Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: U.K. cases 1991-2002-Reference-Cited by-同舟云学术

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Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: U.K. cases 1991-2002

Published:2004 Issue:6 Volume:55 Page:851-859
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Head Mark W.,Bunn Tristan J. R.,Bishop Matthew T.,McLoughlin Victoria,Lowrie Suzanne,McKimmie Clive S.,Williams Michelle C.,McCardle Linda,MacKenzie Jan,Knight Richard,Will Robert G.,Ironside James W.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference39 articles.

1. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

2. Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

3. A new variant of Creutzfeldt-Jakob disease in the UK

4. Laboratory diagnosis of variant Creutzfeldt-Jakob disease

5. Diagnosis of new variant Creutzfeldt-Jakob disease

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3. Development of an Automated Capillary Immunoassay to Detect Prion Glycotypes in Creutzfeldt-Jakob Disease;Laboratory Investigation;2023-03

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