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Research article

First published 2024

Genetic and phenotypic analyses of PRRT2 positive and negative paroxysmal kinesigenic dyskinesia

Yingying Zhang, Jiechuan Ren, Tianhua Yang [...]

Therapeutic Advances in Neurological Disorders

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Research article

First published 2026

A Case of Atypical Presentation of Paroxysmal Movement Disorder,Contributed to PRRT2 Gene Variant

Mariah Pace, Doriette Soler

Journal of Child Neurology

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Research article

First published 2015-9

Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome

L. M. Zhang, Y. An, G. Pan [...]

Journal of Child Neurology

Open access

Case report

First published 2024

Three siblings with self-limited familial infantile epilepsy with PRRT2 mutation: A case series

Naoto Iwanami, Shigeru Nagaki, Aki Gen [...]

Sage Open Medical Case Reports

Free access

Other

First published 2017-5

The Role of PRRT2 in Synaptic Transmission May Not be So Benign

Matthew C. Weston

Epilepsy Currents

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Research article

First published 2016-7

The Genetics of Benign Paroxysmal Torticollis of Infancy

Meyeon Shin, Laurie M. Douglass, Jeff M. Milunsky [...]

Journal of Child Neurology

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Case report

First published 2017-11

Paroxysmal kinesigenic dyskinesia–like phenotype in multiple sclerosis

Roxana Pop, Stefan Kipfer

Multiple Sclerosis Journal

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Research article

First published 2014-11

Two novel SCN1A mutations identified in families with familial hemiplegic migraine

Claudia M Weller, Nadine Pelzer, Boukje de Vries [...]

Cephalalgia

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Research article

First published 2024-7

Misdiagnosis of functional neurological symptom disorders in paediatrics: Narrative review and relevant case report

Valentina Baglioni, Dario Esposito, Katerina Bernardi [...]

Clinical Child Psychology and Psychiatry

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