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Paroxysmal kinesigenic dyskinesia in a patient with a PRRT2 mutation and centrotemporal spike discharges on electroencephalogram: case report of a 10-year-old girl
Sun Young Seo, Su Jeong You
Clin Exp Pediatr. 2016;59(Suppl 1):S157-S160.   Published online November 30, 2016
DOI: https://doi.org/10.3345/kjp.2016.59.11.S157

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Paroxysmal kinesigenic dyskinesia in a patient with aPRRT2mutation and centrotemporal spike discharges on electroencephalogram: case report of a 10-year-old girl
Korean Journal of Pediatrics. 2016;59(Suppl 1):S157   Crossref logo
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Altered intrinsic brain activity in patients with paroxysmal kinesigenic dyskinesia by PRRT2 mutation
Neurological Sciences. 2013;34(11):1925-1931   Crossref logo
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Clinical features of patients with paroxysmal kinesigenic dyskinesia, mutation screening of PRRT2 and the effects of morning draughts of oxcarbazepine
BMC Pediatrics. 2019;19(1):   Crossref logo
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Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia
BMC Neurology. 2012;12(1):   Crossref logo
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A novel PRRT2 pathogenic variant in a family with paroxysmal kinesigenic dyskinesia
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PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins
European Journal of Paediatric Neurology. 2013;17(3):254-258   Crossref logo
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Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia
Movement Disorders. 2012;27(6):707-707   Crossref logo
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PRRT2 Mutation and Serum Cytokines in Paroxysmal Kinesigenic Dyskinesia
Current Medical Science. 2022;42(2):280-285   Crossref logo
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PP2.7 – 2032 Benign familial infantile epilepsy due to PRRT2 gene mutation without paroxysmal kinesigenic dyskinesia
European Journal of Paediatric Neurology. 2013;17:S35   Crossref logo
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A novel SLC20A2 mutation presenting with paroxysmal kinesigenic dyskinesia and epilepsy in a Chinese patient: a case report
Acta Neurologica Belgica. 2023;   Crossref logo
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