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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 2
2004 3
2005 4
2006 2
2007 1
2009 2
2010 3
2011 2
2012 2
2013 1
2015 1
2016 1
2017 1
2018 4
2019 1
2020 1
2021 2
2022 3
2023 2
2024 1

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33 results

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Page 1
FDG-PET scanning in the diagnosis of gastrointestinal cancers.
van Kouwen MC, Oyen WJ, Nagengast FM, Jansen JB, Drenth JP. van Kouwen MC, et al. Scand J Gastroenterol Suppl. 2004;(241):85-92. doi: 10.1080/00855920410014614. Scand J Gastroenterol Suppl. 2004. PMID: 15696855 Review.
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy.
Suerink M, Ripperger T, Messiaen L, Menko FH, Bourdeaut F, Colas C, Jongmans M, Goldberg Y, Nielsen M, Muleris M, van Kouwen M, Slavc I, Kratz C, Vasen HF, Brugiѐres L, Legius E, Wimmer K. Suerink M, et al. Among authors: van kouwen m. J Med Genet. 2019 Feb;56(2):53-62. doi: 10.1136/jmedgenet-2018-105664. Epub 2018 Nov 10. J Med Genet. 2019. PMID: 30415209 Review.
Features of incident colorectal cancer in Lynch syndrome.
Argillander TE, Koornstra JJ, van Kouwen M, Langers AM, Nagengast FM, Vecht J, de Vos Tot Nederveen Cappel WH, Dekker E, van Duijvendijk P, Vasen HF. Argillander TE, et al. Among authors: van kouwen m. United European Gastroenterol J. 2018 Oct;6(8):1215-1222. doi: 10.1177/2050640618783554. Epub 2018 Jun 11. United European Gastroenterol J. 2018. PMID: 30288284 Free PMC article.
High yield of surveillance in patients diagnosed with constitutional mismatch repair deficiency.
Ghorbanoghli Z, van Kouwen M, Versluys B, Bonnet D, Devalck C, Tinat J, Januszkiewicz-Lewandowska D, Costas CC, Cottereau E, Hardwick JCH, Wimmer K, Brugieres L, Colas C, Vasen HFA. Ghorbanoghli Z, et al. Among authors: van kouwen m. J Med Genet. 2023 Jul;60(7):679-684. doi: 10.1136/jmg-2022-108829. Epub 2022 Nov 21. J Med Genet. 2023. PMID: 36411031
Does (supra)gastric belching trigger recurrent hiccups?
Hopman WP, van Kouwen MC, Smout AJ. Hopman WP, et al. Among authors: van kouwen mc. World J Gastroenterol. 2010 Apr 14;16(14):1795-9. doi: 10.3748/wjg.v16.i14.1795. World J Gastroenterol. 2010. PMID: 20380015 Free PMC article.
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome.
Engel C, Ahadova A, Seppälä TT, Aretz S, Bigirwamungu-Bargeman M, Bläker H, Bucksch K, Büttner R, de Vos Tot Nederveen Cappel WT, Endris V, Holinski-Feder E, Holzapfel S, Hüneburg R, Jacobs MAJM, Koornstra JJ, Langers AM, Lepistö A, Morak M, Möslein G, Peltomäki P, Pylvänäinen K, Rahner N, Renkonen-Sinisalo L, Schulmann K, Steinke-Lange V, Stenzinger A, Strassburg CP, van de Meeberg PC, van Kouwen M, van Leerdam M, Vangala DB, Vecht J, Verhulst ML, von Knebel Doeberitz M, Weitz J, Zachariae S, Loeffler M, Mecklin JP, Kloor M, Vasen HF; German HNPCC Consortium, the Dutch Lynch Syndrome Collaborative Group; Finnish Lynch Syndrome Registry. Engel C, et al. Among authors: van kouwen m. Gastroenterology. 2020 Apr;158(5):1326-1333. doi: 10.1053/j.gastro.2019.12.032. Epub 2020 Jan 8. Gastroenterology. 2020. PMID: 31926173
33 results