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Detection of cutaneous prion protein deposits could help diagnose GPI-anchorless prion disease with neuropathy.

Hiroyuki HondaKosuke MatsuzonoKota SatohMasayoshi FujisawaSatoshi O SuzukiChiaki FuruyamaTetsuyuki KitamotoShigeru FujimotoKoji AbeToru Iwaki
Published in: European journal of neurology (2021)
Immunohistochemical detection of PrP in cutaneous samples could be used to definitively diagnose GPI-anchorless PrP disease with neuropathy.
Keyphrases
  • loop mediated isothermal amplification
  • platelet rich plasma
  • label free
  • real time pcr
  • small molecule