Involvement of striatal motoric subregions in familial frontotemporal dementia with parkinsonism harboring the C9orf72 repeat expansions
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2373-8057
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
Involvement of striatal motoric subregions in familial frontotemporal dementia with parkinsonism harboring the C9orf72 repeat expansions ; volume:8 ; number:1 ; day:6 ; month:10 ; year:2022 ; pages:1-7 ; date:12.2022
npj Parkinson's Disease ; 8, Heft 1 (6.10.2022), 1-7, 12.2022
- Creator
-
Liu, Li
Liu, Shuying
Chu, Min
Wang, Jingjuan
Xie, Kexin
Cui, Yue
Ma, Jinghong
Nan, Haitian
Cui, Chunlei
Qiao, Hongwen
Rosa-Neto, Pedro
Chan, Piu
Wu, Liyong
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1038/s41531-022-00398-5
- URN
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urn:nbn:de:101:1-2022122509100452081615
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:30 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Liu, Li
- Liu, Shuying
- Chu, Min
- Wang, Jingjuan
- Xie, Kexin
- Cui, Yue
- Ma, Jinghong
- Nan, Haitian
- Cui, Chunlei
- Qiao, Hongwen
- Rosa-Neto, Pedro
- Chan, Piu
- Wu, Liyong
- SpringerLink (Online service)
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MAPT mutation associated with frontotemporal dementia and parkinsonism (FTDP-17)
Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit
Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions
Impaired self-other differentiation in frontotemporal dementia due to the C9ORF72 expansion
Fronto-striatal alterations correlate with apathy severity in behavioral variant frontotemporal dementia
Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations
Characterization of the C9orf72 dipeptide repeat proteins in frontotemporal dementia and amyotrophic lateral sclerosis
Frontotemporal Dementia with Parkinsonism and Epilepsy Associated with VGKC Antibodies: Case Report and Literature Review
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