Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations
Open Access
- 15 November 2010
- journal article
- Published by Elsevier BV in NeuroImage
- Vol. 53 (3), 1070-1076
- https://doi.org/10.1016/j.neuroimage.2009.12.088
Abstract
No abstract availableKeywords
Funding Information
- Department of Health's NIHR Biomedical Research Centres
- Medical Research Council UK
- Brain Exit Scholarship
- Wellcome Trust Intermediate Clinical Fellowship
This publication has 33 references indexed in Scilit:
- Transmission and spreading of tauopathy in transgenic mouse brainNature, 2009
- Neurodegenerative Diseases Target Large-Scale Human Brain NetworksNeuron, 2009
- The role of tau in neurodegenerationMolecular Neurodegeneration, 2009
- Selective functional, regional, and neuronal vulnerability in frontotemporal dementiaCurrent Opinion in Neurology, 2008
- Mapping the progression of progranulin-associated frontotemporal lobar degenerationNature Clinical Practice Neurology, 2008
- In vivo and Postmortem Clinicoanatomical Correlations in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17Neurodegenerative Diseases, 2008
- Frontal Paralimbic Network Atrophy in Very Mild Behavioral Variant Frontotemporal DementiaArchives of Neurology, 2008
- A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesBrain, 2008
- Voxel-Based Morphometry in Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With and Without Progranulin MutationsArchives of Neurology, 2007
- Consistent resting-state networks across healthy subjectsProceedings of the National Academy of Sciences of the United States of America, 2006