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Toward a consensus in molecular diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome).
Lynch HT, Lynch JF, Lynch PM. Lynch HT, et al. Among authors: lynch jf, lynch pm. J Natl Cancer Inst. 2007 Feb 21;99(4):261-3. doi: 10.1093/jnci/djk077. J Natl Cancer Inst. 2007. PMID: 17312298 No abstract available.
Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications.
Lynch HT, Lynch PM, Lanspa SJ, Snyder CL, Lynch JF, Boland CR. Lynch HT, et al. Among authors: lynch pm, lynch jf. Clin Genet. 2009 Jul;76(1):1-18. doi: 10.1111/j.1399-0004.2009.01230.x. Clin Genet. 2009. PMID: 19659756 Free PMC article. Review.
More than one million patients will manifest colorectal cancer (CRC) this year of which, conservatively, approximately 3% (approximately 30,700 cases) will have Lynch syndrome (LS), the most common hereditary CRC predisposing syndrome. ...
More than one million patients will manifest colorectal cancer (CRC) this year of which, conservatively, approximately 3% (approximately 30, …
Adenocarcinoma of the small bowel in lynch syndrome II.
Lynch HT, Smyrk TC, Lynch PM, Lanspa SJ, Boman BM, Ens J, Lynch JF, Strayhorn P, Carmody T, Cristofaro G. Lynch HT, et al. Among authors: lynch pm, lynch jf. Cancer. 1989 Nov 15;64(10):2178-83. doi: 10.1002/1097-0142(19891115)64:10<2178::aid-cncr2820641033>3.0.co;2-0. Cancer. 1989. PMID: 2804907
We report adenocarcinoma of the small bowel in nine patients from eight Lynch syndrome II extended pedigrees. Each affected patient was in the direct genetic lineage or manifested multiple primary cancers (stomach, colon, endometrium, and ovary) consonant with the tumor sp …
We report adenocarcinoma of the small bowel in nine patients from eight Lynch syndrome II extended pedigrees. Each affected patient w …
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.
Vasen HF, Watson P, Mecklin JP, Lynch HT. Vasen HF, et al. Among authors: lynch ht. Gastroenterology. 1999 Jun;116(6):1453-6. doi: 10.1016/s0016-5085(99)70510-x. Gastroenterology. 1999. PMID: 10348829 No abstract available.
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients.
Aaltonen LA, Peltomäki P, Mecklin JP, Järvinen H, Jass JR, Green JS, Lynch HT, Watson P, Tallqvist G, Juhola M, et al. Aaltonen LA, et al. Among authors: lynch ht. Cancer Res. 1994 Apr 1;54(7):1645-8. Cancer Res. 1994. PMID: 8137274
The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancer.
Vasen HF, Watson P, Mecklin JP, Jass JR, Green JS, Nomizu T, Müller H, Lynch HT. Vasen HF, et al. Among authors: lynch ht. Anticancer Res. 1994 Jul-Aug;14(4B):1675-8. Anticancer Res. 1994. PMID: 7979205
E2F-4 mutation in hereditary non-polyposis colorectal cancer.
Moriyama H, Sasamoto H, Kambara T, Matsubara N, Ikeda M, Baba S, Meltzer SJ, Lynch HT, Shimizu K, Tanaka N. Moriyama H, et al. Among authors: lynch ht. J Exp Clin Cancer Res. 2002 Jun;21(2):185-9. J Exp Clin Cancer Res. 2002. PMID: 12148576
Hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay.
Sarroca C, Alfano N, Bendin GT, Della Valle A, Dominguez A, Quadrelli R, Vaglio A, Mechoso B, Tinley ST, Harty AE, Lynch JF, Franklin BA, Kristo P, Smyrk TC, Peltomäki P, Lynch HT. Sarroca C, et al. Among authors: lynch jf, lynch ht. Dis Colon Rectum. 2000 Mar;43(3):353-60; discussion 360-2. doi: 10.1007/BF02258301. Dis Colon Rectum. 2000. PMID: 10733117
The Muir-Torre syndrome in kindreds with hereditary nonpolyposis colorectal cancer (Lynch syndrome): A classic obligation in preventive medicine.
Lynch HT, Fusaro RM. Lynch HT, et al. J Am Acad Dermatol. 1999 Nov;41(5 Pt 1):797-9. doi: 10.1016/s0190-9622(99)70017-4. J Am Acad Dermatol. 1999. PMID: 10534651 No abstract available.
Identifying hereditary nonpolyposis colorectal cancer.
Lynch HT, Smyrk TC. Lynch HT, et al. N Engl J Med. 1998 May 21;338(21):1537-8. doi: 10.1056/NEJM199805213382109. N Engl J Med. 1998. PMID: 9593794 No abstract available.
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