An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay-Reference-Cited by-同舟云学术

An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay

Published:2017-07-04 Issue:4 Volume:11 Page:284-292
ISSN:1933-6896
Container-title:Prion
language:en
Short-container-title:Prion

Author:

Hayashi Yuichi¹,Iwasaki Yasushi²,Yoshikura Nobuaki¹,Asano Takahiko³,Mimuro Maya²,Kimura Akio¹,Satoh Katsuya⁴,Kitamoto Tetsuyuki⁵,Yoshida Mari²,Inuzuka Takashi¹

Affiliation:

1. Department of Neurology and Geriatrics, Gifu University Graduate School of Medicine, Gifu, Japan

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

3. Department of Radiology, Gifu University Graduate School of Medicine, Gifu, Japan

4. Department of Locomotive Rehabilitation Sciences, Nagasaki University Graduate School of Medicine, Nagasaki, Japan

5. Division of CJD Science and Technology, Department of Prion Research, Center for Translational and Advanced Animal Research on Human Diseases, Tohoku University School of Medicine, Sendai, Japan

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/19336896.2017.1345416

Reference15 articles.

1. Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt–Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years

2. Cerebrospinal fluid tau proteins in status epilepticus

3. A prospective study of diffusion weighted magnetic resonance imaging abnormalities in patients with cluster of seizures and status epilepticus

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

5. Preserved regional cerebral blood flow in the occipital cortices, brainstem, and cerebellum of patients with V180I-129M genetic Creutzfeldt-Jakob disease in serial SPECT studies

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