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Nick Meade
Nick Meade
Genetic Alliance UK
Medical education
Nursing
Family medicine
Health care
Medicine
5
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8
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Rare Disease Healthcare Experience: Qualitative Survey and Workshop Findings in the Context of UK Policy Development
2021
Jennifer Jones
Amy Simpson
Nick Meade
Daphnee Pushparajah
David Newman
Amy Hunter
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Rare musculoskeletal diseases in adults: a research priority setting partnership with the James Lind Alliance.
2020
Orphanet Journal of Rare Diseases
Gerda Mickute
Kristina Staley
Heather DeLaney
Oliver Gardiner
Amy Hunter
Richard Keen
Lorraine Lockhart
Nick Meade
Maria Newman
Stuart H. Ralston
Elaine Rush
Sheela Upadhyaya
Sandra Regan
Laura Watts
Jennifer Walsh
Paul White
Roger M. Francis
M Kassim Javaid
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Rare diseases and mental health in the UK - a quantitative survey and multi-stakeholder workshop
2019
Rosa Spencer-Tansley
Nick Meade
Farhana Ali
Amy Simpson
Amy Hunter
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"in the Patients' Hands"- a Structured Survey of Patient Voices to Prioritise Research Questions in Rare Inherited Anaemias: The James Lind Alliance Priority Setting Partnership
2018
Blood
Jenny Welch
Nick Meade
Dominic Messenger
Amy Hunter
Anupama Rao
Subarna Chakravorty
Rachel Wearmouth
Anju Chalin
Kristina Staley
Sheela Upadhyaya
I. Roberts
N Roy
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Strengthening international patient advocacy perspectives on patient involvement in HTA within the HTAi Patient and Citizen Involvement Interest Group – Commentary
2017
Research Involvement and Engagement
Janet L. Wale
Anna Mae Scott
Neil Bertelsen
Nick Meade
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Citations (6)
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