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   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. The Spectrum of Self-Limited Infantile Epilepsy Syndromes
   Imad Yassin Saadeldin et al, 2024, Journal of Pediatric Epilepsy CrossRef
4. 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
5. Exploring epileptic phenotypes in PRRT2-related disorders: A report of two cases and literature appraisal
   Giovanna Scorrano et al, 2024, Seizure: European Journal of Epilepsy CrossRef