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Cerebellum (London, England)|July 2, 2013
Lithium chloride alleviates neurodegeneration partly by inhibiting activity of GSK3β in a SCA3 Drosophila modelDan-Dan Jia, Li Zhang, Zhao Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 3, 2006
[Lecithin-cholesterol acyltransferase gene 608C/T polymorphism associated with atherosclerotic cerebral infarction]Xiao-yan Zhu, Hong-wei Xu, Rong-yao Hou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 11, 2006
[Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L]Ru-xu Zhang, Bei-sha Tang, Xiao-hong Zi, et al.
Neurology India|July 18, 2013
Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland ChinaWen-Juan Guan, Xin-Jian Liu, Bei-Sha Tang, et al.
Frontiers in Neuroanatomy|November 23, 2017
Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's PatientsYan Tang, Xue Xiao, Hua Xie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2010
Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese populationQi-Ying Sun, Ji-Feng Guo, Lei Wang, et al.
Zhonghua Yi Xue Za Zhi|October 24, 2006
[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families]Xing-Wang Song, Bei-sha Tang, Hong Jiang, et al.
Journal of Neurology|February 11, 2010
Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonismJi-feng Guo, Xue-wei Zhang, Li-luo Nie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 13, 2006
[Study on aggregate formation mechanism of HSPB8 gene mutation resulting in CMT2L]Ru-xu Zhang, Bei-sha Tang, Xiao-hong Zi, et al.
Zhonghua Yi Xue Za Zhi|March 3, 2010
[Mutation analysis of MFN2 gene in Chinese patients with Charcot-Marie-Tooth disease]Ru-xu Zhang, Min Fu, Xiao-hong Zi, et al.
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