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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Neuropathological background of phenotypical variability in frontotemporal dementia
Cognition and behaviour in frontotemporal dementia with and without amyotrophic lateral sclerosis
Longitudinal evaluation of cognitive disorder in Huntington's disease
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
