Forskning
Udskriv Udskriv
Switch language
Region Hovedstaden - en del af Københavns Universitetshospital

Hereditary Cancer in Clinical Practice, ‎1731-2302

Tidsskrift

  1. 2021
  2. Udgivet

    Danish guidelines for management of non-APC-associated hereditary polyposis syndromes

    Jelsig, A. M., Karstensen, J. G., Jespersen, N., Ketabi, Z., Lautrup, C., Rønlund, K., Sunde, L., Wadt, K., Thorlacius-Ussing, O. & Qvist, N., 7 okt. 2021, I: Hereditary Cancer in Clinical Practice. 19, 1, 41.

    Publikation: Bidrag til tidsskriftReviewForskningpeer review

  3. 2020
  4. Udgivet
  5. 2019
  6. Udgivet

    Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

    Seppälä, T. T., Ahadova, A., Dominguez-Valentin, M., Macrae, F., Evans, D. G., Therkildsen, C., Sampson, J., Scott, R., Burn, J., Möslein, G., Bernstein, I., Holinski-Feder, E., Pylvänäinen, K., Renkonen-Sinisalo, L., Lepistö, A., Lautrup, C. K., Lindblom, A., Plazzer, J-P., Winship, I., Tjandra, D., Katz, L. H., Aretz, S., Hüneburg, R., Holzapfel, S., Heinimann, K., Valle, A. D., Neffa, F., Gluck, N., de Vos Tot Nederveen Cappel, W. H., Vasen, H., Morak, M., Steinke-Lange, V., Engel, C., Rahner, N., Schmiegel, W., Vangala, D., Thomas, H., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Capella, G., Pineda, M., Navarro, M., Blanco, I., Ten Broeke, S., Nielsen, M., Ljungmann, K., Nakken, S., Lindor, N., Frayling, I., Hovig, E., Sunde, L., Kloor, M., Mecklin, J-P., Kalager, M. & Møller, P., 28 feb. 2019, I: Hereditary Cancer in Clinical Practice. 17, 1, s. 8 8.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  7. 2017
  8. Udgivet

    Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

    Seppälä, T., Pylvänäinen, K., Evans, D. G., Järvinen, H., Renkonen-Sinisalo, L., Bernstein, I., Holinski-Feder, E., Sala, P., Lindblom, A., Macrae, F., Blanco, I., Sijmons, R., Jeffries, J., Vasen, H., Burn, J., Nakken, S., Hovig, E., Rødland, E. A., Tharmaratnam, K., de Vos Tot Nederveen Cappel, W. H., Hill, J. O., Wijnen, J., Jenkins, M., Genuardi, M., Green, K., Lalloo, F., Sunde, L., Mints, M., Bertario, L., Pineda, M., Navarro, M., Morak, M., Frayling, I. M., Plazzer, J-P., Sampson, J. R., Capellá, G., Möslein, G., Mecklin, J-P., Møller, P. & Mallorca Group, 1 okt. 2017, I: Hereditary Cancer in Clinical Practice. 15, 18

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  9. 2016
  10. Udgivet

    Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients

    Bennedbæk, M., Rossing, M., Rasmussen, Å. K., Gerdes, A-M., Skytte, A-B., Jensen, U. B., Nielsen, F. C. & Hansen, T. V. O., 2016, I: Hereditary Cancer in Clinical Practice. 14, s. 13

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  11. 2013
  12. Udgivet

    Mutation spectrum in South American Lynch syndrome families

    Dominguez-Valentin, M., Nilbert, M., Wernhoff, P., López-Köstner, F., Vaccaro, C., Sarroca, C., Palmero, E. I., Giraldo, A., Ashton-Prolla, P., Alvarez, K., Ferro, A., Neffa, F., Caris, J., Carraro, D. M. & Rossi, B. M., 2013, I: Hereditary Cancer in Clinical Practice. 11, 1, s. 18

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  13. Udgivet

    Sense of coherence and self-concept in Lynch syndrome

    Petersen, H. V., Ladelund, S., Carlsson, C. & Nilbert, M., 2013, I: Hereditary Cancer in Clinical Practice. 11, 1, s. 7

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  14. 2012
  15. Udgivet

    Family perspectives in lynch syndrome becoming a family at risk, patterns of communication and influence on relations

    Bartuma, K., Nilbert, M. & Carlsson, C., 2012, I: Hereditary Cancer in Clinical Practice. 10, 1, s. 6

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

ID: 159383