Ethics and biobanks von Hansson, M G

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Hope for a cure and altruism are the main motives behind participation in phase 3 clinical cancer trials von Godskesen, T., Hansson, M.G., Nygren, P., Nordin, K., Kihlbom, U.

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Building on relationships of trust in biobank research von Hansson, M G

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The Swedish CArdioPulmonary BioImage Study: objectives and design von Bergström, G., Berglund, G., Blomberg, A., Brandberg, J., Engström, G., Engvall, J., Eriksson, M., Faire, U., Flinck, A., Hansson, M. G., Hedblad, B., Hjelmgren, O., Janson, C., Jernberg, T., Johnsson, Å., Johansson, L., Lind, L., Löfdahl, C.‐G., Melander, O., Östgren, C. J., Persson, A., Persson, M., Sandström, A., Schmidt, C., Söderberg, S., Sundström, J., Toren, K., Waldenström, A., Wedel, H., Vikgren, J., Fagerberg, B., Rosengren, A.

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A model of study for human cancer: Spontaneous occurring tumors in dogs. Biological features and translation for new anticancer therapies von Ranieri, G, Gadaleta, C.D, Patruno, R, Zizzo, N, Daidone, M.G, Hansson, M.G, Paradiso, A, Ribatti, D

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Split views among parents regarding children’s right to decide about participation in research: a questionnaire survey von Swartling, U, Helgesson, G, Hansson, M G, Ludvigsson, J

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Is medical ethics doing its job? von Hansson, M. G., Chadwick, R.

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Patients’ refusal to consent to storage and use of samples in Swedish biobanks: cross sectional study von Johnsson, Linus, Hansson, Mats G, Eriksson, Stefan, Helgesson, Gert

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Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: A population-based study von KETTIS-LINDBLAD, ÅSA, RING, LENA, VIBERTH, EVA, HANSSON, MATS G.

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Opt-out from biobanks better respects patients’ autonomy von Johnsson, Linus, Hansson, Mats G, Eriksson, Stefan, Helgesson, Gert

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Patients' Perceptions of Their Relatives' Risk of Developing Rheumatoid Arthritis and of the Potential for Risk Communication, Prediction, and Modulation von Falahee, Marie, Simons, Gwenda, Buckley, Christopher D., Hansson, Mats, Stack, Rebecca J., Raza, Karim

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Need for a wider view of autonomy in epidemiological research von Hansson, Mats G

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Ethical Management of Hereditary Cancer Information von Hansson, Mats G.

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Biobank research: who benefits from individual consent? von Stjernschantz Forsberg, Joanna, Hansson, Mats G, Eriksson, Stefan

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Living with conflicts-ethical dilemmas and moral distress in the health care system von Kälvemark, Sofia, Höglund, Anna T, Hansson, Mats G, Westerholm, Peter, Arnetz, Bengt

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Is medical ethics doing its job?: Introduction: Is medical ethics doing its job? von Hansson, M. G., Chadwick, R.

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Should donors be allowed to give broad consent to future biobank research? von Hansson, Mats G, Dillner, Joakim, Bartram, Claus R, Carlson, Joyce A, Helgesson, Gert

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Quality of life in patients with multiple endocrine neoplasia type 1 (MEN 1) von Berglund, G, Lidén, A, Hansson, M G, Oberg, K, Sjöden, P O, Nordin, K

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Research participants’ preferences for receiving genetic risk information: a discrete choice experiment von Viberg Johansson, Jennifer, Langenskiöld, Sophie, Segerdahl, Pär, Hansson, Mats G., Hösterey, Ulrika Ugander, Gummesson, Anders, Veldwijk, Jorien

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Is medical ethics doing its job?: Introduction von Hansson, Mats G., Chadwick, R.

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