frontotemporal degeneration

Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked frontotemporal dementia and amyotr...
Clinical and Pathological Diagnosis of Frontotemporal Dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease
Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups.
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Tau is a candidate gene for chromosome 17 frontotemporal dementia
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked amyotrophic lateral sclerosis-frontotemporal dem...
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Tau is a candidate gene for chromosome 17 frontotemporal dementia