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

Year Number of Results
1995 1
1999 1
2000 1
2001 1
2003 2
2005 1
2006 1
2007 1
2009 4
2010 9
2011 9
2012 7
2013 3
2014 4
2015 3
2016 1
2021 0
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40 results
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Page 1
International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer.
Canto MI, Harinck F, Hruban RH, Offerhaus GJ, Poley JW, Kamel I, Nio Y, Schulick RS, Bassi C, Kluijt I, Levy MJ, Chak A, Fockens P, Goggins M, Bruno M; International Cancer of Pancreas Screening (CAPS) Consortium. Canto MI, et al. Among authors: kluijt i. Gut. 2013 Mar;62(3):339-47. doi: 10.1136/gutjnl-2012-303108. Epub 2012 Nov 7. Gut. 2013. PMID: 23135763 Free PMC article.
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.
Ruijs MW, Verhoef S, Rookus MA, Pruntel R, van der Hout AH, Hogervorst FB, Kluijt I, Sijmons RH, Aalfs CM, Wagner A, Ausems MG, Hoogerbrugge N, van Asperen CJ, Gomez Garcia EB, Meijers-Heijboer H, Ten Kate LP, Menko FH, van 't Veer LJ. Ruijs MW, et al. Among authors: kluijt i. J Med Genet. 2010 Jun;47(6):421-8. doi: 10.1136/jmg.2009.073429. J Med Genet. 2010. PMID: 20522432 Free article.
Birt-Hogg-Dubé Syndrome.
Reese E, Sluzevich J, Kluijt I, Teertstra HJ, De Jong D, Horenblas S, Ryu J. Reese E, et al. Among authors: kluijt i. 2009 Sep 1 [updated 2009 Oct 5]. In: Riegert-Johnson DL, Boardman LA, Hefferon T, Roberts M, editors. Cancer Syndromes [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2009–. 2009 Sep 1 [updated 2009 Oct 5]. In: Riegert-Johnson DL, Boardman LA, Hefferon T, Roberts M, editors. Cancer Syndromes [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2009–. PMID: 21249760 Free Books & Documents. Review.
Hereditary causes of kidney tumours.
Axwijk PH, Kluijt I, de Jong D, Gille H, Teertstra J, Horenblas S. Axwijk PH, et al. Among authors: kluijt i. Eur J Clin Invest. 2010 May;40(5):433-9. doi: 10.1111/j.1365-2362.2010.02270.x. Eur J Clin Invest. 2010. PMID: 20534065 Review.
An α-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer.
Majewski IJ, Kluijt I, Cats A, Scerri TS, de Jong D, Kluin RJ, Hansford S, Hogervorst FB, Bosma AJ, Hofland I, Winter M, Huntsman D, Jonkers J, Bahlo M, Bernards R. Majewski IJ, et al. Among authors: kluijt i. J Pathol. 2013 Mar;229(4):621-9. doi: 10.1002/path.4152. J Pathol. 2013. PMID: 23208944
Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence.
Tan-Sindhunata MB, Mathijssen IB, Smit M, Baas F, de Vries JI, van der Voorn JP, Kluijt I, Hagen MA, Blom EW, Sistermans E, Meijers-Heijboer H, Waisfisz Q, Weiss MM, Groffen AJ. Tan-Sindhunata MB, et al. Among authors: kluijt i. Eur J Hum Genet. 2015 Sep;23(9):1151-7. doi: 10.1038/ejhg.2014.273. Epub 2014 Dec 24. Eur J Hum Genet. 2015. PMID: 25537362 Free PMC article.
Ataxia telangiectasia: the consequences of a delayed diagnosis.
Mandigers CM, van de Warrenburg BP, Strobbe LJ, Kluijt I, Molenaar AH, Schinagl DA. Mandigers CM, et al. Among authors: kluijt i. Radiother Oncol. 2011 Apr;99(1):97-8. doi: 10.1016/j.radonc.2011.02.007. Epub 2011 Feb 26. Radiother Oncol. 2011. PMID: 21354641 No abstract available.
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