Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants

por Tang, Bei-Sha
Publicado 2016

Parkinson's Disease and Cognitive Impairment

por Yang, Yang, Tang, Bei-sha, Guo, Ji-feng
Publicado 2016

Research advances on neurite outgrowth inhibitor B receptor

por Zhang, Rui, Tang, Bei‐sha, Guo, Ji‐feng
Publicado 2020

The Progress of Induced Pluripotent Stem Cells as Models of Parkinson's Disease

por Kang, Ji-feng, Tang, Bei-sha, Guo, Ji-feng
Publicado 2016

PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

por Guo, Yu-pei, Tang, Bei-sha, Guo, Ji-feng
Publicado 2018

Telomere Length and COVID-19 Outcomes: A Two-Sample Bidirectional Mendelian Randomization Study

por Jiang, Li, Tang, Bei-sha, Guo, Ji-feng, Li, Jin-chen
Publicado 2022

Microglial Activation in the Pathogenesis of Huntington’s Disease

por Yang, Hui-Ming, Yang, Su, Huang, Shan-Shan, Tang, Bei-Sha, Guo, Ji-Feng
Publicado 2017

Can brain impermeable BACE1 inhibitors serve as anti-CAA medicine?

por Li, Jian-Ming, Huang, Li-Ling, Liu, Fei, Tang, Bei-Sha, Yan, Xiao-Xin
Publicado 2017

Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in China

por Liu, Lei, Li, Xiao-Bo, Hu, Zheng-Mao, Huang, Shun-Xiang, Tang, Bei-Sha, Zhang, Ru-Xu
Publicado 2020

VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation

por Tian, Yun, Tang, Fu-Lei, Sun, XiangDong, Wen, Lei, Mei, Lin, Tang, Bei-Sha, Xiong, Wen-Cheng
Publicado 2015

A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature

por Jiang, Hong, Shi, Yu-ting, Wang, Jun-ling, Tang, Bei-sha, Wang, Jun-yu, Peng, Ze-feng, Xiao, De-sheng
Publicado 2010

Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-Analysis

por Zhang, Yuan, Sun, Qi-ying, Zhao, Yu-wen, Shu, Li, Guo, Ji-feng, Xu, Qian, Yan, Xin-xiang, Tang, Bei-sha
Publicado 2015

Identification of Ser465 as a novel PINK1 autophosphorylation site

por Guo, Ji-feng, Yao, Ling-yan, Sun, Qi-ying, Cui, Yi-ting, Yang, Yang, Xu, Qian, Yan, Xin-xiang, Tang, Bei-sha
Publicado 2017

Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients

por Tang, Yan, Xiao, Xue, Xie, Hua, Wan, Chang-min, Meng, Li, Liu, Zhen-hua, Liao, Wei-hua, Tang, Bei-sha, Guo, Ji-feng
Publicado 2017

Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism

por Yang, Yang, Tang, Bei-sha, Weng, Ling, Li, Nan, Shen, Lu, Wang, Jian, Zuo, Chuan-tao, Yan, Xin-xiang, Xia, Kun, Guo, Ji-feng
Publicado 2015

Analysis of EIF4G1 in ethnic Chinese

por Li, Kai, Tang, Bei-sha, Guo, Ji-feng, Lou, Ming-xing, Lv, Zhan-yun, Liu, Zhen-hua, Tian, Yun, Song, Cheng-yuan, Xia, Kun, Yan, Xin-xiang
Publicado 2013

Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson’s disease in Chinese Han population

por Liao, Xin-xin, Zhan, Zi-xiong, Luo, Ying-ying, Li, Kai, Wang, Jun-ling, Guo, Ji-feng, Yan, Xin-xiang, Xia, Kun, Tang, Bei-sha, Shen, Lu
Publicado 2013

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

por Jiao, Bin, Guo, Ji-feng, Wang, Ya-qin, Yan, Xin-xiang, Zhou, Lin, Liu, Xiao-yan, Zhang, Fu-feng, Zhou, Ya-fang, Xia, Kun, Tang, Bei-sha, Shen, Lu
Publicado 2013

RAB39B gene mutations are not linked to familial Parkinson’s disease in China

por Kang, Ji-feng, Luo, Yang, Tang, Bei-sha, Wan, Chang-min, Yang, Yang, Li, Kai, Liu, Zhen-hua, Sun, Qi-ying, Xu, Qian, Yan, Xin-xiang, Guo, Ji-feng
Publicado 2016

Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth

por Zhao, Xin, Jiang, Ming-Ming, Yan, Yi-Zhou, Liu, Lei, Xie, Yong-Zhi, Li, Xiao-Bo, Hu, Zheng-Mao, Zi, Xiao-Hong, Xia, Kun, Tang, Bei-Sha, Zhang, Ru-Xu
Publicado 2018