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Year Number of Results
2015 1
2016 3
2017 1
2021 1
2022 0
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Page 1
Short report: craniosynostosis, a late complication of nutritional rickets.
Forestier-Zhang LY, Arundel P, Gilbey-Cross R, Mughal MZ, Offiah AC, Cheung MS. Forestier-Zhang LY, et al. J Pediatr Endocrinol Metab. 2021 Apr 16;34(8):1055-1060. doi: 10.1515/jpem-2020-0580. Print 2021 Aug 26. J Pediatr Endocrinol Metab. 2021. PMID: 33866705 Free 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: forestier zhang 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.
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: forestier zhang 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.