Effect of Comprehensive Cerebral Protection Program on Cerebral Oxygen Metabolism and Vascular Endothelial Function in Elderly Patients with Acute Cerebral Infarction

por ZHOU, Meihong, HUANG, Zhaojun
Publicado 2019

Case report: Reversible encephalopathy associated with liposomal amphotericin B in a patient with cryptococcal meningitis

por Luo, Si, Wen, Han, Zhou, Meihong, Wu, Chengsi, Hong, Daojun
Publicado 2022

A comparison of random survival forest and Cox regression for prediction of mortality in patients with hemorrhagic stroke

por Wang, Yuxin, Deng, Yuhan, Tan, Yinliang, Zhou, Meihong, Jiang, Yong, Liu, Baohua
Publicado 2023

Sturge-Weber syndrome coexisting with episodes of rhabdomyolysis

por Zhu, Min, Li, Xiaobin, Zhou, Meihong, Wan, Hui, Wu, Yuchen, Hong, Daojun
Publicado 2013

Anti-dipeptidyl-peptidase-like protein 6 encephalitis with pure cerebellar ataxia: a case report

por Lin, Jing, Zhu, Min, Mao, Xiaocheng, Jin, Zeqing, Zhou, Meihong, Hong, Daojun
Publicado 2022

Human viral encephalitis associated with suid herpesvirus 1

por Zhou, Yiyi, Nie, Chong, Wen, Han, Long, Yong, Zhou, Meihong, Xie, Zunchun, Hong, Daojun
Publicado 2021

The Alterations of Cortical Volume, Thickness, Surface, and Density in the Intermediate Sporadic Parkinson's Disease from the Han Population of Mainland China

por Deng, Xia, Zhou, Meihong, Tang, Chunyan, Zhang, Jie, Zhu, Lei, Xie, Zunchun, Gong, Honghan, Xiao, Xiangzuo, Xu, Renshi
Publicado 2016

Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutation

por Jiang, Kaiyan, Zheng, Yilei, Lin, Jing, Wu, Xiaorong, Yu, Yanyan, Zhu, Min, Fang, Xin, Zhou, Meihong, Li, Xiaobing, Hong, Daojun
Publicado 2022

Juvenile-onset PSAT1-related neuropathy: A milder phenotype of serine deficiency disorder

por Shen, Yu, Peng, Yun, Huang, Pengcheng, Zheng, Yilei, Li, Shumeng, Jiang, Kaiyan, Zhou, Meihong, Deng, Jianwen, Zhu, Min, Hong, Daojun
Publicado 2022

Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy

por Wu, Chengsi, Xiang, Haijie, Chen, Ran, Zheng, Yilei, Zhu, Min, Chen, Shuyun, Yu, Yanyan, Peng, Yun, Yu, Yaqing, Deng, Jianwen, Zhou, Meihong, Hong, Daojun
Publicado 2022

FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders

por Zhou, Binbin, Wang, Huan, Cai, Yu, Wen, Han, Wang, Lulu, Zhu, Min, Chen, Yunqing, Yu, Yanyan, Lu, Xi, Zhou, Meihong, Fang, Pu, Li, Xiaobing, Hong, Daojun
Publicado 2020

Benign monomelic amyotrophy of lower limb in a cohort of chinese patients

por Wang, Lulu, Wen, Han, Chen, Shuyun, Wang, Huan, Zheng, Yilei, Chen, Ran, Li, Jingjing, Jiang, Kaiyan, Xiang, Haijie, Zhu, Min, Zhou, Meihong, Yao, Sheng, Hong, Daojun
Publicado 2021