Møller P - Search Results

1

[Retinoblastoma--hereditary eye cancer in children?].

Møller P, Apold J. Møller P, et al. Tidsskr Nor Laegeforen. 2004 Mar 18;124(6):830; author reply 830. Tidsskr Nor Laegeforen. 2004. PMID: 15039827 Free article. Norwegian. No abstract available.

2

[Hereditary breast cancer].

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

3

[Handling of hereditary intestinal cancer].

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

4

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. Int J Cancer. 2002 Oct 20;101(6):555-9. doi: 10.1002/ijc.10641. Int J Cancer. 2002. PMID: 12237897 Free article.

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: moller p. 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

Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer.

Stormorken AT, Bowitz-Lothe IM, Norèn T, Kure E, Aase S, Wijnen J, Apold J, Heimdal K, Møller P. Stormorken AT, et al. Among authors: moller p. J Clin Oncol. 2005 Jul 20;23(21):4705-12. doi: 10.1200/JCO.2005.05.180. J Clin Oncol. 2005. PMID: 16034045

7

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. Int J Cancer. 2007 Sep 1;121(5):1017-20. doi: 10.1002/ijc.22789. Int J Cancer. 2007. PMID: 17471561 Free article.

8

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. 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

9

Sensitivity of MRI versus conventional screening in the diagnosis of BRCA-associated breast cancer in a national prospective series.

Hagen AI, Kvistad KA, Maehle L, Holmen MM, Aase H, Styr B, Vabø A, Apold J, Skaane P, Møller P. Hagen AI, et al. Among authors: moller p. Breast. 2007 Aug;16(4):367-74. doi: 10.1016/j.breast.2007.01.006. Epub 2007 Feb 21. Breast. 2007. PMID: 17317184 Clinical Trial.

10

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations.

Rudkin TM, Hamel N, Galvez M, Hogervorst F, Gille JJ, Møller P, Apold J, Foulkes WD. Rudkin TM, et al. Among authors: moller p. BMC Med Genet. 2006 Mar 1;7:15. doi: 10.1186/1471-2350-7-15. BMC Med Genet. 2006. PMID: 16509964 Free PMC article.

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