An autopsy case of Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction-Reference-Cited by-同舟云学术

An autopsy case of Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction

Published:2017-07-13 Issue:6 Volume:37 Page:575-581
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Iwasaki Yasushi¹^ORCID,Mori Keiko²,Ito Masumi²,Akagi Akio¹,Mimuro Maya¹,Kitamoto Tetsuyuki³,Yoshida Mari¹

Affiliation:

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

2. Department of Neurology; Oyamada Memorial Spa Hospital; Yokkaichi Japan

3. Department of Neurological Science; Tohoku University Graduate School of Medicine; Sendai Japan

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12399/fullpdf

Reference24 articles.

1. Creutzfeldt-Jakob disease;Iwasaki;Neuropathology,2017

2. Sporadic and familial CJD: classification and characterization;Gambetti;Br Med Bull,2003

3. Genetic prion disease: the EUROCJD experience;Kovács;Hum Genet,2005

4. Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt-Jakob disease: proposed staging of cerebral cortical pathology;Iwasaki;J Neurol Sci,2014

5. Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type;Iwasaki;Acta Neuropathol,2006

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

3. 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

4. Clinicopathological findings of a long-term survivor of V180I genetic Creutzfeldt-Jakob disease;Prion;2020-01-01

5. A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset;Prion;2020-01-01