygyno.2013.10.011. Epub 2013 Oct 17.

5.

Recording of family history is associated with colorectal cancer stage.

Kessels K, de Groot NL, Fidder HH, Timmer R, Stolk MF, Offerhaus GJ, Siersema PD; Familial Colorectal Cancer Study Group Utrecht.

Eur J Gastroenterol Hepatol. 2013 Apr;25(4):482-7. doi: 10.1097/MEG.0b013e32835c45a3.

PMID:
23470269
6.

Identification of Lynch syndrome among patients with colorectal cancer.

Moreira L, Balaguer F, Lindor N, de la Chapelle A, Hampel H, Aaltonen LA, Hopper JL, Le Marchand L, Gallinger S, Newcomb PA, Haile R, Thibodeau SN, Gunawardena S, Jenkins MA, Buchanan DD, Potter JD, Baron JA, Ahnen DJ, Moreno V, Andreu M, Ponz de Leon M, Rustgi AK, Castells A; EPICOLON Consortium.

JAMA. 2012 Oct 17;308(15):1555-65. doi: 10.1001/jama.2012.13088.

7.

Increasing Lynch syndrome identification through establishment of a hereditary colorectal cancer registry.

Sturgeon D, McCutcheon T, Geiger TM, Muldoon RL, Herline AJ, Wise PE.

Dis Colon Rectum. 2013 Mar;56(3):308-14. doi: 10.1097/DCR.0b013e31827edfff.

PMID:
23392144
8.

Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data.

van Dijk DA, Oostindiër MJ, Kloosterman-Boele WM, Krijnen P, Vasen HF; Hereditary Tumor Study Group of the Comprehensive Cancer Centre West.

Fam Cancer. 2007;6(1):131-4.

9.

Performance characteristics of a brief Family History Questionnaire to screen for Lynch syndrome in women with newly diagnosed endometrial cancer.

Eiriksson L, Aronson M, Clarke B, Mojtahedi G, Massey C, Oza AM, Gallinger S, Pollett A, Mackay H, Bernardini MQ, Ferguson SE.

Gynecol Oncol. 2015 Feb;136(2):311-6. doi: 10.1016/j.ygyno.2014.12.023. Epub 2014 Dec 19.

PMID:
25529831
10.

Uptake of genetic testing by relatives of lynch syndrome probands: a systematic review.

Sharaf RN, Myer P, Stave CD, Diamond LC, Ladabaum U.

Clin Gastroenterol Hepatol. 2013 Sep;11(9):1093-100. doi: 10.1016/j.cgh.2013.04.044. Epub 2013 May 10. Review.

PMID:
23669308
11.

Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers.

Hunter JE, Zepp JM, Gilmore MJ, Davis JV, Esterberg EJ, Muessig KR, Peterson SK, Syngal S, Acheson LS, Wiesner GL, Reiss JA, Goddard KA.

Cancer. 2015 Sep 15;121(18):3281-9. doi: 10.1002/cncr.29470. Epub 2015 Jun 2.

12.

Improving identification of lynch syndrome patients: a comparison of research data with clinical records.

Tan YY, McGaughran J, Ferguson K, Walsh MD, Buchanan DD, Young JP, Webb PM, Obermair A, Spurdle AB; ANECS Group.

Int J Cancer. 2013 Jun 15;132(12):2876-83. doi: 10.1002/ijc.27978. Epub 2013 Jan 11.

13.

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.

14.

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.

Yurgelun MB, Allen B, Kaldate RR, Bowles KR, Judkins T, Kaushik P, Roa BB, Wenstrup RJ, Hartman AR, Syngal S.

Gastroenterology. 2015 Sep;149(3):604-13.e20. doi: 10.1053/j.gastro.2015.05.006. Epub 2015 May 14.

15.

Understanding Lynch syndrome: implications for nursing.

Bannon E, Coleman EA.

Clin J Oncol Nurs. 2007 Jun;11(3):423-7. Review.

PMID:
17623626
16.

Performance of Lynch syndrome predictive models in a multi-center US referral population.

Khan O, Blanco A, Conrad P, Gulden C, Moss TZ, Olopade OI, Kupfer SS, Terdiman J.

Am J Gastroenterol. 2011 Oct;106(10):1822-7; quiz 1828. doi: 10.1038/ajg.2011.200. Epub 2011 Jul 12.

17.

Lynch syndrome screening in newly diagnosed colorectal cancer in general pathology practice: from the revised Bethesda guidelines to a universal approach.

Morrison J, Bronner M, Leach BH, Downs-Kelly E, Goldblum JR, Liu X.

Scand J Gastroenterol. 2011 Nov;46(11):1340-8. doi: 10.3109/00365521.2011.610003. Epub 2011 Aug 31.

PMID:
21879804
18.

Evaluating Lynch syndrome in very early onset colorectal cancer probands without apparent polyposis.

Jasperson KW, Vu TM, Schwab AL, Neklason DW, Rodriguez-Bigas MA, Burt RW, Weitzel JN.

Fam Cancer. 2010 Jun;9(2):99-107. doi: 10.1007/s10689-009-9290-4. Erratum in: Fam Cancer. 2013 Sep;12(3):583.

19.

Clinical guidelines versus universal molecular testing: are we ready to choose an optimal strategy for Lynch syndrome identification?

Byfield SA, Syngal S.

Am J Gastroenterol. 2008 Nov;103(11):2837-40. doi: 10.1111/j.1572-0241.2008.02091.x.

20.

Awareness of heredity in colorectal cancer patients is insufficient among clinicians: a Norwegian population-based study.

Tranø G, Wasmuth HH, Sjursen W, Hofsli E, Vatten LJ.

Colorectal Dis. 2009 Jun;11(5):456-61. doi: 10.1111/j.1463-1318.2009.01830.x. Epub 2009 Mar 11.

PMID:
19508550

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