Genetic Subtypes and Deep Brain Stimulation in Dystonia
Author:
Affiliation:
1. Division of Neurosurgery; Beth Israel Deaconess Medical Center; Boston MA
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mdc3.12660/fullpdf
Reference45 articles.
1. 20-year follow-up study of the neurosurgical treatment of dystonia musculorum deformans;Cooper;Adv Neurol,1976
2. Atypical presentation of rapid-onset dystonia-parkinsonism (DYT12) unresponsive to deep brain stimulation of the subthalamic nucleus;Weber;Mov Disord Clin Pract,2018
3. Failure of sequential pallidal and motor thalamus deep brain stimulation for rapid-onset dystonia-parkinsonism (DYT12);Fearon;Mov Disord Clin Pract,2018
4. Deep brain stimulation for dystonia: a novel perspective on the value of genetic testing;Jinnah;J Neural Transm,2017
5. Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystonia;Brüggemann;Neurology,2015
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