Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene-Reference-Cited by-同舟云学术

Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene

Published:2018-11-02 Issue:5-6 Volume:12 Page:315-319
ISSN:1933-6896
Container-title:Prion
language:en
Short-container-title:Prion

Author:

Furukawa Fumiko¹,Sanjo Nobuo¹^ORCID,Kobayashi Atsushi²,Hamaguchi Tsuyoshi³,Yamada Masahito³,Kitamoto Tetsuyuki⁴,Mizusawa Hidehiro⁵,Yokota Takanori¹

Affiliation:

1. Department of Neurology and Neurological Science, Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences, Yushima Bunkyo-ku, Tokyo, Japan

2. Laboratory of Comparative Pathology, Hokkaido University, Graduate School of Veterinary Medicine, Kita-ku, Sapporo, Hokkaido, Japan

3. Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan

4. Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan

5. National Center of Neurology and Psychiatry, Tokyo, Japan

Funder

Ministry of Health, Labour and Welfare

Publisher

Informa UK Limited

Subject

Infectious Diseases,Cell Biology,Cellular and Molecular Neuroscience,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336896.2018.1541689

Reference15 articles.

1. Gerstmann-Straussler-Scheinker disease. I. Extending the clinical spectrum

2. An inherited prion disease with a PrP P105L mutation: Clinicopathologic and PrP heterogeneity

3. A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: A clinicopathological study

4. Gerstmann-Str�ussler syndrome ? A variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex

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3. Extracellular Protein Aggregates Colocalization and Neuronal Dystrophy in Comorbid Alzheimer’s and Creutzfeldt–Jakob Disease: A Micromorphological Pilot Study on 20 Brains;International Journal of Molecular Sciences;2021-02-20