Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism-Reference-Cited by-同舟云学术

Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism

Published:2013-09-30 Issue:1 Volume:29 Page:153-154
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Sasaki Masayuki¹,Ishii Atsushi²,Saito Yoshiaki¹,Hirose Shinichi²

Affiliation:

1. Department of Child Neurology; National Center of Neurology and Psychiatry; Kodaira Tokyo Japan

2. Department of Pediatrics and Central Research Institute for the Molecular Pathomechanisms of Epilepsy; School of Medicine, Fukuoka University; Fukuoka Japan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference8 articles.

1. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood;Heinzen;Nat Genet.,2012

2. Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study;Rosewich;Lancet Neurol.,2012

3. Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients;Ishii;PLoS One.,2013

4. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene;Brashear;Brain.,2007

5. Clinical spectrum of disease associated with ATP1A3 mutations;Ozelius;Lancet Neurol.,2012

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1. Rapid-onset dystonia-parkinsonism is associated with reduced cerebral blood flow without gray matter changes;Frontiers in Neurology;2023-01-26

2. ATP1A3 mutation in rapid-onset dystonia parkinsonism: New data and genotype-phenotype correlation analysis;Frontiers in Aging Neuroscience;2022-08-01

3. Atypical presentation of rapid-onset dystonia–parkinsonism in a toddler with a novel mutation in the ATP1A3 gene;BMJ Case Reports;2021-08

4. ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum;Frontiers in Neurology;2021-04-01

5. Auditory-perceptual voice and speech evaluation in ATP1A3 positive patients;Journal of Clinical Neuroscience;2020-11