Setting up strategies: patient inclusion in biobank and genomics research in Europe

Lignende værker

• Cell therapies for Duchenne muscular dystrophy: some ethical issues for personalised medicines
  af: McCormack, Pauline
  Udgivet: (2010)
• ‘You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research
  af: McCormack, Pauline, et al.
  Udgivet: (2016)
• Rapid set up of research centres in a trial in an evolving research governance world
  af: Ruddock, Sharon, et al.
  Udgivet: (2013)
• New Recommendation on Biological Materials Could Hamper Muscular Dystrophy Research
  af: McCormack, Pauline, et al.
  Udgivet: (2016)
• "Ready, set, go" - are we facilitating change in the (pre-) contemplative clinician?
  af: O'Sullivan, Ulrike, et al.
  Udgivet: (2014)