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Works
8
Identification of missing variants by combining multiple analytic pipelines.
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank
Lewy body disease is a contributor to logopenic progressive aphasia phenotype
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
DCTN1 mutations in Perry syndrome
DNAJC13 mutations in Parkinson disease
Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study
Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population
