Results 151 to 160 of about 201,352 (177)
DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal Lobar degeneration genetic risk-associated loci. [PDF]
Rambarack N +9 more
europepmc +1 more source
Blood inflammation relates to neuroinflammation and survival in frontotemporal lobar degeneration. [PDF]
Malpetti M +21 more
europepmc +1 more source
A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration. [PDF]
Rubio-Guerra S +17 more
europepmc +1 more source
Analysis of optineurin in frontotemporal lobar degeneration
Frontotemporal lobar degeneration (FTLD) can occur jointly with amyotrophic lateral sclerosis (ALS), and these 2 conditions share a genetic risk factor on chromosome 9. It has been reported that mutations in optineurin (OPTN) can cause ALS. Therefore, we
Anna Richardson +2 more
exaly +2 more sources
Frontotemporal lobar degeneration and ubiquitin immunohistochemistry
We set out to determine the frequency of the different pathologies underlying frontotemporal degeneration (FTD) in our brain bank series, by reviewing all cases of pathologically diagnosed FTD over the last 12 years.
Martin Rossor +2 more
exaly +2 more sources

