Myoclonus-dystonia: classification, phenomenology, pathogenesis, and treatment
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference37 articles.
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2. Distribution and coexistence of myoclonus and dystonia as clinical predictors of SGCE mutation status: a pilot study;Zutt;Front Neurol,2016
3. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype;Peall;J Neurol,2014
4. Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria;Carecchio;Mov Disord,2013
5. Speech-activated myoclonus mimicking stuttering in a patient with myoclonus-dystonia syndrome;Isaacs;Tremor Other Hyperkinet Mov (N Y),2016
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1. Microstructure of the cerebellum and its afferent pathways underpins dystonia in myoclonus dystonia;European Journal of Neurology;2024-09-10
2. The natural history of progressive myoclonus ataxia;Neurobiology of Disease;2024-09
3. Next move in movement disorders: neuroimaging protocols for hyperkinetic movement disorders;Frontiers in Human Neuroscience;2024-08-30
4. Novel SGCE Mutation in a Patient With Myoclonus-Dystonia;Neurology Genetics;2024-04
5. Bilateral globus pallidus internus‐deep brain stimulation in a 5‐year‐old boy with SGCE‐related myoclonus dystonia syndrome;Pediatric Investigation;2024-03-28
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