Altered intrinsic brain activity in patients with paroxysmal kinesigenic dyskinesia by PRRT2 mutation
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Title
Altered intrinsic brain activity in patients with paroxysmal kinesigenic dyskinesia by PRRT2 mutation
Authors
Keywords
Paroxysmal kinesigenic dyskinesia (PKD), Proline-rich transmembrane protein 2 (<em class=EmphasisTypeItalic >PRRT2</em>), Mutation, C.649_650insC, Resting-state functional magnetic resonance imaging (rfMRI), Amplitude of low-frequency fluctuation (ALFF)
Journal
NEUROLOGICAL SCIENCES
Volume 34, Issue 11, Pages 1925-1931
Publisher
Springer Nature
Online
2013-03-26
DOI
10.1007/s10072-013-1408-7
References
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Note: Only part of the references are listed.- PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome
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- PRRT2 Mutations are the major cause of benign familial infantile seizures
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- Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
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- PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population
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- Hyperactive putamen in patients with paroxysmal kinesigenic choreoathetosis: A resting-state functional magnetic resonance imaging study
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- Amplitude of low-frequency oscillations in schizophrenia: A resting state fMRI study
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