Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration

por Cheng, Hao-Ling, Chen, Yi-Jun, Xue, Yan-Yan, Wu, Zhi-Ying, Li, Hong-Fu, Wang, Ning
Publicado 2022

Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3

por Li, Quan-Fu, Cheng, Hao‐Ling, Yang, Lu, Ma, Yin, Zhao, Jing‐Jing, Dong, Yi, Wu, Zhi‐Ying
Publicado 2020

Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias

por Cheng, Hao-Ling, Shao, Ya-Ru, Dong, Yi, Dong, Hai-Lin, Yang, Lu, Ma, Yin, Shen, Ying, Wu, Zhi-Ying
Publicado 2021

A de novo variant of POLR3B causes demyelinating Charcot-Marie-Tooth disease in a Chinese patient: a case report

por Xue, Yan-Yan, Cheng, Hao-Ling, Dong, Hai-Lin, Yin, Hou-Min, Yuan, Yun, Meng, Ling-Chao, Wu, Zhi-Ying, Yu, Hao
Publicado 2021

Neurofilament light chain is a promising serum biomarker in spinocerebellar ataxia type 3

por Li, Quan-Fu, Dong, Yi, Yang, Lu, Xie, Juan-Juan, Ma, Yin, Du, Yi-Chu, Cheng, Hao-Ling, Ni, Wang, Wu, Zhi-Ying
Publicado 2019