New functionalities in Orphanet for orphan drugs, R&D and marketing authorisations to better serve the rare diseases community

Antzeko izenburuak

• Rare diseases research in Europe: an overview based on data from the Orphanet database
  nork: Martin, Natalia, et al.
  Argitaratua: (2010)
• Orphanet Journal of Rare Diseases: Launch Editorial
  nork: Aymé, Ségolène, et al.
  Argitaratua: (2006)
• The influence of the European paediatric regulation on marketing authorisation of orphan drugs for children
  nork: Kreeftmeijer-Vegter, Annemarie Rosan, et al.
  Argitaratua: (2014)
• Evolution of national and European policies in the field of rare diseases and their impact over the past five years
  nork: Rodwell, Charlotte, et al.
  Argitaratua: (2014)
• The European Union Committee of Experts on Rare Diseases: three productive years at the service of the rare disease community
  nork: Aymé, Ségolène, et al.
  Argitaratua: (2014)