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Items: 1 to 20 of 101

1.

Communication, encouragement, and cancer screening in families with and without mutations for hereditary nonpolyposis colorectal cancer: a pilot study.

Ersig AL, Williams JK, Hadley DW, Koehly LM.

Genet Med. 2009 Oct;11(10):728-34. doi: 10.1097/GIM.0b013e3181b3f42d.

2.

Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.

Bonis PA, Trikalinos TA, Chung M, Chew P, Ip S, DeVine DA, Lau J.

Evid Rep Technol Assess (Full Rep). 2007 May;(150):1-180. Review.

3.
4.

Knowledge and Uptake of Genetic Counseling and Colonoscopic Screening Among Individuals at Increased Risk for Lynch Syndrome and their Endoscopists from the Family Health Promotion Project.

Patel SG, Ahnen DJ, Kinney AY, Horick N, Finkelstein DM, Hill DA, Lindor NM, MaCrae F, Lowery JT.

Am J Gastroenterol. 2016 Feb;111(2):285-93. doi: 10.1038/ajg.2015.397. Epub 2016 Feb 9.

5.

Explanations of risk in families without identified mutations for hereditary nonpolyposis colorectal cancer.

Ersig AL, Ayres L, Hadley DW, Koehly LM.

J Nurs Scholarsh. 2010 Jun;42(2):139-46. doi: 10.1111/j.1547-5069.2010.01342.x.

6.

Suspected hereditary nonpolyposis colorectal cancer: International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis.

Park JG, Vasen HF, Park KJ, Peltomaki P, Ponz de Leon M, Rodriguez-Bigas MA, Lubinski J, Beck NE, Bisgaard ML, Miyaki M, Wijnen JT, Baba S, Lynch HT.

Dis Colon Rectum. 1999 Jun;42(6):710-5; discussion 715-6.

PMID:
10378593
7.

How families communicate about HNPCC genetic testing: findings from a qualitative study.

Peterson SK, Watts BG, Koehly LM, Vernon SW, Baile WF, Kohlmann WK, Gritz ER.

Am J Med Genet C Semin Med Genet. 2003 May 15;119C(1):78-86.

PMID:
12704641
9.

Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families.

de Vos tot Nederveen Cappel WH, Nagengast FM, Griffioen G, Menko FH, Taal BG, Kleibeuker JH, Vasen HF.

Dis Colon Rectum. 2002 Dec;45(12):1588-94.

PMID:
12473880
10.

Mismatch repair gene mutation analysis and colonoscopy surveillance in Chinese Lynch syndrome families.

Fu L, Sheng JQ, Li XO, Jin P, Mu H, Han M, Huang JS, Sun ZQ, Li AQ, Wu ZT, Li SR.

Cell Oncol (Dordr). 2013 Jun;36(3):225-31. doi: 10.1007/s13402-013-0130-z. Epub 2013 May 3.

PMID:
23640085
11.

Screening adherence and cancer risk perceptions in colorectal cancer survivors with Lynch-like syndrome.

Katz LH, Burton-Chase AM, Advani S, Fellman B, Polivka KM, Yuan Y, Lynch PM, Peterson SK.

Clin Genet. 2016 Mar;89(3):392-8. doi: 10.1111/cge.12653. Epub 2015 Sep 14.

12.

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
13.

Surveillance colonoscopy in individuals at risk for hereditary nonpolyposis colorectal cancer: an evidence-based review.

Johnson PM, Gallinger S, McLeod RS.

Dis Colon Rectum. 2006 Jan;49(1):80-93; discussion 94-5.

PMID:
16284887
14.

Colon cancer screening practices after genetic counseling and testing for hereditary nonpolyposis colorectal cancer.

Hadley DW, Jenkins JF, Dimond E, de Carvalho M, Kirsch I, Palmer CG.

J Clin Oncol. 2004 Jan 1;22(1):39-44.

PMID:
14701766
15.

Family communication, genetic testing and colonoscopy screening in hereditary non-polyposis colon cancer: a qualitative study.

McCann S, MacAuley D, Barnett Y, Bunting B, Bradley A, Jeffers L, Morrison PJ.

Psychooncology. 2009 Nov;18(11):1208-15. doi: 10.1002/pon.1487.

PMID:
19177338
16.

Colon cancer screening practices following genetic testing for hereditary nonpolyposis colon cancer (HNPCC) mutations.

Halbert CH, Lynch H, Lynch J, Main D, Kucharski S, Rustgi AK, Lerman C.

Arch Intern Med. 2004 Sep 27;164(17):1881-7.

PMID:
15451763
17.

The importance of older family members in providing social resources and promoting cancer screening in families with a hereditary cancer syndrome.

Ashida S, Hadley DW, Goergen AF, Skapinsky KF, Devlin HC, Koehly LM.

Gerontologist. 2011 Dec;51(6):833-42. doi: 10.1093/geront/gnr049. Epub 2011 May 11.

18.

Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer.

Hadley DW, Jenkins J, Dimond E, Nakahara K, Grogan L, Liewehr DJ, Steinberg SM, Kirsch I.

Arch Intern Med. 2003 Mar 10;163(5):573-82.

PMID:
12622604
19.

Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing.

Aktan-Collan K, Haukkala A, Pylvänäinen K, Järvinen HJ, Aaltonen LA, Peltomäki P, Rantanen E, Kääriäinen H, Mecklin JP.

J Med Genet. 2007 Nov;44(11):732-8. Epub 2007 Jul 14.

20.

Changes in screening behaviors and attitudes toward screening from pre-test genetic counseling to post-disclosure in Lynch syndrome families.

Burton-Chase AM, Hovick SR, Peterson SK, Marani SK, Vernon SW, Amos CI, Frazier ML, Lynch PM, Gritz ER.

Clin Genet. 2013 Mar;83(3):215-20. doi: 10.1111/cge.12091.

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