Impaired self-other differentiation in frontotemporal dementia due to the C9ORF72 expansion
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1758-9193
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Impaired self-other differentiation in frontotemporal dementia due to the C9ORF72 expansion ; volume:4 ; number:5 ; day:13 ; month:8 ; year:2012 ; pages:1-6 ; date:10.2012
Alzheimer's research & therapy ; 4, Heft 5 (13.8.2012), 1-6, 10.2012
- Creator
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Downey, Laura E.
- Contributor
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Mahoney, Colin J.
Rossor, Martin N.
Crutch, Sebastian J.
Warren, Jason D.
SpringerLink (Online service)
- DOI
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10.1186/alzrt145
- URN
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urn:nbn:de:1111-2016073131454
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:04 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Downey, Laura E.
- Mahoney, Colin J.
- Rossor, Martin N.
- Crutch, Sebastian J.
- Warren, Jason D.
- SpringerLink (Online service)
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
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Characterization of the C9orf72 dipeptide repeat proteins in frontotemporal dementia and amyotrophic lateral sclerosis
Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
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Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease
Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions
Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report
Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Serum total TDP-43 levels are decreased in frontotemporal dementia patients with C9orf72 repeat expansion or concomitant motoneuron disease phenotype
Characterization of the C9orf72 dipeptide repeat proteins in frontotemporal dementia and amyotrophic lateral sclerosis
Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration
Involvement of striatal motoric subregions in familial frontotemporal dementia with parkinsonism harboring the C9orf72 repeat expansions
Impaired β-glucocerebrosidase activity and processing in frontotemporal dementia due to progranulin mutations
Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease
Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions
Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report
Roadmap for C9ORF72 in Frontotemporal Dementia and Amyotrophic Lateral Sclerosis: Report on the C9ORF72 FTD/ALS Summit
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Serum total TDP-43 levels are decreased in frontotemporal dementia patients with C9orf72 repeat expansion or concomitant motoneuron disease phenotype
Characterization of the C9orf72 dipeptide repeat proteins in frontotemporal dementia and amyotrophic lateral sclerosis
Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
Bidirectional nucleolar dysfunction in C9orf72 frontotemporal lobar degeneration
Involvement of striatal motoric subregions in familial frontotemporal dementia with parkinsonism harboring the C9orf72 repeat expansions
Impaired β-glucocerebrosidase activity and processing in frontotemporal dementia due to progranulin mutations