@article{oai:nagoya.repo.nii.ac.jp:02001169,
 author = {Nakayama-Kamada, Chie and Enatsu, Rei and Fukumura, Shinobu and Kuribara, Tomoyoshi and Ochi, Satoko and Mikuni, Nobuhiro},
 issue = {2},
 journal = {Nagoya Journal of Medical Science},
 month = {May},
 note = {An 11-year-old male patient developed weakness or right arm elevation after sudden movement at the age of eight. Reflex epilepsy was initially suspected; however, magnetic resonance imaging and electroen-cephalography (EEG) revealed no abnormality. Video-EEG monitoring was performed, but no change was noted during attacks of weakness. He was diagnosed with paroxysmal kinesigenic dyskinesia (PKD) and carbamazepine has stopped his attacks. PKD is a rare neurological disorder characterized by brief attacks of involuntary movement triggered by sudden voluntary movements, which may be confused with reflex epilepsy. PKD should be considered as a differential diagnosis of reflex epilepsy.},
 pages = {361--365},
 title = {A case of paroxysmal kinesigenic dyskinesia suspected to be reflex epilepsy},
 volume = {83},
 year = {2021}
}