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

Benzer Materyaller

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