A QUANTITATIVE STUDY OF THE NEUROPATHOLOGY OF THIRTY-TWO SPORADIC AND FAMILIAL CASES OF FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP-43 PROTEINOPATHY (FTLD-TDP)

Eitemau Tebyg

• Spatial patterns of TDP-43 neuronal cytoplasmic inclusions (NCI) in fifteen cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)
  gan: Armstrong, Richard A., et al.
  Cyhoeddwyd: (2011)
• Fine structural analysis of the neuronal inclusions of frontotemporal lobar degeneration with TDP-43 proteinopathy
  gan: Thorpe, Julian R., et al.
  Cyhoeddwyd: (2008)
• 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
  gan: Bigio, Eileen H, et al.
  Cyhoeddwyd: (2013)
• TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration with Ubiquitin Inclusions
  gan: Cairns, Nigel J., et al.
  Cyhoeddwyd: (2007)
• LAMINAR DISTRIBUTION OF THE PATHOLOGICAL CHANGES IN SPORADIC FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP-43 PROTEINOPATHY: A QUANTITATIVE STUDY USING POLYNOMIAL CURVE FITTING
  gan: Armstrong, Richard A., et al.
  Cyhoeddwyd: (2013)