Literature DB >> 23577611

Sporadic Creutzfeldt-Jakob disease presenting as spastic paraparesis.

N Geevasinga, N G Simon, S Collins, M E Buckland, K Ng.   

Abstract

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Year:  2013        PMID： 23577611     DOI： 10.1111/ene.12116

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN： 1351-5101            Impact factor:   6.089


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  2 in total

1.  The insomnia phenotype in genetic Creutzfeldt-Jakob disease based on the E200K mutation.

Authors:  Eva Feketeova; Dominika Jarcuskova; Alzbeta Janakova; Marianna Vitkova; Jozef Dragasek; Zuzana Gdovinova
Journal:  Prion       Date:  2019-01       Impact factor: 3.931

2.  A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset.

Authors:  Taichi Nomura; Ikuko Iwata; Ryoji Naganuma; Masaaki Matsushima; Katsuya Satoh; Tetsuyuki Kitamoto; Ichiro Yabe
Journal:  Prion       Date:  2020-12       Impact factor: 3.931
  2 in total

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