Hereditary dystonia and parkinsonism: two sides of the same coin?
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/137/9/2402/11140332/awu181.pdf
Reference8 articles.
1. Beneficial prenatal levodopa therapy in autosomal recessive guanosine triphosphate cyclohydrolase 1 deficiency;Brüggemann;Arch Neurol,2012
2. Amantadine for levodopa-induced choreic dyskinesia in compound heterozygotes for GCH1 mutations;Furukawa;Mov Disord,2004
3. Phenocopies in a large GCH1 mutation positive family with dopa responsive dystonia: confusing the picture?;Grimes;J Neurol Neurosurg Psychiatry,2002
4. Next-generation phenotyping using the parkin example: time to catch up with genetics;Grünewald;JAMA Neurol,2013
5. Primary dystonia misinterpreted as Parkinson disease: video case presentation and practical clues;Klepitskaya;Neurol Clin Practice,2013
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1. Time estimation and arousal responses in dopa-responsive dystonia;Scientific Reports;2022-08-22
2. Combined dystonias: clinical and genetic updates;Journal of Neural Transmission;2020-10-24
3. WITHDRAWN: Genetics of Parkinson’s disease;Molecular and Cellular Probes;2020-01
4. Common and rare GCH1 variants are associated with Parkinson's disease;Neurobiology of Aging;2019-01
5. ‘Atypical’ Parkinson's disease – genetic;International Review of Neurobiology;2019
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