First familial cases of P102L Gerstmann–Sträussler–Scheinker syndrome in South Korea: diffusion-weighted imaging might reflect intrafamilial phenotypic variability-Reference-Cited by-同舟云学术

First familial cases of P102L Gerstmann–Sträussler–Scheinker syndrome in South Korea: diffusion-weighted imaging might reflect intrafamilial phenotypic variability

Published:2022-02-07 Issue:5 Volume:43 Page:3419-3422
ISSN:1590-1874
Container-title:Neurological Sciences
language:en
Short-container-title:Neurol Sci

Author:

Ahn Seon-Jae,Lee Han Sang,Moon Jangsup,Chu Kon^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s10072-022-05927-x.pdf

Reference10 articles.

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2. Hsiao K, Baker HF, Crow TJ et al (1989) Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Nature 338(6213):342–345

3. Collins S, McLean CA, Masters CL (2001) Gerstmann-Straussler-Scheinker syndrome, fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies. J Clin Neurosci 8(5):387–397

4. Wang J, Xiao K, Zhou W, Shi Q, Dong XP (2019) Analysis of 12 Chinese patients with proline-to-leucine mutation at codon 102-associated Gerstmann-Straussler-Scheinker disease. J Clin Neurol 15(2):184–190

5. Higuma M, Sanjo N, Satoh K et al (2013) Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases. PLoS ONE 8(3):e60003

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