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Neurobiology of Aging|March 14, 2012
Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's diseaseSara Rollinson, Nicola Halliwell, Kate Young, et al.
Archives of Neurology|April 17, 2008
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin geneJonathan D Rohrer, Jason D Warren, Rohani Omar, et al.
Brain : a Journal of Neurology|January 13, 2006
A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17Ian R Mackenzie, Matthew Baker, Gemma West, et al.
Neurobiology of Aging|January 18, 2015
Small deletion in C9orf72 hides a proportion of expansion carriers in FTLDSara Rollinson, Janis Bennion Callister, Kate Young, et al.
Brain : a Journal of Neurology|February 4, 2012
Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutationsJulie S Snowden, Sara Rollinson, Jennifer C Thompson, et al.
Dementia and Geriatric Cognitive Disorders|November 17, 2006
Apolipoprotein E epsilon4 allele frequency and age at onset of Alzheimer's diseaseYvonne Davidson, Linda Gibbons, Antonia Pritchard, et al.
Brain : a Journal of Neurology|October 31, 2006
Mutations in progranulin explain atypical phenotypes with variants in MAPTStuart M Pickering-Brown, Matt Baker, Jenny Gass, et al.
Brain : a Journal of Neurology|October 13, 2006
Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic studyBradley F Boeve, Matt Baker, Dennis W Dickson, et al.
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