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Page 1
Parkinson's disease - genetic cause.
Cherian A, K P D, Vijayaraghavan A. Cherian A, et al. Curr Opin Neurol. 2023 Aug 1;36(4):292-301. doi: 10.1097/WCO.0000000000001167. Epub 2023 May 24. Curr Opin Neurol. 2023. PMID: 37366140 Review.
X-linked parkinsonism manifests at a young age accompanied by many (atypical) features such as intellectual disability, spasticity, seizures, myoclonus, dystonia, and have poor response to levodopa. SUMMARY: This review article aims to provide a comprehensive overvi …
X-linked parkinsonism manifests at a young age accompanied by many (atypical) features such as intellectual disability, spasticity, seizures …
Myoclonus: an update.
Thomas B, Frucht SJ. Thomas B, et al. Curr Opin Neurol. 2024 Aug 1;37(4):421-425. doi: 10.1097/WCO.0000000000001276. Epub 2024 May 24. Curr Opin Neurol. 2024. PMID: 38785158 Review.
We will also discuss new genetic findings associated with myoclonus-dystonia, and promising results regarding the use of perampanel in treating myoclonus. ...
We will also discuss new genetic findings associated with myoclonus-dystonia, and promising results regarding the use of peram …
SGCE Myoclonus-Dystonia: An Inherited Movement Disorder.
Yoganathan S, Kumar M, Sharma S, Patel S, Danda S, Thomas M. Yoganathan S, et al. Neurology. 2022 Feb 15;98(7):289. doi: 10.1212/WNL.0000000000013209. Epub 2021 Dec 14. Neurology. 2022. PMID: 34906973 No abstract available.
Tactile Temporal Discrimination Is Impaired in Myoclonus-Dystonia.
Tarrano C, Lamy JC, Delorme C, McGovern EM, Atkinson-Clement C, Brochard V, Thobois S, Tranchant C, Grabli D, Degos B, Corvol JC, Pedespan JM, Krystkoviak P, Houeto JL, Degardin A, Defebvre L, Apartis E, Vidailhet M, Roze E, Worbe Y. Tarrano C, et al. Mov Disord. 2020 Dec;35(12):2356-2357. doi: 10.1002/mds.28253. Epub 2020 Sep 22. Mov Disord. 2020. PMID: 32960985 No abstract available.
Serial 18F-FP-CIT and FDG PET in Fulminant Corticobasal Syndrome.
Park DG, An YS, Yoon JH. Park DG, et al. Clin Nucl Med. 2021 Sep 1;46(9):754-755. doi: 10.1097/RLU.0000000000003679. Clin Nucl Med. 2021. PMID: 34374680
Corticobasal syndrome (CBS) is characterized by a slow progressive cognitive decline, apraxia, myoclonus, dystonia, and parkinsonism. We experienced a rapidly progressing CBS patient (onset to bed-ridden within 2 years) presenting only with resting tremor but showin …
Corticobasal syndrome (CBS) is characterized by a slow progressive cognitive decline, apraxia, myoclonus, dystonia, and parkin …
74 results