Author:
Akiyama Masaharu,Yamaoka Masayoshi,Mikami-Terao Yoko,Ohyama Wataru,Yokoi Kentaro,Arakawa Yasuhiro,Takita Junko,Suzuki Hideaki,Yamada Hisashi
Funder
The Jikei University Research Fund
Publisher
Springer Science and Business Media LLC
Reference16 articles.
1. Verdegaal SHM, Bovee JVMG, Pansuriya TC, Grimer RJ, Ozger H, Jutte PC, et al. Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patients. Oncologist. 2011;16:1771–9.
2. Amary MF, Damato S, Halai D, Eskandarpour M, Berisha F, Bonar F, et al. Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2. Nature Genet. 2011;43:1262–6.
3. Pansuriya TC, van Eijk R, d’Adamo P, van Ruler MAJH, Kuijjer ML, Oosting J, et al. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nature Genet. 2011;43:1256–61.
4. Rector JT, Gray CL, Sharpe RW, Hall FW, Thomas W, Jones W. Acute lymphoid leukemia associated with Maffucci’s syndrome. Am J Pediatr Hematol Oncol. 1993;15:427–9.
5. Au WY, Ooi GC, Ma SK, Wan TSK, Kwong YL. Chronic myeloid leukemia in an adolescent Ollier’s disease after intensive X-ray exposure. Leuk Lymphoma. 2004;45:613–6.
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献