Browsing publications by Dr Pauline McCormack

Newcastle AuthorsTitleYearFull text
Dr Simon Woods
Dr Pauline McCormack
Professor Hanns Lochmuller
Professor Volker Straub
Improving the informed consent process in international collaborative rare disease research: Effective consent for effective research2016
Dr Pauline McCormack
Dr Simon Woods
Professor Hanns Lochmuller
Professor Mats Hansson
International Charter of principles for sharing bio-specimens and data (vol 23, pg 721, 2015)2016
Dr Pauline McCormack
Rare Disease, Big Data: the views of rare disease patients on systems for sharing data and biospecimens2016
Dr Pauline McCormack
Professor Hanns Lochmuller
'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research2016
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 data2015
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
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