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Nature Genetics|March 18, 1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseA Sakuntabhai, V Ruiz-Perez, S Carter, et al.
Health Technology Assessment (Winchester, England)|May 3, 2019
Treatment of first-time traumatic anterior shoulder dislocation: the UK TASH-D cohort studyJonathan L Rees, Anjali Shah, Katherine Edwards, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|September 29, 2025
General practitioner workforce sustainability to maximise effective and equitable patient care: a realist reviewEmily Owen-Boukra, Bryan Burford, Tanya Cohen, et al.
Frontiers in Physiology|June 12, 2013
Inflammatory markers associated with osteoarthritis after destabilization surgery in young mice with and without Receptor for Advanced Glycation End-products (RAGE)D Justin Larkin, Jeffrey Z Kartchner, Alexander S Doxey, et al.
Plos Medicine|September 21, 2020
TIDieR-Placebo: A guide and checklist for reporting placebo and sham controlsJeremy Howick, Rebecca K Webster, Jonathan L Rees, et al.
Pilot and Feasibility Studies|August 21, 2021
Findings from the patch augmented rotator cuff surgery (PARCS) feasibility studyJonathan A Cook, Mathew Baldwin, Cushla Cooper, et al.
Lancet (London, England)|November 25, 2017
Arthroscopic subacromial decompression for subacromial shoulder pain (CSAW): a multicentre, pragmatic, parallel group, placebo-controlled, three-group, randomised surgical trialDavid J Beard, Jonathan L Rees, Jonathan A Cook, et al.
The New England Journal of Medicine|March 5, 2005
U.K. Controlled trial of intrapleural streptokinase for pleural infectionNicholas A Maskell, Christopher W H Davies, Andrew J Nunn, et al.
Health Technology Assessment (Winchester, England)|March 1, 2021
Patch augmentation surgery for rotator cuff repair: the PARCS mixed-methods feasibility studyJonathan A Cook, Mathew Baldwin, Cushla Cooper, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
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