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Frontotemporal lobar degeneration
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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
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scientific article
Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat
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scientific article published in 2012
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
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scientific article
From frontotemporal lobar degeneration pathology to frontotemporal lobar degeneration biomarkers.
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scientific article published on April 2013
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.
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scientific article published on 12 May 2015
Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions
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article published in 2008
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
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scientific article
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
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scientific article published on 11 January 2008
Genotype–phenotype links in frontotemporal lobar degeneration
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scientific article published on 01 June 2018
TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions
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scientific article published on 01 October 2007