Pauline Mccormack

Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 13 publications

From embodiment to evidence: The harmful intersection of poor regulation of medical implants and obstructed narratives in embodied experiences of failed metal-on-metal hips.

From embodiment to evidence: The harmful intersection of poor regulation of medical implants and obstructed narratives in embodied experiences of failed metal-on-metal hips.

Journal: Health (London, England : 1997)

Published: June 05, 2023

Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis.

Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 26, 2019

Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesis.

Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: February 06, 2019

New Recommendation on Biological Materials Could Hamper Muscular Dystrophy Research.

New Recommendation on Biological Materials Could Hamper Muscular Dystrophy Research.

Journal: PLoS currents

Published: January 31, 2017

International Charter of principles for sharing bio-specimens and data.

International Charter of principles for sharing bio-specimens and data.

Journal: European journal of human genetics : EJHG

Published: June 17, 2016

'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research.

'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research.

Journal: European journal of human genetics : EJHG

Published: November 19, 2015

Improving the informed consent process in international collaborative rare disease research: effective consent for effective research.

Improving the informed consent process in international collaborative rare disease research: effective consent for effective research.

Journal: European journal of human genetics : EJHG

Published: August 07, 2015

International Charter of principles for sharing bio-specimens and data.

International Charter of principles for sharing bio-specimens and data.

Journal: European journal of human genetics : EJHG

Published: June 13, 2014

Precaution, governance and the failure of medical implants: the ASR((TM)) hip in the UK.

Precaution, governance and the failure of medical implants: the ASR((TM)) hip in the UK.

Journal: Life sciences, society and policy

Published: February 27, 2014

Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational.

Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational.

Journal: PLoS currents

Published: January 19, 2013

The therapeutic misconception, decision making and informed consent: the ethics of trial participation for neuromuscular disorders.

The therapeutic misconception, decision making and informed consent: the ethics of trial participation for neuromuscular disorders.

Journal: Neuromuscular disorders : NMD

Published: March 08, 2012

Therapeutic misconception: hope, trust and misconception in paediatric research.

Therapeutic misconception: hope, trust and misconception in paediatric research.

Journal: Health care analysis : HCA : journal of health philosophy and policy

Published: February 22, 2012

Showing 1-12 of 13

Last Updated: 09/26/2026