Different sensorimotor mechanism in fast and slow progression amyotrophic lateral sclerosis

por Li, Qianwen, Zhu, Wenjia, Wen, Xinmei, Zang, Zhenxiang, Da, Yuwei, Lu, Jie
Publicado 2021

Beyond the Motor Cortex: Thalamic Iron Deposition Accounts for Disease Severity in Amyotrophic Lateral Sclerosis

por Li, Qianwen, Zhu, Wenjia, Wen, Xinmei, Zang, Zhenxiang, Da, Yuwei, Lu, Jie
Publicado 2022

Investigating Factors Influencing Medical Practitioners’ Resistance to and Adoption of Internet Hospitals in China: Mixed Methods Study

por Deng, Wenhao, Yang, Tianan, Deng, Jianwei, Liu, Ran, Sun, Xueqin, Li, Gang, Wen, Xinmei
Publicado 2023

A Randomized Open-Labeled Trial of Methotrexate as a Steroid-Sparing Agent for Patients With Generalized Myasthenia Gravis

por Di, Li, Shen, Faxiu, Wen, Xinmei, Lu, Yan, Zhu, Wenjia, Wang, Min, Da, Yuwei
Publicado 2022

Repeat‐associated non‐AUG translation in C9orf72‐ALS/FTD is driven by neuronal excitation and stress

por Westergard, Thomas, McAvoy, Kevin, Russell, Katelyn, Wen, Xinmei, Pang, Yu, Morris, Brandie, Pasinelli, Piera, Trotti, Davide, Haeusler, Aaron
Publicado 2019

Mortality of myasthenia gravis: a national population‐based study in China

por Zhang, Chen, Wang, Fei, Long, Zheng, Yang, Jia, Ren, Yi, Ma, Qingfeng, Li, Jiajian, Wen, Xinmei, Wang, Lijun, Da, Yuwei, Zhou, Maigeng, Yin, Peng, Hao, Junwei
Publicado 2023

A mouse model with widespread expression of the C9orf72-linked glycine–arginine dipeptide displays non-lethal ALS/FTD-like phenotypes

por Verdone, Brandie Morris, Cicardi, Maria Elena, Wen, Xinmei, Sriramoji, Sindhu, Russell, Katelyn, Markandaiah, Shashirekha S., Jensen, Brigid K., Krishnamurthy, Karthik, Haeusler, Aaron R., Pasinelli, Piera, Trotti, Davide
Publicado 2022

Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype

por Wen, Xinmei, Zhu, Wenjia, Xia, Nan L., Li, Qianwen, Di, Li, Zhang, Shu, Chen, Hai, Lu, Yan, Wang, Min, Xu, Min, Wang, Suobin, Shen, Xin-Ming, Lu, Jie, Da, Yuwei
Publicado 2021

VNTR2/VNTR3 genotype in the FCGRT gene is associated with reduced effectiveness of intravenous immunoglobulin in patients with myasthenia gravis

por Su, Shengyao, Liu, Qing, Zhang, Xueping, Wen, Xinmei, Lei, Lin, Shen, Faxiu, Fan, Zhirong, Duo, Jianying, Lu, Yan, Di, Li, Wang, Min, Chen, Hai, Zhu, Wenjia, Xu, Min, Wang, Suobin, Da, Yuwei
Publicado 2021

Synaptic dysfunction induced by glycine‐alanine dipeptides in C9orf72‐ALS/FTD is rescued by SV2 replenishment

por Jensen, Brigid K, Schuldi, Martin H, McAvoy, Kevin, Russell, Katelyn A, Boehringer, Ashley, Curran, Bridget M, Krishnamurthy, Karthik, Wen, Xinmei, Westergard, Thomas, Ma, Le, Haeusler, Aaron R, Edbauer, Dieter, Pasinelli, Piera, Trotti, Davide
Publicado 2020