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Parkinsonism in GTP cyclohydrolase 1-deficient DOPA-responsive dystonia.

作者信息

Furukawa Yoshiaki, Kish Stephen J

机构信息

1 Department of Neurology, Juntendo Tokyo Koto Geriatric Medical Center, Tokyo, Japan 2 Department of Neurology, Faculty of Medicine, University and Postgraduate University of Juntendo, Tokyo, Japan

3 Human Brain Laboratory, Research Imaging Centre, Centre for Addiction and Mental Health, Toronto, Ontario, Canada 4 Departments of Psychiatry and Pharmacology, University of Toronto, Toronto, Ontario, Canada.

出版信息

Brain. 2015 May;138(Pt 5):e351. doi: 10.1093/brain/awu325. Epub 2014 Nov 21.

Abstract
摘要

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引用本文的文献

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Clinical and Basic Research on Dopa-Responsive Dystonia: Neuropathological and Neurochemical Findings.
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Recognizing Atypical Dopa-Responsive Dystonia and Its Mimics.
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Dopa-responsive dystonia--clinical and genetic heterogeneity.
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本文引用的文献

1
Novel DYT11 gene mutation in patients without dopaminergic deficit (SWEDD) screened for dystonia.
Neurology. 2014 Sep 23;83(13):1155-62. doi: 10.1212/WNL.0000000000000821. Epub 2014 Aug 22.
2
Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.
Brain. 2014 Sep;137(Pt 9):2480-92. doi: 10.1093/brain/awu179. Epub 2014 Jul 2.
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An international survey of patients with tetrahydrobiopterin deficiencies presenting with hyperphenylalaninaemia.
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Can SPET imaging of dopamine uptake sites replace PET imaging in Parkinson's disease? For.
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