Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Nicod, Elena
Berg Brigham, Karen
Durand-Zaleski, Isabelle
and
Kanavos, Panos
2017.
Dealing with Uncertainty and Accounting for Social Value Judgments in Assessments of Orphan Drugs: Evidence from Four European Countries.
Value in Health,
Vol. 20,
Issue. 7,
p.
919.
Angelis, Aris
Kanavos, Panos
and
Montibeller, Gilberto
2017.
Resource Allocation and Priority Setting in Health Care: A Multi‐criteria Decision Analysis Problem of Value?.
Global Policy,
Vol. 8,
Issue. S2,
p.
76.
Young, Katherine Eve
Soussi, Imen
Hemels, Michiel
and
Toumi, Mondher
2017.
A comparative study of orphan drug prices in Europe.
Journal of Market Access & Health Policy,
Vol. 5,
Issue. 1,
p.
1297886.
de Folter, Joost
Trusheim, Mark
Jonsson, Pall
and
Garner, Sarah
2018.
DECISION-COMPONENTS OF NICE'S TECHNOLOGY APPRAISALS ASSESSMENT FRAMEWORK.
International Journal of Technology Assessment in Health Care,
Vol. 34,
Issue. 2,
p.
163.
Cannizzo, Sara
Lorenzoni, Valentina
Palla, Ilaria
Pirri, Salvatore
Trieste, Leopoldo
Triulzi, Isotta
and
Turchetti, Giuseppe
2018.
Rare diseases under different levels of economic analysis: current activities, challenges and perspectives.
RMD Open,
Vol. 4,
Issue. Suppl 1,
p.
e000794.
Kamusheva, Maria
Tachkov, Konstantin
Petrova, Guenka
Savova, Alexandra
and
Manova, Manoela
2018.
Orphan medicinal products’ access to the Bulgarian pharmaceutical market – challenges and obstacles.
Expert Opinion on Orphan Drugs,
Vol. 6,
Issue. 2,
p.
95.
Tervonen, Tommi
Angelis, Aris
Hockley, Kimberley
Pignatti, Francesco
and
Phillips, Lawrence D.
2019.
Quantifying Preferences in Drug Benefit‐Risk Decisions.
Clinical Pharmacology & Therapeutics,
Vol. 106,
Issue. 5,
p.
955.
Somers, Camilla
Chimonas, Susan
McIntosh, Emma
Kaltenboeck, Anna
Briggs, Andrew
and
Bach, Peter
2019.
Using Nominal Group Technique to Identify Key Attributes of Oncology Treatments for a Discrete Choice Experiment.
MDM Policy & Practice,
Vol. 4,
Issue. 1,
Lasalvia, P
Prieto-Pinto, L
Moreno, M
Castrillón, J
Romano, G
Garzón-Orjuela, N
and
Rosselli, D
2019.
International experiences in multicriteria decision analysis (MCDA) for evaluating orphan drugs: a scoping review.
Expert Review of Pharmacoeconomics & Outcomes Research,
Vol. 19,
Issue. 4,
p.
409.
Contesse, Marielle G.
Valentine, James E.
Wall, Tracy E.
and
Leffler, Mindy G.
2019.
The Case for the Use of Patient and Caregiver Perception of Change Assessments in Rare Disease Clinical Trials: A Methodologic Overview.
Advances in Therapy,
Vol. 36,
Issue. 5,
p.
997.
Wagner, Monika
Samaha, Dima
Casciano, Roman
Brougham, Matthew
Abrishami, Payam
Petrie, Charles
Avouac, Bernard
Mantovani, Lorenzo
Sarría-Santamera, Antonio
Kind, Paul
Schlander, Michael
and
Tringali, Michele
2019.
Moving Towards Accountability for Reasonableness – A Systematic Exploration of the Features of Legitimate Healthcare Coverage Decision-Making Processes Using Rare Diseases and Regenerative Therapies as a Case Study.
International Journal of Health Policy and Management,
Vol. 8,
Issue. 7,
p.
424.
Wranik, Wiesława Dominika
Jakubczyk, Michał
and
Drachal, Krzysztof
2020.
Ranking the Criteria Used in the Appraisal of Drugs for Reimbursement: A Stated Preferences Elicitation With Health Technology Assessment Stakeholders Across Jurisdictional Contexts.
Value in Health,
Vol. 23,
Issue. 4,
p.
471.
Bauer, Annette
Wittenberg, Raphael
Ly, Amanda
Gustavsson, Anders
Bexelius, Christin
Tochel, Claire
Knapp, Martin
Nelson, Mia
and
Sudlow, Catherine
2020.
Valuing Alzheimer's disease drugs: a health technology assessment perspective on outcomes.
International Journal of Technology Assessment in Health Care,
Vol. 36,
Issue. 4,
p.
297.
Nicod, Elena
Whittal, Amanda
Drummond, Michael
and
Facey, Karen
2020.
Are supplemental appraisal/reimbursement processes needed for rare disease treatments? An international comparison of country approaches.
Orphanet Journal of Rare Diseases,
Vol. 15,
Issue. 1,
Nicod, Elena
Maynou, Laia
Visintin, Erica
and
Cairns, John
2020.
Why do health technology assessment drug reimbursement recommendations differ between countries? A parallel convergent mixed methods study.
Health Economics, Policy and Law,
Vol. 15,
Issue. 3,
p.
386.
Zimmermann, Bettina M.
Eichinger, Johanna
and
Baumgartner, Matthias R.
2021.
A systematic review of moral reasons on orphan drug reimbursement.
Orphanet Journal of Rare Diseases,
Vol. 16,
Issue. 1,
Efthymiadou, Olina
and
Kanavos, Panos
2021.
Determinants of Managed Entry Agreements in the context of Health Technology Assessment: a comparative analysis of oncology therapies in four countries.
International Journal of Technology Assessment in Health Care,
Vol. 37,
Issue. 1,
Sarri, Grammati
Freitag, Andreas
Szegvari, Boglarka
Mountian, Irina
Brixner, Diana
Bertelsen, Neil
Kaló, Zoltán
and
Upadhyaya, Sheela
2021.
The Role of Patient Experience in the Value Assessment of Complex Technologies – Do HTA Bodies Need to Reconsider How Value is Assessed?.
Health Policy,
Vol. 125,
Issue. 5,
p.
593.
Vandewalle, Björn
Amorim, Miguel
Ramos, Diogo
Azevedo, Sofia
Alves, Inês
Francisco, Telma
Pinto, Helena
and
Sousa, Sérgio
2021.
Value-based decision-making for orphan drugs with multiple criteria decision analysis: burosumab for the treatment of X-linked hypophosphatemia.
Current Medical Research and Opinion,
Vol. 37,
Issue. 6,
p.
1021.
Charlton, Victoria
2022.
Does NICE apply the rule of rescue in its approach to highly specialised technologies?.
Journal of Medical Ethics,
Vol. 48,
Issue. 2,
p.
118.