Functional Impairment of Hip Joint and Activities of Daily Living Failure in Patients with Multiple Hereditary Exostoses
Author:
Publisher
Springer Science and Business Media LLC
Subject
Orthopedics and Sports Medicine
Link
https://link.springer.com/content/pdf/10.1007/s43465-022-00681-w.pdf
Reference26 articles.
1. Akita, S., Murase, T., Yonenobu, K., Shimada, K., Masada, K., & Yoshikawa, H. (2007). Long-term results of surgery for forearm deformities in patients with multiple cartilaginous exostoses. Journal of Bone and Joint Surgery. American Volume, 89(9), 1993–1999.
2. Matsumoto, Y., Matsumoto, K., Harimaya, K., Okada, S., Doi, T., & Iwamoto, Y. (2015). Scoliosis in patients with multiple hereditary exostoses. European Spine Journal., 24(7), 1568–1573.
3. Matsumoto, K., Irie, F., Mackem, S., & Yamaguchi, Y. (2010). A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses. Proceedings of the National Academy of Sciences United States of America, 107(24), 10932–10937.
4. Ishimaru, D., Gotoh, M., Takayama, S., Kosaki, R., Matsumoto, Y., Narimatsu, H., Sato, T., Kimata, K., Akiyama, H., Shimizu, K., & Matsumoto, K. (2016). Large-scale mutational analysis in the EXT1 and EXT2 genes for Japanese patients with multiple osteochondromas. BMC Genetics, 9(17), 52.
5. Matsumoto, K., Ogawa, H., Nozawa, S., & Akiyama, H. (2020). An analysis of osteoporosis in patients with hereditary multiple exostoses. Osteoporosis International, 31(12), 2355–2361.
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