Prioritizing treatment of rare diseases: A survey of preferences of Norwegian doctors
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DOI: 10.1016/j.socscimed.2013.06.019
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- Cookson, Richard & Dolan, Paul, 1999. "Public views on health care rationing: a group discussion study," Health Policy, Elsevier, vol. 49(1-2), pages 63-74, September.
- Mentzakis, Emmanouil & Stefanowska, Patricia & Hurley, Jeremiah, 2011. "A discrete choice experiment investigating preferences for funding drugs used to treat orphan diseases: an exploratory study," Health Economics, Policy and Law, Cambridge University Press, vol. 6(3), pages 405-433, July.
- Nord, Erik & Richardson, Jeff & Street, Andrew & Kuhse, Helga & Singer, Peter, 1995. "Maximizing health benefits vs egalitarianism: An Australian survey of health issues," Social Science & Medicine, Elsevier, vol. 41(10), pages 1429-1437, November.
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- Douglas A. Coyle & Matthew C. Cheung & Gerald A. Evans, 2015. "The Need for Transparency and Efficiency in Reimbursement Decisions Relating to Drugs for Rare Diseases," Medical Decision Making, , vol. 35(2), pages 145-147, February.
- Oriol de Sola-Morales, 2019. "Funding orphan medicinal products beyond price: sustaining an ecosystem," The European Journal of Health Economics, Springer;Deutsche Gesellschaft für Gesundheitsökonomie (DGGÖ), vol. 20(9), pages 1283-1286, December.
- Hirokuni Mizoguchi & Shingo Kano, 2019. "Comparative analysis of correlations of research and development indicators for rare diseases among Japan, the US, and Europe," Scientometrics, Springer;Akadémiai Kiadó, vol. 120(2), pages 361-374, August.
- Kleinhout-Vliek, Tineke & de Bont, Antoinette & Boer, Bert, 2017. "The bare necessities? A realist review of necessity argumentations used in health care coverage decisions," Health Policy, Elsevier, vol. 121(7), pages 731-744.
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Keywords
Norway; Rare diseases; Priority setting; Doctor preferences; Societal preferences; Orphan drugs;All these keywords.
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