Reply to: Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report-Reference-Cited by-同舟云学术

Reply to: Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report

Published:2017-04 Issue: Volume:375 Page:489
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Hayashi Yuichi^ORCID,Inuzuka Takashi

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference6 articles.

1. Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report;Yaguchi;J. Neurol. Sci.,2017

2. Impairment of the peripheral nervous system in Creutzfeldt-Jakob disease;Niewaidomska;Arch. Neurol.,2002

3. Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion;Atarashi;Nat. Med.,2011

4. Stability and reproducibility underscore utility of RT-QuIC for diagnosis of Creutzfeldt-Jakob disease;Cramm;Mol. Neurobiol.,2016

5. CSF analysis of patients with prion disease by biomarkers and real-time qucking induced conversion (RT-QUIC) method;Satoh;Rinsho Shinkeigaku,2013

Cited by 3 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. Pathological examination is required for the case of rapidly progressive dementia with only positive result of RT-QUIC assay;Prion;2017-11-02

2. An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay;Prion;2017-07-04

3. A multidisciplinary medical network approach is crucial for increasing the number of autopsies for prion disease [Reply to: How can we increase the numbers of autopsies for prion disease? A model system in Japan];Journal of the Neurological Sciences;2017-06