Isolated language impairment as the primary presentation of sporadic Creutzfeldt Jakob Disease
Author:
Affiliation:
1. National CJD Research & Surveillance Unit; University of Edinburgh; Edinburgh UK
2. Department of Clinical Neurosciences; Western General Hospital; Edinburgh UK
Funder
UK Department of Health and the Scottish Government Health Department
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ane.12600/fullpdf
Reference34 articles.
1. Prion diseases;Johnson;Lancet Neurol,2005
2. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects;Parchi;Ann Neurol,1999
3. Characteristics of established and proposed sporadic Creutzfeldt-Jakob disease variants;Appleby;Arch Neurol,2009
4. An ataxic form of subacute presenile polioencephalopathy (Creutzfeldt-Jakob disease);Brownell;J Neurol Neurosurg Psychiatry,1965
5. The ataxic form of Creutzfeldt-Jakob disease;Gomori;Arch Neurol,1973
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2. Primary progressive aphasia with focal periodic sharp wave complexes: An unusual manifestation of Creutzfeldt-Jakob disease;Clinical Neurophysiology Practice;2024
3. Three cases of Creutzfeldt–Jakob disease presenting with a predominant dysexecutive syndrome;Journal of Neurology;2022-03-01
4. Atypical and early symptoms of sporadic Creutzfeldt – Jakob disease: case series and review of the literature;International Journal of Neuroscience;2020-04-29
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