Items where authors include "Ozono, K."

Article

Kishnani, P.S. orcid.org/0000-0001-8251-909X, Rehder, C., Ozono, K. et al. (6 more authors) (2025) Revisiting the genetics of hypophosphatasia. Journal of Inherited Metabolic Disease, 48 (6). e70083. ISSN 0141-8955

Hoover-Fong, J., Cheung, M.S., Fano, V. et al. (14 more authors) (2021) Lifetime impact of achondroplasia: current evidence and perspectives on the natural history. Bone, 146. 115872. ISSN 8756-3282

Kishnani, P.S., Rush, E.T., Arundel, P. et al. (10 more authors) (2017) Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa. Molecular Genetics and Metabolism, 122 (1-2). pp. 4-17. ISSN 1096-7192

Bishop, N. orcid.org/0000-0001-7263-8546, Munns, C.F. and Ozono, K. (2016) Transformative therapy in hypophosphatasia. Archives of Disease in Childhood, 101 (6). ISSN 0003-9888