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Journal of the Neurological Sciences|October 13, 2012
Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese populationYongping Chen, Ke Chen, Jean-Marc Burgunder, et al.
Neuroimage. Clinical|August 3, 2017
Altered praxis network underlying limb kinetic apraxia in Parkinson's disease - an fMRI studyStefanie Kübel, Katharina Stegmayer, Tim Vanbellingen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 27, 2011
Association of GWAS loci with PD in ChinaXue-Li Chang, Xue-Ye Mao, Hui-Hua Li, et al.
Frontiers in Neurology|December 6, 2021
Evaluation of Blood Glial Fibrillary Acidic Protein as a Potential Marker in Huntington's DiseaseHuajing You, Tengteng Wu, Gang Du, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 25, 2011
Deep brain stimulation of the globus pallidus internal improves symptoms of chorea-acanthocytosisPeng Li, Rui Huang, Wei Song, et al.
Journal of the Neurological Sciences|December 24, 2010
Functional parkin promoter polymorphism in Parkinson's disease: new data and meta-analysisXue-Li Chang, Xue-Ye Mao, Hui-Hua Li, et al.
Journal of Huntington'S Disease|September 19, 2022
The Chinese Version of UHDRS in Huntington's Disease: Reliability and Validity AssessmentXiao-Yan Li, Yu-Feng Bao, Juan-Juan Xie, et al.
Journal of Neuroscience Research|December 31, 2005
Reorganization of CA3 area of the mouse hippocampus after pilocarpine induced temporal lobe epilepsy with special reference to the CA3-septum pathwayDong Liang Ma, Yong Cheng Tang, Peng Min Chen, et al.
Muscle & Nerve|April 30, 2004
Exon 17 skipping in CLCN1 leads to recessive myotonia congenitaLie Chen, Martin Schaerer, Zen H Lu, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 4, 2008
Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutationYee-Cheun Chan, Jean-Marc Burgunder, Einar Wilder-Smith, et al.
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