Familial Cancer, 1389-9600

Tidskrift

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  1. 2019
  2. Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition

    Lindberg, L. J., Wegen-Haitsma, W., Ladelund, S., Smith-Hansen, L., Therkildsen, C., Bernstein, I. & Mef Nilbert, 2019, I : Familial Cancer. 18, 2, s. 183-191

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. 2018
  4. Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries

    Brédart, A., Kop, J. L., Antoniou, A. C., Cunningham, A. P., de Pauw, A., Tischkowitz, M., Hans Ehrencrona, Dolbeault, S., Robieux, L., Rhiem, K., Easton, D. F., Devilee, P., Stoppa-Lyonnet, D. & Schmutlzer, R., 2018, I : Familial Cancer. 17, 1, s. 31-41

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 2017
  6. Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

    Anna Rohlin, Rambech, E., Anders Kvist, Therese Törngren, Eiengård, F., Lundstam, U., Zagoras, T., Samuel Gebre-Medhin, Åke Borg, Björk, J., Mef Nilbert & Nordling, M., 2017 apr, I : Familial Cancer. 16, 2, s. 195-203

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. 2016
  8. No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families.

    Nielsen, H. R., Petersen, J., Krogh, L., Mef Nilbert & Skytte, A-B., 2016 okt, I : Familial Cancer. 15, 4, s. 523–528

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.

    Nielsen, H. R., Mef Nilbert, Petersen, J., Ladelund, S., Thomassen, M., Pedersen, I. S., Hansen, T. V. O., Skytte, A-B., Åke Borg & Therkildsen, C., 2016, I : Familial Cancer. 15, 4, s. 507-512

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. 2014
  11. Distinct gene expression profiles in ovarian cancer linked to Lynch syndrome.

    Jenny-Maria Jönsson, Bartuma, K., Dominguez, M., Katja Harbst, Ketabi, Z., Malander, S., Mats Jönsson, Ana Carneiro, Måsbäck, A., Göran B Jönsson & Mef Nilbert, 2014, I : Familial Cancer. 13, 4, s. 537-545

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. 2012
  13. Cancer risks and immunohistochemical profiles linked to the Danish MLH1 Lynch syndrome founder mutation

    Therkildsen, C., Isinger-Ekstrand, A., Ladelund, S., Nissen, A., Rambech, E., Bernstein, I. & Mef Nilbert, 2012, I : Familial Cancer. 11, 4, s. 579-585

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.

    Magnusson, S., Thomas Wiebe, Ulf Kristoffersson, Helena Jernström & Håkan Olsson, 2012, I : Familial Cancer. 11, s. 145-155

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. 2011
  16. Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals

    Dominguez, M., da Silva, F. C., Monteiro dos Santos, E. M., Lisboa, B. G., de Oliveira, L. P., Ferreira, F. D. O., Gomy, I., Nakagawa, W. T., Aguiar Junior, S., Redal, M., Vaccaro, C., Della Valle, A., Sarroca, C., Carraro, D. M. & Rossi, B. M., 2011, I : Familial Cancer. 10, 4, s. 641-647

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Therkildsen, C., Bernstein, I. & Mef Nilbert, 2011, I : Familial Cancer. 10, s. 239-243

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer

    Henningson, M., Hietala, M., Therese Törngren, Håkan Olsson & Helena Jernström, 2011, I : Familial Cancer. 10, 2, s. 173-185

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study

    Petersen, H. V., Esplen, M. J., Ladelund, S., Bernstein, I., Sunde, L., Christina Carlsson & Mef Nilbert, 2011, I : Familial Cancer. 10, 4, s. 633-639

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. 2010
  21. Can a phenotype for recessive inheritance in breast cancer be defined?

    Carolina Ellberg, Göran B Jönsson & Håkan Olsson, 2010, I : Familial Cancer. 9, 4, s. 525-530

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  22. Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Mats Jönsson, Lindblom, A., Åke Borg & Mef Nilbert, 2010, I : Familial Cancer. 9, s. 125-129

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. 2009
  24. Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

    Mef Nilbert, Therkildsen, C., Nissen, A., Åkerman, M. & Bernstein, I., 2009, I : Familial Cancer. 8, 3, s. 209-213

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  25. 2008
  26. 2007
  27. 2006
  28. The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer.

    Halvarsson, B., Lindblom, A., Rambech, E., Lagerstedt, K. & Mef Nilbert, 2006, I : Familial Cancer. 5, 4, s. 353-358

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. The added value of PMS2 staining for the diagnosis of hereditary nonpolyposis colorectal cancer

    Halvarsson, B., Mef Nilbert, Rambech, E. & Lindblom, A., 2006, I : Familial Cancer. 5, s. 353

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift