[5] Zhang ShuShan, Fang DengFu, Burgunder Jean-Marc, Chen XuePing, Zhang YangWei, Shang HuiFang. Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China. European J Neurology. 2010, 17: 846-851. (Corresponding author)
[6] Chen XuePing, Hu XiaoHui, Wu ShuHui, Zhang YangWei, Xiao Bo, Shang HuiFang. RNA Interference-Mediated Inhibition of Wild-Type Torsin A Expression Increases Apoptosis Caused by Oxidative Stress in Cultured Cells. Neurochemical Research. 2010, 35: 1214-1223. (Corresponding author)
[7] Guo XiaoYan, Zhang Shushan, Burgunder Jean-Marc, Shang HuiFang. Clinical features of Huntington disease in 243 Chinese patients. NEURAL REGENERATION RESEARCH. 2010,5(2):102-107. (Corresponding author)
[8] Fang DF, Zhang SS, Guo XY, Zeng Y, Yang Y, Zhou D, Shang HF. Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west www.med126.com China. Amyotroph Lateral Scler. 2009, 10(1):1-6. (Corresponding author).
[9] Xueping Chen, Huifang Shang, Zuming Luo. Genetic classification and molecular mechanisms of primary dystonia. Neural Regen Res, 2008, 3(3), 296-300. (Corresponding author).
[10] Yangwei Zhang, Shushan Zhang, Huifang Shang. Clinical characteristics of myotonia congenita in China: Literature analysis of the past 30 years. Neural Regen Res, 2008, 3(2), 216-20. (Corresponding author).
[11] Qin Chen, Su Lui, Jian-Gang Wang, Luo Ou-Yang, Dong Zhou, Jean-Marc Burgunder, Qi-Yong Gong, Hui-Fang Shang. Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum. Neuroscience Letters, 441(1): 21-24.(corresponding author)
[12] Xue-Ping Chen, Yang-Wei Zhang, Shu-Shan Zhang, Qin Chen, Jean-Marc Burgunder, Shu-Hui Wu, Yuan Yang, Zu-Ming Luo, Hui-Fang Shang. A novel mutation of epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome. Movement Disorders，2008,23(10): 1472-1475. (corresponding author)
[13] Qin Chen, Xue-Ping Chen, Ling Zou, Dong Zhou, Qi-Yong Gong, Jean-Marc Burgunder, Hui-Fang Shang. High brain iron level in www.med126.com asymptomatic carriers of heterozygous ceruloplasmin gene mutations. Movement Disorders, 2008, 23(6):916-917). (Corresponding author)
[14] Shu-Shan Zhang, Qin Chen, Xue-Ping Chen, Jian-Gang Wang, Jean-Marc Burgunder, Yuan Yang, Hui-Fang Shang. Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum. Movement Disorders, 2008,23(6):918-919.(Corresponding author)
[15] H. Shang, D. Lang, J.-M. Burgunder and A. Kaelin-Lang. Screening of GABAA-receptor gene mutations in primary dystonia. Eur J Neurol. 2007, 14(10):1179-81.
[16] HuiFang Shang, XiaoFeng Jiang, Jean-Marc Burgunder, Qin Chen, Dong Zhou. Novel mutation of ceruloplasmin gene causing cognitive and movement disorder with Diabetic mellitus. Movement Disorders, 2006, 21(12):2217-2220. (Corresponding author)
联系方式:
电话： 028-85423038 　　　邮箱:hfshang@yahoo.com

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