Wei Luo

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 23

Top Topics

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Tremor and other hyperkinetic movements (New York, N.Y.)

This page only lists publications with an associated author ORCID identifier.

Publications

Ping Wang, Xinhui Chen, Miao Chen, Leilei Gao, Bing Xiong, Changmeng Ji, Qian Shen, Yuanqing Shen, Sheng Wu, Yanhong Pan, Jinhui Li, Bo Wang, Wei Luo
Dysphagia Pattern in Early to Moderate Parkinson's Disease Caused by Abnormal Pharyngeal Kinematic Function. Dysphagia (2024)
Weili Luo, Xiaosheng Zheng, Zhiru Lin, Wei Luo
Careful Phenotypic Characterization of Tremor Phenomenology in a Patient with Spinocerebellar Ataxia Type 12-Tremor Features Do Not Match Those of Essential Tremor. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Fan Zhang, Peng Liu, Jiaxiang Li, Zhidong Cen, Wei Luo
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2024)
Weili Luo, Xiaosheng Zheng, Zhiru Lin, Wei Luo
Careful Phenotypic Characterization of Tremor Phenomenology in a Patient with Spinocerebellar Ataxia Type 12-Tremor Features Do Not Match Those of Essential Tremor. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Fan Zhang, Peng Liu, Jiaxiang Li, Zhidong Cen, Wei Luo
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 45 (4) (2024)
Fan Zhang, Peng Liu, Jiaxiang Li, Zhidong Cen, Wei Luo
A novel ATP13A2 variant causing complicated hereditary spastic paraplegia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 45 (4) (2024)
Xinhui Chen, Yihua Shi, Feng Fu, Lebo Wang, Hongying Yu, Dehao Yang, Xinchen Wang, Chenxin Ying, Haoyu Wang, Zhiru Lin, Haotian Wang, Fan Zhang, Xiaosheng Zheng, Yuru Guo, Yaoting Wang, YiHeng Zeng, Miao Zhao, Yiling Chen, Jiaxiang Li, Haibin Xia, Jiawen Chen, Bo Wang, Sheng Wu, Fei Xie, Jianhua Feng, Zhidong Cen, Wei Luo
A Homozygous Variant in NAA60 Is Associated with Primary Familial Brain Calcification. Movement disorders : official journal of the Movement Disorder Society (2024)
Xinhui Chen, Fan Zhang, Yihua Shi, Haotian Wang, Miao Chen, Dehao Yang, Lebo Wang, Peng Liu, Fei Xie, Jiawen Chen, Aisi Fu, Ben Hu, Bo Wang, Zhiyuan Ouyang, Sheng Wu, Zhiru Lin, Zhidong Cen, Wei Luo
Origin and evolution of pentanucleotide repeat expansions at the familial cortical myoclonic tremor with epilepsy type1 - SAMD12 locus. European journal of human genetics : EJHG (2024)
Xinhui Chen, Fan Zhang, Yihua Shi, Haotian Wang, Miao Chen, Dehao Yang, Lebo Wang, Peng Liu, Fei Xie, Jiawen Chen, Aisi Fu, Ben Hu, Bo Wang, Zhiyuan Ouyang, Sheng Wu, Zhiru Lin, Zhidong Cen, Wei Luo
Origin and evolution of pentanucleotide repeat expansions at the familial cortical myoclonic tremor with epilepsy type1 - SAMD12 locus. European journal of human genetics : EJHG (2024)
Zhiru Lin, Jiaxiang Li, Wei Luo
A DLB patient with complicated CAA interruptions and intermediate alleles of 43 CAG/CAA repeats in TBP. Acta neurologica Belgica (2023)
Xinhui Chen, Zhidong Cen, Bo Wang, Peng Liu, Wei Luo
Multiple System Atrophy-like Phenotype Accompanied by Prominent Weight Loss and Fatigue. Movement disorders clinical practice 10 (Suppl 3) (2023)
Yao Ding, Zhidong Cen, Yang Zheng, Xia Qiu, Yumao Ye, Xinhui Chen, Lingli Hu, Bo Wang, Zhongjin Wang, Houmin Yin, Chunhong Shen, Wenjie Ming, Yi Ge, Fei Xie, Dehao Yang, Zhiyuan Ouyang, Haotian Wang, Sheng Wu, Mei-Ping Ding, Shuang Wang, Wei Luo
Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 1. Annals of clinical and translational neurology (2023)
Jiaxiang Li, Zhiru Lin, Nan Jin, Xiaosheng Zheng, Wei Luo
Isolated Head Tremor as an Initial Presentation of Ataxia with Vitamin E Deficiency: A Case Report. Movement disorders clinical practice 10 (11) (2023)
Peng Liu, Dehao Yang, Fan Zhang, Shuqi Chen, Fei Xie, Yong Luo, Haotian Wang, Yueting Chen, Zhiru Lin, Lebo Wang, Xinhui Chen, Bo Wang, Sheng Wu, Zhiyuan Ouyang, Zhidong Cen, Wei Luo
The role of NOTCH2NLC in Parkinson's disease: A clinical, neuroimaging, and pathological study. European journal of neurology 29 (6) (2022)
Bo Wang, Haotian Wang, Zhidong Cen, Jiachen Yuan, Dehao Yang, Xinhui Chen, Fei Xie, Lebo Wang, Sheng Wu, Zhiyuan Ouyang, Yu-Feng Zang, Wei Luo
White matter alterations in familial cortical myoclonic tremor with epilepsy type 1. Epilepsia 63 (5) (2022)
Fei Xie, Shuqi Chen, Peng Liu, Xinhui Chen, Wei Luo
SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia. Journal of human genetics (2021)
Yueting Chen, Peng Liu, Fei Xie, Bo Wang, Zhiru Lin, Wei Luo
A heterozygous de novo PSEN1 mutation in a patient with early-onset parkinsonism. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2021)
Ping Wang, Bo Wang, Xinhui Chen, Bing Xiong, Fangyao Xie, Sheng Wu, Yinshan Tang, Shuqi Chen, Xueping Ding, Peng Liu, Wei Luo
Six-Year Follow-Up of Dysphagia in Patients with Parkinson's Disease. Dysphagia (2021)
Bo Wang, Jue Wang, Zhidong Cen, Wei Wei, Fei Xie, You Chen, Haiyang Sun, Yunsong Hu, Dehao Yang, Yuting Lou, Xinhui Chen, Zhiyuan Ouyang, Si Chen, Haotian Wang, Lebo Wang, Shuang Wang, Xia Qiu, Yao Ding, Houmin Yin, Sheng Wu, Baorong Zhang, Yu-Feng Zang, Wei Luo
Altered Cerebello-Motor Network in Familial Cortical Myoclonic Tremor With Epilepsy Type 1. Movement disorders : official journal of the Movement Disorder Society 35 (6) (2020)
You Chen, Zhidong Cen, Xinhui Chen, Haotian Wang, Si Chen, Dehao Yang, Feng Fu, Lebo Wang, Peng Liu, Hongwei Wu, Xiaosheng Zheng, Fei Xie, Zhiyuan Ouyang, Yun Zhang, Yongji Zhou, Xuerong Huang, Feng Wang, Guangsu Huang, Hongwei An, Yubing Liang, Weijun Hong, Anli Wang, Shuangling Huang, Wenhai Chen, Lili Yin, Yan Yang, Huayun Huang, Ruxin Zeng, Na Zhao, Biao Jiang, Baorong Zhang, Wei Luo, null null
MYORG Mutation Heterozygosity Is Associated With Brain Calcification. Movement disorders : official journal of the Movement Disorder Society 35 (4) (2020)
Zhidong Cen, You Chen, Dehao Yang, Qingchen Zhu, Si Chen, Xinhui Chen, Bo Wang, Fei Xie, Zhiyuan Ouyang, Zhengwen Jiang, Aisi Fu, Ben Hu, Houmin Yin, Xia Qiu, Feng Yu, Xiaoping Du, Weicheng Hao, Yuxi Liu, Haotian Wang, Lebo Wang, Xiafei Yu, Yichuan Xiao, Chunyu Liu, Jianfeng Xiao, Yongxing Zhou, Wei Yang, Baorong Zhang, Wei Luo
Intronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy. Movement disorders : official journal of the Movement Disorder Society 34 (10) (2019)
You Chen, Zhidong Cen, Xiaosheng Zheng, Qinqing Pan, Xinhui Chen, Lili Zhu, Si Chen, Hongwei Wu, Fei Xie, Haotian Wang, Dehao Yang, Lebo Wang, Baorong Zhang, Wei Luo
LRP10 in autosomal-dominant Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 34 (6) (2019)
You Chen, Feng Fu, Si Chen, Zhidong Cen, Haiyan Tang, Jinxiu Huang, Fei Xie, Xiaosheng Zheng, Dehao Yang, Haotian Wang, Xuerong Huang, Yun Zhang, Yongji Zhou, Jing-Yu Liu, Wei Luo
Evaluation of MYORG mutations as a novel cause of primary familial brain calcification. Movement disorders : official journal of the Movement Disorder Society 34 (2) (2018)