Optic nerve atrophy and visual disturbance following PRNP Y162X truncation mutation-Reference-Cited by-同舟云学术

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Optic nerve atrophy and visual disturbance following PRNP Y162X truncation mutation

Published:2021-09 Issue: Volume:428 Page:117614
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Matsuzono Kosuke,Kim Younhee,Honda Hiroyuki,Anan Yuhei,Hashimoto Yuto,Sano Ichiya,Iwaki Toru,Kitamoto Tetsuyuki,Fujimoto Shigeru

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference10 articles.

1. A novel familial prion disease causing pan-autonomic-sensory neuropathy and cognitive impairment;Matsuzono;Eur. J. Neurol.,2013

2. A novel prion disease associated with diarrhea and autonomic neuropathy;Mead;N. Engl. J. Med.,2013

3. ‘PrP systemic deposition disease’: clinical and pathological characteristics of novel familial prion disease with 2-bp deletion in codon 178;Matsuzono;Eur. J. Neurol.,2016

4. Detection of cutaneous prion protein deposits could help diagnose GPI-anchorless prion disease with neuropathy;Honda;Eur. J. Neurol.,2021

5. Prion gene PRNP Y162X truncation mutation can induce a refractory esophageal achalasia;Matsuzono;Am. J. Gastroenterol.,2021

Cited by 1 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. Prion Mutations in Republic of Republic of Korea, China, and Japan;International Journal of Molecular Sciences;2022-12-30

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