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Articles (11)

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1-10 of 11 results for paroxysmal kinesigenic dyskinesia

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Select article: Abnormal Somatosensory Synchronization in Patients With Paroxysmal Kinesigenic Dyskinesia: A Magnetoencephalographic Study

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Research article

First published 2017-7

Abnormal Somatosensory Synchronization in Patients With Paroxysmal Kinesigenic Dyskinesia: A Magnetoencephalographic Study

Fu-Jung Hsiao, Wan-Yu Hsu, Wei-Ta Chen [...]

Clinical EEG and Neuroscience

Select article: Genetic and phenotypic analyses of PRRT2 positive and negative paroxysmal kinesigenic dyskinesia

Open access

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

Select article: Paroxysmal kinesigenic dyskinesia–like phenotype in multiple sclerosis

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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

Select article: Review: Diagnosis and treatment of paroxysmal dyskinesias revisited

Free access

Review article

First published 2008-09

Review: Diagnosis and treatment of paroxysmal dyskinesias revisited

Iris Unterberger, Eugen Trinka

Therapeutic Advances in Neurological Disorders

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

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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

Select article: Atypical Manifestations in Glut1 Deficiency Syndrome

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Research article

First published 2016-8

Atypical Manifestations in Glut1 Deficiency Syndrome

V. De Giorgis, C. Varesio, C. Baldassari [...]

Journal of Child Neurology

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

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

Select article: Clinical commentary on “Paroxysmal kinesigenic dyskinesia-like phenotype in multiple sclerosis” and “Secondary paroxysmal dyskinesia in multiple sclerosis: Clinical-radiological features and treatment. Case report of seven patients”

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Case report

First published 2017-11

Clinical commentary on “Paroxysmal kinesigenic dyskinesia-like phenotype in multiple sclerosis” and “Secondary paroxysmal dyskinesia in multiple sclerosis: Clinical-radiological features and treatment. Case report of seven patients”

Isabel Pareés

Multiple Sclerosis Journal

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

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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

Select article: Phenotypic characterisation of paroxysmal dyskinesia in Sphynx cats

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Research article

First published 2022-6

Phenotypic characterisation of paroxysmal dyskinesia in Sphynx cats

Matthew James, Laurent Garosi, Claire Bessant [...]

Journal of Feline Medicine and Surgery

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