Apold J - Search Results

1

Surveillance for familial breast cancer: Differences in outcome according to BRCA mutation status.

Moller P, Evans DG, Reis MM, Gregory H, Anderson E, Maehle L, Lalloo F, Howell A, Apold J, Clark N, Lucassen A, Steel CM. Moller P, et al. Among authors: apold j. Int J Cancer. 2007 Sep 1;121(5):1017-20. doi: 10.1002/ijc.22789. Int J Cancer. 2007. PMID: 17471561

2

Survival in prospectively ascertained familial breast cancer: analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy.

Møller P, Borg A, Evans DG, Haites N, Reis MM, Vasen H, Anderson E, Steel CM, Apold J, Goudie D, Howell A, Lalloo F, Maehle L, Gregory H, Heimdal K. Møller P, et al. Among authors: apold j. Int J Cancer. 2002 Oct 20;101(6):555-9. doi: 10.1002/ijc.10641. Int J Cancer. 2002. PMID: 12237897

3

[Hereditary breast cancer].

Møller P, Maehle L, Apold J. Møller P, et al. Among authors: apold j. Tidsskr Nor Laegeforen. 2005 Nov 17;125(22):3136-8. Tidsskr Nor Laegeforen. 2005. PMID: 16299574 Free article. Norwegian.

4

Genetic epidemiology of BRCA mutations--family history detects less than 50% of the mutation carriers.

Møller P, Hagen AI, Apold J, Maehle L, Clark N, Fiane B, Løvslett K, Hovig E, Vabø A. Møller P, et al. Among authors: apold j. Eur J Cancer. 2007 Jul;43(11):1713-7. doi: 10.1016/j.ejca.2007.04.023. Epub 2007 Jun 15. Eur J Cancer. 2007. PMID: 17574839

5

High risk for ovarian cancer in a prospective series is restricted to BRCA1/2 mutation carriers.

Maehle L, Apold J, Paulsen T, Hagen B, Løvslett K, Fiane B, Van Ghelue M, Clark N, Møller P. Maehle L, et al. Among authors: apold j. Clin Cancer Res. 2008 Nov 15;14(22):7569-73. doi: 10.1158/1078-0432.CCR-08-0112. Clin Cancer Res. 2008. PMID: 19010876

6

No sib pair concordance for breast or ovarian cancer in BRCA1 mutation carriers.

Møller P, Maehle L, Clark N, Apold J. Møller P, et al. Among authors: apold j. Hered Cancer Clin Pract. 2007 Jun 15;5(2):67-71. doi: 10.1186/1897-4287-5-2-67. Hered Cancer Clin Pract. 2007. PMID: 19725986 Free PMC article.

7

The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer.

Heimdal K, Maehle L, Apold J, Pedersen JC, Møller P. Heimdal K, et al. Among authors: apold j. Eur J Cancer. 2003 Oct;39(15):2205-13. doi: 10.1016/s0959-8049(03)00548-3. Eur J Cancer. 2003. PMID: 14522380

8

Efficacy of early diagnosis and treatment in women with a family history of breast cancer. European Familial Breast Cancer Collaborative Group.

Møller P, Reis MM, Evans G, Vasen H, Haites N, Anderson E, Steel CM, Apold J, Lalloo F, Maehle L, Preece P, Gregory H, Heimdal K. Møller P, et al. Among authors: apold j. Dis Markers. 1999 Oct;15(1-3):179-86. doi: 10.1155/1999/805420. Dis Markers. 1999. PMID: 10595275 Free PMC article.

9

Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer.

Møller P, Evans G, Haites N, Vasen H, Reis MM, Anderson E, Apold J, Hodgson S, Eccles D, Olsson H, Stoppa-Lyonnet D, Chang-Claude J, Morrison PJ, Bevilacqua G, Heimdal K, Maehle L, Lalloo F, Gregory H, Preece P, Borg A, Nevin NC, Caligo M, Steel CM. Møller P, et al. Among authors: apold j. Dis Markers. 1999 Oct;15(1-3):207-11. doi: 10.1155/1999/920109. Dis Markers. 1999. PMID: 10595280 Free PMC article. Review.

10

[Handling of hereditary intestinal cancer].

Møller P, Stormorken A, Apold J. Møller P, et al. Among authors: apold j. Tidsskr Nor Laegeforen. 2006 Aug 10;126(15):1937-9. Tidsskr Nor Laegeforen. 2006. PMID: 16915319 Free article. Norwegian.

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