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Author Details
Full Name
Yann Le Cam
Affiliation
ORCID
Career Start Year
2012
Papers
23
H Index
12
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37308991
Patients, payers and developers of Orphan Medicinal Products: lessons learned from 10Â years' multi-stakeholder dialogue on improving access in Europe via MoCA.
Orphanet J Rare Dis
2023
35645285
Towards Achieving Equity and Innovation in Newborn Screening across Europe.
Int J Neonatal Screen
2022
33262444
Reply to E. Vicente et al.
Eur J Hum Genet
2021
33884523
Our greatest untapped resource: our patients.
J Community Genet
2021
34975469
Orphan Medicine Incentives: How to Address the Unmet Needs of Rare Disease Patients by Optimizing the European Orphan Medicinal Product Landscape Guiding Principles and Policy Proposals by the European Expert Group for Orphan Drug Incentives (OD Expert Group).
Front Pharmacol
2021
31527858
Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database.
Eur J Hum Genet
2020
29901216
Medicines Adaptive Pathways to Patients: Why, When, and How to Engage?
Clin Pharmacol Ther
2019
28796411
Progress in Rare Diseases Research 2010-2016: An IRDiRC Perspective.
Clin Transl Sci
2018
29911566
[French model for Europe and Europe as a model for France in the field of rare diseases].
Med Sci (Paris)
2018
29977052
The evolution of adaptiveness: balancing speed and evidence.
Nat Rev Drug Discov
2018
27782107
'IRDiRC Recognized Resources': a new mechanism to support scientists to conduct efficient, high-quality research for rare diseases.
Eur J Hum Genet
2017
28283046
Recommendations from the European Working Group for Value Assessment and Funding Processes in Rare Diseases (ORPH-VAL).
Orphanet J Rare Dis
2017
29158551
The International Rare Diseases Research Consortium: Policies and Guidelines to maximize impact.
Eur J Hum Genet
2017
29214566
Improved Diagnosis and Care for Rare Diseases through Implementation of Precision Public Health Framework.
Adv Exp Med Biol
2017
26929314
A model for active and healthy ageing with a rare genetic disease: cystic fibrosis.
Eur Respir J
2016
26911987
The context for the thematic grouping of rare diseases to facilitate the establishment of European Reference Networks.
Orphanet J Rare Dis
2016
25537360
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases.
Eur J Hum Genet
2015
25669457
From adaptive licensing to adaptive pathways: delivering a flexible life-span approach to bring new drugs to patients.
Clin Pharmacol Ther
2015
24513034
Accelerating development, registration and access to medicines for rare diseases in the European Union through adaptive approaches: features and perspectives.
Orphanet J Rare Dis
2014
24922305
European Reference Networks for Rare Diseases: the vision of patients.
Blood Transfus
2014
24503588
EUROPLAN: a project to support the development of national plans on rare diseases in Europe.
Public Health Genomics
2013
22258596
Leap year: Rare day to highlight rare diseases.
Nature
2012
23293582
Involvement of patient organisations in research and development of orphan drugs for rare diseases in europe.
Mol Syndromol
2012
1 - 23 of 23
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