Hoogerbrugge N - Search Results

1

More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.

Sie AS, van Zelst-Stams WA, Spruijt L, Mensenkamp AR, Ligtenberg MJ, Brunner HG, Prins JB, Hoogerbrugge N. Sie AS, et al. Among authors: hoogerbrugge n. Fam Cancer. 2014 Jun;13(2):143-51. doi: 10.1007/s10689-013-9686-z. Fam Cancer. 2014. PMID: 24068317

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

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.

Oldenburg RA, Kroeze-Jansema K, Kraan J, Morreau H, Klijn JG, Hoogerbrugge N, Ligtenberg MJ, van Asperen CJ, Vasen HF, Meijers C, Meijers-Heijboer H, de Bock TH, Cornelisse CJ, Devilee P. Oldenburg RA, et al. Among authors: hoogerbrugge n. Cancer Res. 2003 Dec 1;63(23):8153-7. Cancer Res. 2003. PMID: 14678969

5

Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: hoogerbrugge n. Br J Cancer. 2004 Jan 26;90(2):333-42. doi: 10.1038/sj.bjc.6601525. Br J Cancer. 2004. PMID: 14735173 Free PMC article. Clinical Trial.

6

Impact of BRCA1/2 testing and disclosure of a positive test result on women affected and unaffected with breast or ovarian cancer.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: hoogerbrugge n. Am J Med Genet A. 2004 Feb 1;124A(4):346-55. doi: 10.1002/ajmg.a.20374. Am J Med Genet A. 2004. PMID: 14735581 Free article.

7

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. Among authors: hoogerbrugge n. Clin Genet. 2004 Apr;65(4):308-16. doi: 10.1111/j.1399-0004.2004.00220.x. Clin Genet. 2004. PMID: 15025724

8

More differences between HNPCC-related and sporadic carcinomas from the endometrium as compared to the colon.

van den Bos M, van den Hoven M, Jongejan E, van der Leij F, Michels M, Schakenraad S, Aben K, Hoogerbrugge N, Ligtenberg M, van Krieken JH. van den Bos M, et al. Among authors: hoogerbrugge n. Am J Surg Pathol. 2004 Jun;28(6):706-11. doi: 10.1097/01.pas.0000126720.49083.11. Am J Surg Pathol. 2004. PMID: 15166662

9

Randomized trial of a shared decision-making intervention consisting of trade-offs and individualized treatment information for BRCA1/2 mutation carriers.

van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, Moog U, van Daal WA. van Roosmalen MS, et al. Among authors: hoogerbrugge n. J Clin Oncol. 2004 Aug 15;22(16):3293-301. doi: 10.1200/JCO.2004.05.066. J Clin Oncol. 2004. PMID: 15310772 Free article. Clinical Trial.

10

[In cases of familial ovarian cancer, always consider the risk of breast cancer].

Kets CM, Niermeijer MF, Massuger LF, Hoogerbrugge N. Kets CM, et al. Among authors: hoogerbrugge n. Ned Tijdschr Geneeskd. 2004 Aug 28;148(35):1709-11. Ned Tijdschr Geneeskd. 2004. PMID: 15468897 Dutch.

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