Hongwei Wu - Dept Neurol, Lishui Peoples Hosp

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MYORG Mutation Heterozygosity is Associated with Brain Calcification

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

Movement Disorders（2020）

引用13浏览0WOS引用

LRP10 in Autosomal-Dominant Parkinson's Disease

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

Movement disorders（2019）

引用20浏览0WOS引用

Biallelic Loss-of-function Mutations in JAM2 Cause Primary Familial Brain Calcification

Zhidong Cen,You Chen,Si Chen,Hong Wang,Dehao Yang, Hongmei Zhang,Hongwei Wu,Lebo Wang,Siyang Tang, Jia Ye, Jian Shen,Haotian Wang,Feng Fu,Xinhui Chen, Fei Xie,Peng Liu,Xuan Xu, Jianzhi Cao, Pan Cai,Qinqing Pan, Jieying Li,Wei Yang,Peng-Fei Shan,Yuezhou Li,Jing-Yu Liu,Baorong Zhang,Wei Luo

Brain（2019）

引用53浏览0WOS引用

Underestimated Disease Prevalence and Severe Phenotypes in Patients with Biallelic Variants: A Cohort Study of Primary Familial Brain Calcification from China

Si Chen,Zhidong Cen,Feng Fu,You Chen,Xinhui Chen,Dehao Yang,Haotian Wang,Hongwei Wu,Xiaosheng Zheng,Fei Xie,Zhiyuan Ouyang,Weiguo Tang, Shuhong Zhang,Lili Yin,Yunqian Zhang, Peiying Meng,Xuzhen Zhu,Hongwei Zhang,Feifei Jiang, Kaiyu Zhang, Juping He,Danhong Zhang, Hanqiao Ming,Daqiao Song, Zhiping Zho,Yong Luo,Qun Gu, Yongkun Su, Xinxiao Wu,Haiyan Tang,Chenglong Wu, Weiqing Chen,Jing-Yu Liu,Wei Luo,Xuerong Huang, Shaowei Fu, Wenhai Chen, Yanbin Huang,Likang Lan, Xiaofen Zhu, Zhijun Xu, Huayun Huang, Lifeng Zhou, Zilong Chen, Minfang Lou, Binglan Wang, Yi Tan,Manlian Zhu, Weijun Hong, Feng Wang, Gonghua Pan, Aimin Shao, Weiying Li, Haijun Li, Na Zhao, Haoyu Hu, Yaxi Zhang,Mengjia Lian, Jieying Li, Xueli Cai, Zixian Luo, Yan Zhou, Xiaoyi Lu, Li Ma,Enkui Xia, Xiaoluo Zhang

Parkinsonism & related disorders (Online)/Parkinsonism & related disorders（2019）

引用15浏览0WOS引用

[A Pedigree with Dentatorubralpallidolyysian Atrophy]

Xingjiao Lu,Fei Xie,Zhidong Cen,Hongwei Wu,Xiaosheng Zheng, You Chen,Wei Luo

PubMed（2017）

引用0浏览0WOS引用

L-3-n-Butylphthalide Protects HSPB8 K141N Mutation-Induced Oxidative Stress by Modulating the Mitochondrial Apoptotic and Nrf2 Pathways

Xiao-Dong Yang,Zhi-Dong Cen,Hai-Peng Cheng, Kai Shi, Jie Bai,Fei Xie,Hong-Wei Wu,Bei-Bei Li,Wei Luo

Frontiers in Neuroscience（2017）

引用19浏览0WOS引用

Genetic Analysis Of The Tmem230 Gene In Chinese Patients With Familial Parkinson Disease

Hongwei Wu,Xiaosheng Zheng,Zhidong Cen,Fei Xie,You Chen,Xingjiao Lu,Wei Luo

PARKINSONISM & RELATED DISORDERS（2017）

引用12浏览0WOS引用

Genetic Analysis of the CHCHD2 Gene in a Cohort of Chinese Patients with Parkinson Disease

Hongwei Wu,Xingjiao Lu,Fei Xie,Zhidong Cen,Xiaosheng Zheng,Wei Luo

Neuroscience Letters（2016）

引用5浏览0WOS引用

Genetic Analysis of the CHCHD2 Gene in Chinese Patients with Familial Essential Tremor

Hongwei Wu,Xingjiao Lu,Zhidong Cen,Fei Xie,Xiaosheng Zheng,You Chen,Wei Luo

Neuroscience Letters（2016）

引用5浏览0WOS引用

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