Format
Sort by
Items per page

Send to

Choose Destination

Best matches for hereditary colorectal cancer:

Hereditary Colorectal Cancer Syndromes. Wells K et al. Surg Clin North Am. (2017)

Population Screening for Hereditary Colorectal Cancer. Hampel H et al. Surg Oncol Clin N Am. (2018)

The Growing Challenge of Young Adults With Colorectal Cancer. Weinberg BA et al. Oncology (Williston Park). (2017)

Search results

Items: 1 to 20 of 7275

1.

Refining Risk Factors for Gastric Cancer in Patients With Lynch Syndrome to Optimize Surveillance Esophagogastroduodenoscopy.

Mankaney G, Macaron C, Burke CA.

Clin Gastroenterol Hepatol. 2019 Oct 10. pii: S1542-3565(19)31101-2. doi: 10.1016/j.cgh.2019.10.003. [Epub ahead of print] No abstract available.

PMID:
31606458
2.

The missing heritability of familial colorectal cancer.

Schubert SA, Morreau H, de Miranda NFCC, van Wezel T.

Mutagenesis. 2019 Oct 12. pii: gez027. doi: 10.1093/mutage/gez027. [Epub ahead of print]

PMID:
31605533
3.

Prophylactic Surgery and Extended Oncologic Radicality in Gastric and Colorectal Hereditary Cancer Syndromes.

Vogelsang HE.

Visc Med. 2019 Aug;35(4):231-239. doi: 10.1159/000501919. Epub 2019 Jul 16. Review.

PMID:
31602384
4.

Genetic Screening and Personalized Prevention in Colorectal Cancer.

Steinke-Lange V, Holinski-Feder E.

Visc Med. 2019 Aug;35(4):226-230. doi: 10.1159/000501941. Epub 2019 Jul 17. Review.

PMID:
31602383
5.

Endoscopic management of Lynch syndrome and of familial risk of colorectal cancer: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.

van Leerdam ME, Roos VH, van Hooft JE, Balaguer F, Dekker E, Kaminski MF, Latchford A, Neumann H, Ricciardiello L, Rupińska M, Saurin JC, Tanis PJ, Wagner A, Jover R, Pellisé M.

Endoscopy. 2019 Oct 9. doi: 10.1055/a-1016-4977. [Epub ahead of print]

6.

Spindle Cell Proliferations of the Sigmoid Colon, Rectum and Anus: A Review with Emphasis on Perineurioma.

Grech P, Schofield JB.

Histopathology. 2019 Oct 6. doi: 10.1111/his.14011. [Epub ahead of print] Review.

PMID:
31587346
7.

Pure Discrete Punctate Nuclear Staining Pattern for MLH1 Protein Does Not Represent Intact Nuclear Expression.

Zhang Q, Young GQ, Yang Z.

Int J Surg Pathol. 2019 Sep 29:1066896919878830. doi: 10.1177/1066896919878830. [Epub ahead of print]

PMID:
31566049
8.

Carcinoma of the colon in a 40 year old female: a case report.

Walubembe J, Aremo ME, Tumwine C, Nabaale F, Twinomasiko A, Tukesiga I, Ssenyomo P, Mugaiga A, Semakula JR, Olwedo DA, Kitara DL.

Pan Afr Med J. 2019 Jul 3;33:161. doi: 10.11604/pamj.2019.33.161.12383. eCollection 2019.

9.

[Identification and management of patients with Lynch syndrome].

Coffin E, Dhooge M, Abou Ali E, Dermine S, Lavole J, Palmieri LJ, Chaussade S, Coriat R.

Presse Med. 2019 Sep 24. pii: S0755-4982(19)30298-2. doi: 10.1016/j.lpm.2019.07.011. [Epub ahead of print] French.

PMID:
31561847
10.

Genetic Counseling and Surveillance Focused on Lynch Syndrome.

Kim JY, Byeon JS.

J Anus Rectum Colon. 2019 Apr 25;3(2):60-68. doi: 10.23922/jarc.2019-002. eCollection 2019. Review.

11.

For women Lynch syndrome is about more than colon cancer.

Parker WM, Hennig K, Burton-Chase AM.

Cancer Prev Res (Phila). 2019 Sep 25. pii: canprevres.0069.2019. doi: 10.1158/1940-6207.CAPR-19-0069. [Epub ahead of print]

PMID:
31554630
12.

Microsatellite Instability in Endometrial Carcinoma by Immunohistochemistry, Association with Clinical and Histopathologic Parameters.

Hashmi AA, Mudassir G, Hashmi RN, Irfan M, Asif H, Khan EY, Abu Bakar SM, Faridi N.

Asian Pac J Cancer Prev. 2019 Sep 1;20(9):2601-2606. doi: 10.31557/APJCP.2019.20.9.2601.

13.

Tumour budding predicts increased recurrence after curative resection for T2N0 colorectal cancer

Garfinkle R, Lee L, Boutros M, Cardin MJ, Spatz A, Morin N.

Can J Surg. 2019 Oct 1;62(5):334-339.

14.

Publisher Correction: Shared heritability and functional enrichment across six solid cancers.

Jiang X, Finucane HK, Schumacher FR, Schmit SL, Tyrer JP, Han Y, Michailidou K, Lesseur C, Kuchenbaecker KB, Dennis J, Conti DV, Casey G, Gaudet MM, Huyghe JR, Albanes D, Aldrich MC, Andrew AS, Andrulis IL, Anton-Culver H, Antoniou AC, Antonenkova NN, Arnold SM, Aronson KJ, Arun BK, Bandera EV, Barkardottir RB, Barnes DR, Batra J, Beckmann MW, Benitez J, Benlloch S, Berchuck A, Berndt SI, Bickeböller H, Bien SA, Blomqvist C, Boccia S, Bogdanova NV, Bojesen SE, Bolla MK, Brauch H, Brenner H, Brenton JD, Brook MN, Brunet J, Brunnström H, Buchanan DD, Burwinkel B, Butzow R, Cadoni G, Caldés T, Caligo MA, Campbell I, Campbell PT, Cancel-Tassin G, Cannon-Albright L, Campa D, Caporaso N, Carvalho AL, Chan AT, Chang-Claude J, Chanock SJ, Chen C, Christiani DC, Claes KBM, Claessens F, Clements J, Collée JM, Correa MC, Couch FJ, Cox A, Cunningham JM, Cybulski C, Czene K, Daly MB, deFazio A, Devilee P, Diez O, Gago-Dominguez M, Donovan JL, Dörk T, Duell EJ, Dunning AM, Dwek M, Eccles DM, Edlund CK, Edwards DRV, Ellberg C, Evans DG, Fasching PA, Ferris RL, Liloglou T, Figueiredo JC, Fletcher O, Fortner RT, Fostira F, Franceschi S, Friedman E, Gallinger SJ, Ganz PA, Garber J, García-Sáenz JA, Gayther SA, Giles GG, Godwin AK, Goldberg MS, Goldgar DE, Goode EL, Goodman MT, Goodman G, Grankvist K, Greene MH, Gronberg H, Gronwald J, Guénel P, Håkansson N, Hall P, Hamann U, Hamdy FC, Hamilton RJ, Hampe J, Haugen A, Heitz F, Herrero R, Hillemanns P, Hoffmeister M, Høgdall E, Hong YC, Hopper JL, Houlston R, Hulick PJ, Hunter DJ, Huntsman DG, Idos G, Imyanitov EN, Ingles SA, Isaacs C, Jakubowska A, James P, Jenkins MA, Johansson M, Johansson M, John EM, Joshi AD, Kaneva R, Karlan BY, Kelemen LE, Kühl T, Khaw KT, Khusnutdinova E, Kibel AS, Kiemeney LA, Kim J, Kjaer SK, Knight JA, Kogevinas M, Kote-Jarai Z, Koutros S, Kristensen VN, Kupryjanczyk J, Lacko M, Lam S, Lambrechts D, Landi MT, Lazarus P, Le ND, Lee E, Lejbkowicz F, Lenz HJ, Leslie G, Lessel D, Lester J, Levine DA, Li L, Li CI, Lindblom A, Lindor NM, Liu G, Loupakis F, Lubiński J, Maehle L, Maier C, Mannermaa A, Marchand LL, Margolin S, May T, McGuffog L, Meindl A, Middha P, Miller A, Milne RL, MacInnis RJ, Modugno F, Montagna M, Moreno V, Moysich KB, Mucci L, Muir K, Mulligan AM, Nathanson KL, Neal DE, Ness AR, Neuhausen SL, Nevanlinna H, Newcomb PA, Newcomb LF, Nielsen FC, Nikitina-Zake L, Nordestgaard BG, Nussbaum RL, Offit K, Olah E, Olama AAA, Olopade OI, Olshan AF, Olsson H, Osorio A, Pandha H, Park JY, Pashayan N, Parsons MT, Pejovic T, Penney KL, Peters WHM, Phelan CM, Phipps AI, Plaseska-Karanfilska D, Pring M, Prokofyeva D, Radice P, Stefansson K, Ramus SJ, Raskin L, Rennert G, Rennert HS, van Rensburg EJ, Riggan MJ, Risch HA, Risch A, Roobol MJ, Rosenstein BS, Rossing MA, De Ruyck K, Saloustros E, Sandler DP, Sawyer EJ, Schabath MB, Schleutker J, Schmidt MK, Setiawan VW, Shen H, Siegel EM, Sieh W, Singer CF, Slattery ML, Sorensen KD, Southey MC, Spurdle AB, Stanford JL, Stevens VL, Stintzing S, Stone J, Sundfeldt K, Sutphen R, Swerdlow AJ, Tajara EH, Tangen CM, Tardon A, Taylor JA, Teare MD, Teixeira MR, Terry MB, Terry KL, Thibodeau SN, Thomassen M, Bjørge L, Tischkowitz M, Toland AE, Torres D, Townsend PA, Travis RC, Tung N, Tworoger SS, Ulrich CM, Usmani N, Vachon CM, Van Nieuwenhuysen E, Vega A, Aguado-Barrera ME, Wang Q, Webb PM, Weinberg CR, Weinstein S, Weissler MC, Weitzel JN, West CML, White E, Whittemore AS, Wichmann HE, Wiklund F, Winqvist R, Wolk A, Woll P, Woods M, Wu AH, Wu X, Yannoukakos D, Zheng W, Zienolddiny S, Ziogas A, Zorn KK, Lane JM, Saxena R, Thomas D, Hung RJ, Diergaarde B, McKay J, Peters U, Hsu L, García-Closas M, Eeles RA, Chenevix-Trench G, Brennan PJ, Haiman CA, Simard J, Easton DF, Gruber SB, Pharoah PDP, Price AL, Pasaniuc B, Amos CI, Kraft P, Lindström S.

Nat Commun. 2019 Sep 23;10(1):4386. doi: 10.1038/s41467-019-12095-8.

15.

STELO: a new tool for family physicians for the correct identification of inherited cancer syndromes.

Mariani C, Carnevali I, Lapi F, Paganini E, Civitelli C, Muzzolon J, Franzetti A, Guerroni A, Tibiletti MG.

Fam Pract. 2019 Sep 19. pii: cmz045. doi: 10.1093/fampra/cmz045. [Epub ahead of print]

PMID:
31536618
16.

The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression.

Thomas R, Trapani D, Goodyer-Sait L, Tomkova M, Fernandez-Rozadilla C, Sahnane N, Woolley C, Davis H, Chegwidden L, Kriaucionis S, Maughan T, Leedham S, Palles C, Furlan D, Tomlinson I, Lewis A.

Sci Rep. 2019 Sep 17;9(1):13463. doi: 10.1038/s41598-019-49952-x.

17.

Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy.

Terlouw D, Suerink M, Singh SS, Gille HJJP, Hes FJ, Langers AMJ, Morreau H, Vasen HFA, Vos YJ, van Wezel T, Tops CM, Ten Broeke SW, Nielsen M.

Eur J Hum Genet. 2019 Sep 16. doi: 10.1038/s41431-019-0509-z. [Epub ahead of print]

PMID:
31527860
18.

Chromoendoscopy or white light endoscopy for neoplasia detection in Lynch syndrome, a meta-analysis.

Har-Noy O, Yung DE, Koulaouzidis A, Eliakim R, Kopylov U, Avidan B, Katz LH.

Dig Liver Dis. 2019 Sep 13. pii: S1590-8658(19)30720-0. doi: 10.1016/j.dld.2019.07.018. [Epub ahead of print] Review.

PMID:
31526715
19.

Lethal privacy: Quantifying life years lost if the right to informational self-determination guides genetic screening for Lynch syndrome.

Gansen F, Severin F, Schleidgen S, Marckmann G, Rogowski W.

Health Policy. 2019 Oct;123(10):1004-1010. doi: 10.1016/j.healthpol.2019.08.015. Epub 2019 Aug 27.

PMID:
31492458
20.

The spectrum of Lynch syndrome-associated germ-line mutations in Russia.

Yanus GA, Akhapkina TA, Iyevleva AG, Kornilov AV, Suspitsin EN, Kuligina ES, Ivantsov AO, Aleksakhina SN, Sokolova TN, Sokolenko AP, Togo AV, Imyanitov EN.

Eur J Med Genet. 2019 Sep 3:103753. doi: 10.1016/j.ejmg.2019.103753. [Epub ahead of print]

PMID:
31491536

Supplemental Content

Loading ...
Support Center