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International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia.
Savarirayan R, Ireland P, Irving M, Thompson D, Alves I, Baratela WAR, Betts J, Bober MB, Boero S, Briddell J, Campbell J, Campeau PM, Carl-Innig P, Cheung MS, Cobourne M, Cormier-Daire V, Deladure-Molla M, Del Pino M, Elphick H, Fano V, Fauroux B, Gibbins J, Groves ML, Hagenäs L, Hannon T, Hoover-Fong J, Kaisermann M, Leiva-Gea A, Llerena J, Mackenzie W, Martin K, Mazzoleni F, McDonnell S, Meazzini MC, Milerad J, Mohnike K, Mortier GR, Offiah A, Ozono K, Phillips JA 3rd, Powell S, Prasad Y, Raggio C, Rosselli P, Rossiter J, Selicorni A, Sessa M, Theroux M, Thomas M, Trespedi L, Tunkel D, Wallis C, Wright M, Yasui N, Fredwall SO. Savarirayan R, et al. Among authors: cheung ms. Nat Rev Endocrinol. 2022 Mar;18(3):173-189. doi: 10.1038/s41574-021-00595-x. Epub 2021 Nov 26. Nat Rev Endocrinol. 2022. PMID: 34837063 Free article. Review.
Achondroplasia Foramen Magnum Score: screening infants for stenosis.
Cheung MS, Irving M, Cocca A, Santos R, Shaunak M, Dougherty H, Siddiqui A, Gringras P, Thompson D. Cheung MS, et al. Arch Dis Child. 2021 Feb;106(2):180-184. doi: 10.1136/archdischild-2020-319625. Epub 2020 Sep 3. Arch Dis Child. 2021. PMID: 32883660
Lifetime impact of achondroplasia: Current evidence and perspectives on the natural history.
Hoover-Fong J, Cheung MS, Fano V, Hagenas L, Hecht JT, Ireland P, Irving M, Mohnike K, Offiah AC, Okenfuss E, Ozono K, Raggio C, Tofts L, Kelly D, Shediac R, Pan W, Savarirayan R. Hoover-Fong J, et al. Among authors: cheung ms. Bone. 2021 May;146:115872. doi: 10.1016/j.bone.2021.115872. Epub 2021 Feb 3. Bone. 2021. PMID: 33545406 Free article. Review.
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. Among authors: cheung ms. 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.
Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era.
Sabir AH, Morley E, Sheikh J, Calder AD, Beleza-Meireles A, Cheung MS, Cocca A, Jansson M, Lillis S, Patel Y, Yau S, Hall CM, Offiah AC, Irving M. Sabir AH, et al. Among authors: cheung ms. BMC Med Genomics. 2021 Jun 6;14(1):148. doi: 10.1186/s12920-021-00993-0. BMC Med Genomics. 2021. PMID: 34092239 Free PMC article.
163 results