Literature DB >> 20038778

Discordant clinicopathologic phenotypes in a Japanese kindred of fatal familial insomnia.

Y Saitoh1, M Ogawa, Y Naito, Y Komatsuzaki, H Tagaya, K Arima, A Tamaoka, T Kitamoto, M Murata.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2010        PMID： 20038778     DOI： 10.1212/WNL.0b013e3181c7da09

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


× No keyword cloud information.
  3 in total

Review 1.  Clinical Use of Improved Diagnostic Testing for Detection of Prion Disease.

Authors:  Mark P Figgie; Brian S Appleby
Journal:  Viruses       Date:  2021-04-28       Impact factor: 5.048

2.  Fatal Familial Insomnia Initially Developing Parkinsonism Mimicking Dementia with Lewy Bodies.

Authors:  Takuya Fukuoka; Yoshihiko Nakazato; Masaomi Yamamoto; Akifumi Miyake; Takashi Mitsufuji; Toshimasa Yamamoto
Journal:  Intern Med       Date:  2018-04-27       Impact factor: 1.271

3.  Corticobasal manifestations of Creutzfeldt-Jakob disease with D178N-homozygous 129M genotype.

Authors:  Yumeng Huang; Ma Jianfang; Rodrigo Morales; Huidong Tang
Journal:  Prion       Date:  2020-12       Impact factor: 3.931
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.