Deep brain stimulation for patients with dystonia in Machado–Joseph disease: three case reports
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-023-11627-z.pdf
Reference15 articles.
1. Gwinn-Hardy K, Singleton A, O’Suilleabhain P, Boss M, Nicholl D, Adam A, Hussey J, Critchley P, Hardy J, Farrer M (2001) Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family. Arch Neurol 58:296–299. https://doi.org/10.1001/archneur.58.2.296
2. Buhmann C, Bussopulos A, Oechsner M (2003) Dopaminergic response in Parkinsonian phenotype of Machado-Joseph disease. Mov Disord 18:219–221. https://doi.org/10.1002/mds.10322
3. Lu CS, Chang HC, Kuo PC, Liu YL, Wu WS, Weng YH, Yen TC, Chou YH (2004) The parkinsonian phenotype of spinocerebellar ataxia type 3 in a Taiwanese family. Parkinsonism Relat Disord 10:369–373. https://doi.org/10.1016/j.parkreldis.2004.03.009
4. Münchau A, Dressler D, Bhatia KP, Vogel P, Zühlke C (1999) Machado-Joseph disease presenting as severe generalised dystonia in a German patient. J Neurol 246:840–842. https://doi.org/10.1007/s004150050465
5. Wilder-Smith E, Tan EK, Law HY, Zhao Y, Ng I, Wong MC (2003) Spinocerebellar ataxia type 3 presenting as an L-DOPA responsive dystonia phenotype in a Chinese family. J Neurol Sci 213:25–28. https://doi.org/10.1016/s0022-510x(03)00129-1
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1. Case report: Short-term efficacy and changes in 18F-FDG-PET with acute multi-target stimulation in spinocerebellar ataxia type 3 (SCA3/MJD);Frontiers in Neurology;2023-09-27
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