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Combined Pathologies in FTLD-TDP Types A and C.Academic Article Why?
The relationship between schizophrenia and frontotemporal dementia.Academic Article Why?
Behavioural interventions for enhancing life participation in behavioural variant frontotemporal dementia and primary progressive aphasia.Academic Article Why?
Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.Academic Article Why?
Revisiting the utility of TDP-43 immunoreactive (TDP-43-ir) pathology to classify FTLD-TDP subtypes.Academic Article Why?
FTLD-TDP With and Without GRN Mutations Cause Different Patterns of CA1 Pathology.Academic Article Why?
Primary empathy deficits in frontotemporal dementia.Academic Article Why?
Speech and Language Presentations of FTLD-TDP Type B Neuropathology.Academic Article Why?
Corticobasal degeneration and frontotemporal dementia presentations in a kindred with nonspecific histopathology.Academic Article Why?
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy.Academic Article Why?
Frontotemporal DementiaConcept Why?
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.Academic Article Why?
Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint.Academic Article Why?
Cortical and subcortical pathological burden and neuronal loss in an autopsy series of FTLD-TDP-type C.Academic Article Why?
Primary Progressive Aphasia has a Unique Signature Distinct from Dementia of the Alzheimer's Type and Behavioral Variant Frontotemporal Dementia Regardless of Pathology.Academic Article Why?
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