Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: A spectrum of TDP-43 proteinopathies

Eitemau Tebyg

• Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases
  gan: Geser, Felix, et al.
  Cyhoeddwyd: (2009)
• TDP-43 in Cerebrospinal Fluid of Patients With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
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  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)
• Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis
  gan: Tan, Rachel H., et al.
  Cyhoeddwyd: (2017)
• Degeneration of the locus coeruleus is a common feature of tauopathies and distinct from TDP-43 proteinopathies in the frontotemporal lobar degeneration spectrum
  gan: Ohm, Daniel T., et al.
  Cyhoeddwyd: (2020)