Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid

Ítems similars

• Frontotemporal Lobar Degeneration with TDP-43 Proteinopathy and Chromosome 9p Repeat Expansion in C9ORF72: Clinicopathologic Correlation
  per: Bigio, Eileen H., et al.
  Publicat: (2012)
• Distribution of TDP-43 Pathology in Hippocampal Synaptic Relays Suggests Transsynaptic Propagation in Frontotemporal Lobar Degeneration
  per: Jamshidi, Pouya, et al.
  Publicat: (2020)
• TARDBP 3′-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy
  per: Gitcho, Michael A., et al.
  Publicat: (2009)
• Revisiting the utility of TDP-43 immunoreactive (TDP-43-ir) pathology to classify FTLD-TDP subtypes
  per: Nishihira, Yasushi, et al.
  Publicat: (2019)
• Spatial patterns of TDP-43 neuronal cytoplasmic inclusions (NCI) in fifteen cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)
  per: Armstrong, Richard A., et al.
  Publicat: (2011)