Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200Lys mutation-Reference-Cited by-同舟云学术

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Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200Lys mutation

Published:1996-03-01 Issue:3 Volume:46 Page:758-761
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Chapman J.,Arlazoroff A.,Goldfarb L. G.,Cervenakova L.,Neufeld M. Y.,Werber E.,Herbert M.,Brown P.,Gajdusek D. C.,Korczyn A. D.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 61 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. Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms;Eurosurveillance;2023-12-14

2. Thalamic-insomnia phenotype in E200K Creutzfeldt–Jakob disease: A PET/MRI study;NeuroImage: Clinical;2022

3. The insomnia phenotype in genetic Creutzfeldt–Jakob disease based on the E200K mutation;Prion;2019-01-01

4. Sleep Disorders in Human Prionopathies;Current Sleep Medicine Reports;2017-07-31

5. From state dissociation to status dissociatus;Sleep Medicine Reviews;2016-08

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