Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation-Reference-Cited by-同舟云学术

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Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation

Published:2018-01-02 Issue:1 Volume:12 Page:54-62
ISSN:1933-6896
Container-title:Prion
language:en
Short-container-title:Prion

Author:

Akagi Akio¹²³,Iwasaki Yasushi¹,Mimuro Maya¹,Kitamoto Tetsuyuki⁴,Yamada Masahito²,Yoshida Mari¹

Affiliation:

1. Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Aichi, Japan

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

3. Department of Neurology, National Hospital Organization Iou Hospital, Kanazawa, Ishikawa, Japan

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

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336896.2017.1414130

Reference21 articles.

1. Prospective 10-year surveillance of human prion diseases in Japan

2. Clinical features of Creutzfeldt-Jakob disease with V180I mutation

3. Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene

Cited by 14 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. Altered properties of amyloidogenic prion protein in genetic Creutzfeldt–Jakob disease with PRNP V180I mutation in response to pentosan polysulfate;Brain Pathology;2023-07-31

2. V180I genetic Creutzfeldt‐Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain;Neuropathology;2023-05-10

3. Vacuoles related to tissue neuron-astrocyte ratio and infiltration of macrophages/monocytes contribute to hyperintense brain signals on diffusion-weighted magnetic resonance imaging in sporadic Creutzfeldt-Jakob disease;Journal of the Neurological Sciences;2023-04

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

5. Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt–Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene;International Journal of Molecular Sciences;2022-12-02

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