ALS and FTLD: two faces of TDP-43 proteinopathy

Documenti analoghi

• 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
  di: Bigio, Eileen H, et al.
  Pubblicazione: (2013)
• Spatial patterns of TDP-43 neuronal cytoplasmic inclusions (NCI) in fifteen cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)
  di: Armstrong, Richard A., et al.
  Pubblicazione: (2011)
• A QUANTITATIVE STUDY OF THE NEUROPATHOLOGY OF THIRTY-TWO SPORADIC AND FAMILIAL CASES OF FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP-43 PROTEINOPATHY (FTLD-TDP)
  di: Armstrong, Richard A., et al.
  Pubblicazione: (2012)
• Hippocampal sclerosis in Lewy body disease is a TDP-43 proteinopathy similar to FTLD-TDP Type A
  di: Aoki, Naoya, et al.
  Pubblicazione: (2014)
• Towards a TDP-43-Based Biomarker for ALS and FTLD
  di: Feneberg, Emily, et al.
  Pubblicazione: (2018)