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Chen, Qin; Lui, Su; Wang, Jian-Gang; Ou-Yang, Luo; Zhou, Dong; Burgunder, Jean-Marc; Gong, Qi-Yong; Shang, Hui-Fang (2008). Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum. Neuroscience letters, 441(1), pp. 21-4. Amsterdam: Elsevier 10.1016/j.neulet.2008.05.114
Chen, Xue-Ping; Zhang, Yang-Wei; Zhang, Shu-Shan; Chen, Qin; Burgunder, Jean-Marc; Wu, Shu-Hui; Yang, Yuan; Luo, Zu-Ming; Shang, Hui-Fang (2008). A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome. Movement disorders, 23(10), pp. 1472-5. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.22008
Chen, Qin; Chen, Xue-Ping; Zou, Ling; Zhou, Dong; Gong, Qi-Yong; Burgunder, Jean-Marc; Shang, Hui-Fang (2008). High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations. Movement disorders, 23(6), pp. 916-7. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21980
Zhang, Shu-Shan; Chen, Qin; Chen, Xue-Ping; Wang, Jian-Gang; Burgunder, Jean-Marc; Shang, Hui-Fang (2008). Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum. Movement disorders, 23(6), pp. 917-9. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21942
Shang, Hui-Fang; Jiang, Xiao-Feng; Burgunder, Jean-Marc; Chen, Qin; Zhou, Dong (2006). Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus. Movement disorders, 21(12), pp. 2217-20. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21121
