Ligtenberg MJL - Search Results

1

Microsatellite instability screening in colorectal adenomas to detect Lynch syndrome patients? A systematic review and meta-analysis.

Dabir PD, Bruggeling CE, van der Post RS, Dutilh BE, Hoogerbrugge N, Ligtenberg MJL, Boleij A, Nagtegaal ID. Dabir PD, et al. Among authors: ligtenberg mjl. Eur J Hum Genet. 2020 Mar;28(3):277-286. doi: 10.1038/s41431-019-0538-7. Epub 2019 Nov 6. Eur J Hum Genet. 2020. PMID: 31695176 Free PMC article.

2

High prevalence of premalignant lesions in prophylactically removed breasts from women at hereditary risk for breast cancer.

Hoogerbrugge N, Bult P, de Widt-Levert LM, Beex LV, Kiemeney LA, Ligtenberg MJ, Massuger LF, Boetes C, Manders P, Brunner HG. Hoogerbrugge N, et al. J Clin Oncol. 2003 Jan 1;21(1):41-5. doi: 10.1200/JCO.2003.02.137. J Clin Oncol. 2003. PMID: 12506168 Free article.

3

Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCC.

Hoogerbrugge N, Willems R, Van Krieken HJ, Kiemeney LA, Weijmans M, Nagengast FM, Arts N, Brunner HG, Ligtenberg MJ. Hoogerbrugge N, et al. Clin Genet. 2003 Jan;63(1):64-70. doi: 10.1034/j.1399-0004.2003.630110.x. Clin Genet. 2003. PMID: 12519374

4

Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysis.

Kievit W, de Bruin JH, Adang EM, Ligtenberg MJ, Nagengast FM, van Krieken JH, Hoogerbrugge N. Kievit W, et al. Clin Genet. 2004 Apr;65(4):308-16. doi: 10.1111/j.1399-0004.2004.00220.x. Clin Genet. 2004. PMID: 15025724

5

[Recognising hereditary non-polyposis colorectal cancer without a clear family history].

de Bruin JH, Nagengast FM, Ligtenberg MJ, van Krieken JH, Niermeijer MF, Hoogerbrugge N. de Bruin JH, et al. Ned Tijdschr Geneeskd. 2004 Oct 16;148(42):2053-7. Ned Tijdschr Geneeskd. 2004. PMID: 15532325 Dutch.

6

Cost effectiveness of a new strategy to identify HNPCC patients.

Kievit W, de Bruin JH, Adang EM, Severens JL, Kleibeuker JH, Sijmons RH, Ruers TJ, Nagengast FM, Vasen HF, van Krieken JH, Ligtenberg MJ, Hoogerbrugge N. Kievit W, et al. Gut. 2005 Jan;54(1):97-102. doi: 10.1136/gut.2004.039123. Gut. 2005. PMID: 15591512 Free PMC article.

7

Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.

Leegte B, van der Hout AH, Deffenbaugh AM, Bakker MK, Mulder IM, ten Berge A, Leenders EP, Wesseling J, de Hullu J, Hoogerbrugge N, Ligtenberg MJ, Ardern-Jones A, Bancroft E, Salmon A, Barwell J, Eeles R, Oosterwijk JC. Leegte B, et al. J Med Genet. 2005 Mar;42(3):e20. doi: 10.1136/jmg.2004.027243. J Med Genet. 2005. PMID: 15744030 Free PMC article. Review. No abstract available.

8

[More hereditary intestinal cancer can be detected if patients with colorectal carcinoma that are selected by the pathologist are examined for microsatellite instability].

de Bruin JH, Kievit W, Ligtenberg MJ, Nagengast FM, Adang EM, Ruers TJ, Kleibeuker JH, Sijmons RH, van Krieken JH, Hoogerbrugge N. de Bruin JH, et al. Ned Tijdschr Geneeskd. 2005 Aug 6;149(32):1792-8. Ned Tijdschr Geneeskd. 2005. PMID: 16121665 Dutch.

9

MUTYH and the mismatch repair system: partners in crime?

Niessen RC, Sijmons RH, Ou J, Olthof SG, Osinga J, Ligtenberg MJ, Hogervorst FB, Weiss MM, Tops CM, Hes FJ, de Bock GH, Buys CH, Kleibeuker JH, Hofstra RM. Niessen RC, et al. Hum Genet. 2006 Mar;119(1-2):206-11. doi: 10.1007/s00439-005-0118-5. Epub 2006 Jan 12. Hum Genet. 2006. PMID: 16408224

10

Surveillance of women at high risk for hereditary ovarian cancer is inefficient.

Oei AL, Massuger LF, Bulten J, Ligtenberg MJ, Hoogerbrugge N, de Hullu JA. Oei AL, et al. Br J Cancer. 2006 Mar 27;94(6):814-9. doi: 10.1038/sj.bjc.6603015. Br J Cancer. 2006. PMID: 16495917 Free PMC article.

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