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

Ítems similars

• TDP-43 in Cerebrospinal Fluid of Patients With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
  per: Steinacker, Petra, et al.
  Publicat: (2008)
• Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases
  per: Geser, Felix, et al.
  Publicat: (2009)
• 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
  per: Bigio, Eileen H, et al.
  Publicat: (2013)
• Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis
  per: Tan, Rachel H., et al.
  Publicat: (2017)
• Degeneration of the locus coeruleus is a common feature of tauopathies and distinct from TDP-43 proteinopathies in the frontotemporal lobar degeneration spectrum
  per: Ohm, Daniel T., et al.
  Publicat: (2020)