An inherited prion disease with a PrP P105L mutation: Clinicopathologic and PrP heterogeneity-Reference-Cited by-同舟云学术

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

Published:1999-07-01 Issue:1 Volume:53 Page:181-181
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Yamada M.,Itoh Y.,Inaba A.,Wada Y.,Takashima M.,Satoh S.,Kamata T.,Okeda R.,Kayano T.,Suematsu N.,Kitamoto T.,Otomo E.,Matsushita M.,Mizusawa H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 46 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Spectrum of Tau Pathology in Human Prion Disease;Prions and Diseases;2023

2. Extracellular Prion Protein Aggregates in Nine Gerstmann–Sträussler–Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data;International Journal of Molecular Sciences;2021-12-10

3. Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene;Prion;2018-11-02

4. 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;Brain and Behavior;2018-09-21

5. Age of onset in genetic prion disease and the design of preventive clinical trials;2018-08-29

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