Rapid onset dystonia parkinsonism in a 14-year-old girl
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health
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1. Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study;The Lancet Neurology;2012-09
2. Genetic evaluation in hereditary dystonia;Handbook of Dystonia;2012-05
3. Migraine- and dystonia-related disease-mutations of Na+/K+-ATPases: Relevance of behavioral studies in mice to disease symptoms and neurological manifestations in humans;Neuroscience & Biobehavioral Reviews;2012-02
4. DYT12, Rapid Onset Dystonia-parkinsonism;Encyclopedia of Movement Disorders;2010
5. Central Procedures for Primary Dystonia;Textbook of Stereotactic and Functional Neurosurgery;2009
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