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Neuropathic-like Pain in Fibrous Dysplasia/McCune-Albright Syndrome.
Spencer TL, Watts L, Soni A, Pinedo-Villanueva R, Heegaard AM, Boyce AM, Javaid MK. Spencer TL, et al. Among authors: watts l. J Clin Endocrinol Metab. 2022 May 17;107(6):e2258-e2266. doi: 10.1210/clinem/dgac120. J Clin Endocrinol Metab. 2022. PMID: 35262711 Free PMC article.
Improving patient outcomes in fibrous dysplasia/McCune-Albright syndrome: an international multidisciplinary workshop to inform an international partnership.
Boyce AM, Turner A, Watts L, Forestier-Zhang L, Underhill A, Pinedo-Villanueva R, Monsell F, Tessaris D, Burren C, Masi L, Hamdy N, Brandi ML, Chapurlat R, Collins MT, Javaid MK. Boyce AM, et al. Among authors: watts l. Arch Osteoporos. 2017 Dec;12(1):21. doi: 10.1007/s11657-016-0271-6. Epub 2017 Feb 27. Arch Osteoporos. 2017. PMID: 28243882 Free PMC article.
Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.
Forestier-Zhang L, Watts L, Turner A, Teare H, Kaye J, Barrett J, Cooper C, Eastell R, Wordsworth P, Javaid MK, Pinedo-Villanueva R. Forestier-Zhang L, et al. Among authors: watts l. Orphanet J Rare Dis. 2016 Nov 28;11(1):160. doi: 10.1186/s13023-016-0538-4. Orphanet J Rare Dis. 2016. PMID: 27894323 Free PMC article.
The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.
Javaid MK, Forestier-Zhang L, Watts L, Turner A, Ponte C, Teare H, Gray D, Gray N, Popert R, Hogg J, Barrett J, Pinedo-Villanueva R, Cooper C, Eastell R, Bishop N, Luqmani R, Wordsworth P, Kaye J. Javaid MK, et al. Among authors: watts l. Orphanet J Rare Dis. 2016 Nov 8;11(1):150. doi: 10.1186/s13023-016-0528-6. Orphanet J Rare Dis. 2016. PMID: 27825362 Free PMC article.
The RUDY study: using digital technologies to enable a research partnership.
Teare HJA, Hogg J, Kaye J, Luqmani R, Rush E, Turner A, Watts L, Williams M, Javaid MK. Teare HJA, et al. Among authors: watts l. Eur J Hum Genet. 2017 Jun;25(7):816-822. doi: 10.1038/ejhg.2017.57. Epub 2017 Apr 26. Eur J Hum Genet. 2017. PMID: 28443622 Free PMC article.
Rare musculoskeletal diseases in adults: a research priority setting partnership with the James Lind Alliance.
Mickute G, Staley K, Delaney H, Gardiner O, Hunter A, Keen R, Lockhart L, Meade N, Newman M, Ralston S, Rush E, Upadhyaya S, Regan S, Watts L, Walsh J, White P, Francis RM, Javaid MK. Mickute G, et al. Among authors: watts l. Orphanet J Rare Dis. 2020 May 19;15(1):117. doi: 10.1186/s13023-020-01398-5. Orphanet J Rare Dis. 2020. PMID: 32430048 Free PMC article.
277 results