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Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank
Atypical progressive supranuclear palsy with corticospinal tract degeneration
Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.
White-matter integrity on DTI and the pathologic staging of Alzheimer's disease
