Browsing publications by Dr Pauline McCormack

Newcastle AuthorsTitleYearFull text
Dr Pauline McCormack
Dr Simon Woods
Consent, collaboration and cures:the views of rare disease patients on systems for sharing data and biospecimens2015
Dr Pauline McCormack
Dr Simon Woods
Professor Hanns Lochmuller
International Charter of principles for sharing bio-specimens and data2014
Dr Matthias Wienroth
Dr Pauline McCormack
Precaution, governance and the failure of medical implants: the ASR(TM) hip in the UK2014
Dr Pauline McCormack
Setting up strategies: patient inclusion in biobank and genomics research in Europe2014
Dr Simon Woods
Dr Pauline McCormack
Therapeutic Misconception: Hope, Trust and Misconception in Paediatric Research2014
Dr Pauline McCormack
Dr Matthias Wienroth
Clare Hopkins
Professor Tom Joyce
A mile in my shoes: the experiences of ASR hip patients and their families2013
Dr Simon Woods
Dr Pauline McCormack
Disputing the ethics of research: the challenge from bioethics and patient activism to the interpretation of the Declaration of Helsinki in clinical trials2013
Dr Pauline McCormack
Dr Simon Woods
Emma Heslop
Professor Volker Straub
Professor Katherine Bushby
et al.
Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational2013
Dr Simon Woods
Dr Pauline McCormack
Ethical issues in bio-marker research2011
Dr Pauline McCormack
Dr Simon Woods
Ethics at the edge of translation: the work of the TREAT-NMD Project Ethics Council2011
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