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Multiple Sclerosis and Related Disorders|June 25, 2019
Association between suicide and multiple sclerosis: An updated meta-analysisQiuyan Shen, Haitao Lu, Dan Xie, et al.
Genetic Testing and Molecular Biomarkers|September 10, 2016
SNP rs1805874 of the Calbindin1 Gene Is Associated with Parkinson's Disease in Han ChineseXinglong Yang, Quanzhen Zhao, Ran An, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|August 28, 2015
Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han ChineseXinglong Yang, Quanzhen Zhao, Ran An, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 23, 2015
Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literatureQuanZhen Zhao, Xinglong Yang, SiJia Tian, et al.
Parkinson'S Disease|March 31, 2017
Festination Correlates with SNCA Polymorphism in Chinese Patients with Parkinson's DiseaseJinhua Zheng, Xinglong Yang, Quanzhen Zhao, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 13, 2017
Onset of bladder and motor symptoms in multiple system atrophy: differences according to phenotypeJinhua Zheng, Xinglong Yang, Yalan Chen, et al.
Journal of the Neurological Sciences|January 30, 2017
HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohortXinglong Yang, JinHua Zheng, Sijia Tian, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|March 14, 2019
Frequency and factors related to drooling in Chinese patients with multiple system atrophy: a cross-sectional studyYalan Chen, Hongyan Huang, Pingping Ning, et al.
Parkinson'S Disease|August 7, 2015
Polymorphism in the Vesicular Monoamine Transporter 2 Gene Decreases the Risk of Parkinson's Disease in Han Chinese MenXinglong Yang, Pingrong Xu, Quanzhen Zhao, et al.
Journal of the Neurological Sciences|August 20, 2016
Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosisXinglong Yang, Ran An, Quanzhen Zhao, et al.
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