1. Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia
    Xiaoli Liu et al, 2022, Journal of Neurology CrossRef
  2. Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant
    Yu Gu et al, 2023, Frontiers in Neurology CrossRef
  3. Evaluation of iron deposition in the motor CSTC loop of a Chinese family with paroxysmal kinesigenic dyskinesia using quantitative susceptibility mapping
    Fangfang Xie et al, 2023, Frontiers in Neurology CrossRef