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The International Journal of Neuroscience|May 9, 2012
Spinocerebellar ataxia type 28 (SCA28) is an uncommon cause of dominant ataxia among Chinese kindredsDandan Jia, Beisha Tang, Zhao Chen, et al.
Brain Communications|February 21, 2025
Glymphatic dysfunction exacerbates cognitive decline by triggering cortical degeneration in Parkinson's disease: evidence from diffusion-tensor MRIYang Zhao, Changyuan Xu, Yufan Chen, et al.
Neuroscience Letters|May 15, 2012
Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han populationZhao Chen, Xiaohui Li, Beisha Tang, et al.
Cerebellum (London, England)|April 15, 2015
High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease ProgressionYuting Shi, Chunrong Wang, Fengzhen Huang, et al.
Neurobiology of Aging|June 4, 2023
Mutation analysis of the ECE1 gene in late-onset Alzheimer's diseaseZhanfang Sun, Cheng Zhao, Xueming Liu, et al.
Neurobiology of Disease|August 31, 2025
Multimodal MRI biomarkers optimize differentiation between progressive supranuclear palsy and Parkinson's diseaseTong Chen, Tao Gong, Yufan Chen, et al.
Neurobiology of Aging|April 22, 2014
APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han populationHuirong Peng, Chunrong Wang, Zhao Chen, et al.
Scientific Reports|February 13, 2016
Prediction of orthostatic hypotension in multiple system atrophy and Parkinson diseaseZhanfang Sun, Dandan Jia, Yuting Shi, et al.
JCI Insight|February 28, 2020
Identification of Alzheimer's disease-associated rare coding variants in the ECE2 geneXinxin Liao, Fang Cai, Zhanfang Sun, et al.
Aging and Disease|May 10, 2023
Age and Sex Affect Essential Tremor (ET) Plus: Clinical Heterogeneity in ET Based on the National Survey in ChinaQiying Sun, Runcheng He, Hongyan Huang, et al.
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