Alternating Hemiplegia of Childhood: Understanding the Genotype–Phenotype Relationship of ATP1A3 Variations
Author:
Publisher
Informa UK Limited
Subject
Genetics (clinical),Genetics
Reference83 articles.
1. Alternating Hemiplegia in Infants: Report of Five Cases
2. Alternating hemiplegia of childhood
3. Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
4. Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults
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1. Sleep disorders in neurological disorders and sleep-related movement disorders in children less than 2 years of age;Assessment and Treatment of Infant Sleep;2025
2. In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism;Frontiers in Neuroscience;2024-07-31
3. Navigating the Complexity of Alternating Hemiplegia in Childhood: A Comprehensive Review;Rambam Maimonides Medical Journal;2024-07-30
4. Variability of alternating hemiplegia in children;Russian neurological journal;2024-07-25
5. Contribution of the neuron-specific ATP1A3 to embryonic spinal circuit emergence;2024-06-11
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