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Neuroscience Letters|March 8, 2022
Rare missense variants in the PPP2R5D gene associated with Parkinson's disease in the Han Chinese populationPingping Ning, Kelu Li, Hui Ren, et al.
Neuroscience Letters|May 19, 2019
Alpha-synuclein gene polymorphism affects risk of dementia in Han Chinese with Parkinson's diseaseJinhua Zheng, Qiuling Zang, Fengyun Hu, 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.
Psychiatry Investigation|October 26, 2020
The Gene Polymorphism of VMAT2 Is Associated with Risk of Schizophrenia in Male Han ChineseHongying Han, Xiaowei Xia, Huirong Zheng, 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.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 24, 2015
Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese populationXinglong Yang, Jing Xi, Ran An, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 5, 2024
Phenotypic and mutational spectrum of 17 Chinese patients with Menkes DiseaseFang Xu, Hongyan Huang, Qiuyan Shen, et al.
Japanese Journal of Infectious Diseases|May 1, 2020
Acute Flaccid Paralysis as the Initial Manifestation of Japanese Encephalitis: a Case ReportQiuyan Shen, Yan Li, Haitao Lu, et al.
Parkinsonism & Related Disorders|June 9, 2016
Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literatureXinglong Yang, Quanzhen Zhao, Ran An, et al.
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