Frontotemporal lobar degeneration
Atrophy of the brain's frontal and temporal lobes
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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
From frontotemporal lobar degeneration pathology to frontotemporal lobar degeneration biomarkers.
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.
Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
Genotype–phenotype links in frontotemporal lobar degeneration
TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions
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