A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis-Reference-Cited by-同舟云学术

A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis

Published:2009-09 Issue:7 Volume:111 Page:606-609
ISSN:0303-8467
Container-title:Clinical Neurology and Neurosurgery
language:en
Short-container-title:Clinical Neurology and Neurosurgery

Author:

Iwasaki Yasushi,Kizawa Mayuki,Hori Norio,Kitamoto Tetsuyuki,Sobue Gen

Publisher

Elsevier BV

Subject

Clinical Neurology,General Medicine,Surgery

Reference15 articles.

1. Neuropathology of Gerstmann-Sträussler-Scheinker disease;Bugiani;Microsc Res Technol,2000

2. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome;Kitamoto;Biochem Biophys Res Commun,1993

3. A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis;Kitamoto;Ann Neurol,1993

4. A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease;Yamada;Neurology,1993

5. Gerstmann-Sträussler syndrome—a variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex;Amano;Acta Neuropathol (Berl),1992

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