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Neural Regeneration Research|August 12, 2021
Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control studyYa-Fei Wen, Xue-Wen Xiao, Lu Zhou, et al.The Clinical Respiratory Journal|August 12, 2015
Multinodule abnormalities of the tracheobronchus: bronchoscopy findings and clinical diagnosisJian An, Hua-Ping Yang, Cheng-Ping Hu, et al.Frontiers in Aging Neuroscience|August 15, 2022
Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer's diseaseMei-Dan Wan, Hui Liu, Xi-Xi Liu, et al.Journal of the Neurological Sciences|October 7, 2008
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosumShu-sheng Liao, Lu Shen, Juan Du, et al.Brain : a Journal of Neurology|November 26, 2010
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencingJun Ling Wang, Xu Yang, Kun Xia, et al.Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 4, 2022
The Protective Effects of Osteocyte-Derived Extracellular Vesicles Against Alzheimer's Disease Diminished with AgingYa-Ling Jiang, Zhen-Xing Wang, Xi-Xi Liu, et al.American Journal of Human Genetics|June 11, 2019
Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related DisordersYun Tian, Jun-Ling Wang, Wen Huang, et al.Pageof 2