Wei Li

Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia

Shaowu Li, Yuzhi Shi, Xingao Wang, 2022, Frontiers in Neurology.

Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families

Yue Dong, Zhanjun Wang, Huapin Huang, 2021, Neuroscience Letters.

Development and Validation of a Predictive Nomogram for Possible REM Sleep Behavior Disorders

Lina Chen, Huidan Weng, Jiao Yu, 2022, Frontiers in Neurology.

A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndrome.

Wenjia Zhu, Zhanjun Wang, Junge Zhu, 2021, Parkinsonism & related disorders.

Novel mutations in HTRA1-related cerebral small vessel disease and comparison with CADASIL.

Shaowu Li, Chen Zhang, Xingao Wang, 2022, Annals of clinical and translational neurology.

Prevalence, severity, and associated factors of menopausal symptoms in middle-aged Chinese women: a community-based cross-sectional study in southeast China

Jianhong Zhou, Linjuan Ma, Yang Song, 2017, Menopause.

Two Novel Intronic Mutations in the CSF1R Gene in Two Families With CSF1R-Microglial Encephalopathy

Z. Du, Zhonghua Lu, Yaou Liu, 2022, Frontiers in Cell and Developmental Biology.

Clinical Features and Classification of Neuronal Intranuclear Inclusion Disease

H. Pan, Shao-Wei Liu, Yunzhu Pan, 2023, Neurology: Genetics.