AGO Austria recommendation on screening and diagnosis of Lynch syndrome (LS)-Reference-Cited by-同舟云学术

AGO Austria recommendation on screening and diagnosis of Lynch syndrome (LS)

Published:2017-05-16 Issue:1 Volume:296 Page:123-127
ISSN:0932-0067
Container-title:Archives of Gynecology and Obstetrics
language:en
Short-container-title:Arch Gynecol Obstet

Author:

Zeimet Alain G.,Mori Harald,Petru Edgar,Polterauer Stephan,Reinthaller Alexander,Schauer Christian,Scholl-Firon Tonja,Singer Christian,Wimmer Katharina,Zschocke Johannes,Marth Christian

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynecology,General Medicine

Link

http://link.springer.com/article/10.1007/s00404-017-4392-y/fulltext.html

Reference17 articles.

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2. Ma J, Ledbetter N, Glenn L (2013) Testing women with endometrial cancer for lynch syndrome: should we test all? J Adv Pract Oncol 4:322–330

3. Lu KH, Wood ME, Daniels M, Burke C, Ford J, Kauff ND, Kohlmann W, Lindor NM, Mulvey TM, Robinson L, Rubinstein WS, Stoffel EM, Snyder C, Syngal S, Merrill JK, Wollins DS, Hughes KS, American Society of Clinical Oncology (2014) American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. J Clin Oncol 32:833–840

4. Buchanan DD, Tan YY, Walsh MD, Clendenning M, Metcalf AM, Ferguson K, Arnold ST, Thompson BA, Lose FA, Parsons MT, Walters RJ, Pearson SA, Cummings M, Oehler MK, Blomfield PB, Quinn MA, Kirk JA, Stewart CJ, Obermair A, Young JP, Webb PM, Spurdle AB (2014) Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing. J Clin Oncol 32:90–100

5. Hendriks YM, Wagner A, Morreau H, Menko F, Stormorken A, Quehenberger F, Sandkuijl L, Møller P, Genuardi M, Van Houwelingen H, Tops C, Van Puijenbroek M, Verkuijlen P, Kenter G, Van Mil A, Meijers-Heijboer H, Tan GB, Breuning MH, Fodde R, Wijnen JT, Bröcker-Vriends AH, Vasen H (2004) Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance. Gastroenterology 127:17–25

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