Møller P - Search Results

1

BRCA1 1675delA and 1135insA account for one third of Norwegian familial breast-ovarian cancer and are associated with later disease onset than less frequent mutations.

Borg A, Dørum A, Heimdal K, Maehle L, Hovig E, Møller P. Borg A, et al. Among authors: moller p. Dis Markers. 1999 Oct;15(1-3):79-84. doi: 10.1155/1999/278269. Dis Markers. 1999. PMID: 10595257 Free PMC article.

2

Penetrances of BRCA1 1675delA and 1135insA with respect to breast cancer and ovarian cancer.

Dørum A, Heimdal K, Hovig E, Inganäs M, Møller P. Dørum A, et al. Among authors: moller p. Am J Hum Genet. 1999 Sep;65(3):671-9. doi: 10.1086/302530. Am J Hum Genet. 1999. PMID: 10441573 Free PMC article.

3

Uptake of genetic testing and pre-test levels of mental distress in Norwegian families with known BRCA1 mutations.

Reichelt JG, Dahl AA, Heimdal K, Møller P. Reichelt JG, et al. Among authors: moller p. Dis Markers. 1999 Oct;15(1-3):139-43. doi: 10.1155/1999/581346. Dis Markers. 1999. PMID: 10595268 Free PMC article.

4

Costs and benefits of diagnosing familial breast cancer.

Heimdal K, Maehle L, Møller P. Heimdal K, et al. Among authors: moller p. Dis Markers. 1999 Oct;15(1-3):167-73. doi: 10.1155/1999/751892. Dis Markers. 1999. PMID: 10595273 Free PMC article.

5

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. Dis Markers. 1999 Oct;15(1-3):179-86. doi: 10.1155/1999/805420. Dis Markers. 1999. PMID: 10595275 Free PMC article.

6

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. Dis Markers. 1999 Oct;15(1-3):207-11. doi: 10.1155/1999/920109. Dis Markers. 1999. PMID: 10595280 Free PMC article. Review.

7

Early detection of familial ovarian cancer.

Dørum A, Kristensen GB, Abeler VM, Tropé CG, Møller P. Dørum A, et al. Among authors: moller p. Eur J Cancer. 1996 Sep;32A(10):1645-51. doi: 10.1016/0959-8049(96)00137-2. Eur J Cancer. 1996. PMID: 8983269 Clinical Trial.

8

The problem of skipped generation and subclinical disease in familial breast-ovarian cancer.

Dørum A, Abeler VM, Heimdal K, Tropé C, Møller P. Dørum A, et al. Among authors: moller p. Acta Obstet Gynecol Scand. 1997 Feb;76(2):166-8. doi: 10.3109/00016349709050074. Acta Obstet Gynecol Scand. 1997. PMID: 9049291 Free article.

9

Inherited breast carcinoma--prospective findings in 1,194 women at risk.

Møller P, Maehle L, Heimdal K, Dørum A, Tretli S, Helgerud P, Quist H, Bjørndal H, Kåresen R, Nysted A, Varhaug JE, Fjøsne HE, Guleng RJ, Due J, Bøhler P, Giercksky KE, Tropé C, Kvinnsland S. Møller P, et al. Acta Oncol. 1996;35 Suppl 8:7-11. doi: 10.3109/02841869609098515. Acta Oncol. 1996. PMID: 9073043

10

A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing.

Dørum A, Møller P, Kamsteeg EJ, Scheffer H, Burton M, Heimdal KR, Maehle LO, Hovig E, Tropé CG, van der Hout AH, van der Meulen MA, Buys CH, te Meerman GJ. Dørum A, et al. Among authors: moller p. Eur J Cancer. 1997 Dec;33(14):2390-2. doi: 10.1016/s0959-8049(97)00328-6. Eur J Cancer. 1997. PMID: 9616287

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