Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred

Ítems similars

• Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
  per: Giaccone, G, et al.
  Publicat: (1992)
• Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
  per: Tagliavini, F, et al.
  Publicat: (1991)
• PET of Brain Prion Protein Amyloid in Gerstmann–Sträussler–Scheinker Disease
  per: Kepe, Vladimir, et al.
  Publicat: (2009)
• An autopsy report of three kindred in a Gerstmann–Sträussler–Scheinker disease P105L family with a special reference to prion protein, tau, and beta‐amyloid
  per: Ishizawa, Keisuke, et al.
  Publicat: (2018)
• A Case of Gerstmann-Sträussler-Scheinker Disease
  per: Park, Min Jeong, et al.
  Publicat: (2010)