Rare Diseases: Canada's "research Orphans"
Overview
Overview
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Authors
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Affiliations
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Citing Articles
Rawson N Orphanet J Rare Dis. 2017; 12(1):59.
PMID: 28330479 PMC: 5363033. DOI: 10.1186/s13023-017-0611-7.
Value-based reimbursement decisions for orphan drugs: a scoping review and decision framework.
Paulden M, Stafinski T, Menon D, McCabe C Pharmacoeconomics. 2014; 33(3):255-69.
PMID: 25412735 PMC: 4342524. DOI: 10.1007/s40273-014-0235-x.
References
1.
Rados C
. Orphan products: hope for people with rare diseases. FDA Consum. 2004; 37(6):10-5.
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2.
Gericke C, Riesberg A, Busse R
. Ethical issues in funding orphan drug research and development. J Med Ethics. 2005; 31(3):164-8.
PMC: 1734115.
DOI: 10.1136/jme.2003.007138.
View
3.
Taruscio D, Vittozzi L, Stefanov R
. National plans and strategies on rare diseases in Europe. Adv Exp Med Biol. 2010; 686:475-91.
DOI: 10.1007/978-90-481-9485-8_26.
View
4.
Lavandeira A
. Orphan drugs: legal aspects, current situation. Haemophilia. 2002; 8(3):194-8.
DOI: 10.1046/j.1365-2516.2002.00643.x.
View
5.
Haffner M
. Adopting orphan drugs--two dozen years of treating rare diseases. N Engl J Med. 2006; 354(5):445-7.
DOI: 10.1056/NEJMp058317.
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