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Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding.
The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families
gene variation and microglial activity on [C]PBR28 PET in older adults at risk for Alzheimer's disease
Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [F]Flortaucipir PET
The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study
Invited review: Frontotemporal dementia caused by microtubule‐associated protein tau gene (MAPT) mutations: a chameleon for neuropathology and neuroimaging
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Association between conformational mutations in neuroserpin and onset and severity of dementia
