A case of MV2K subtype of sporadic Creutzfeldt–Jakob disease with florid‐like plaques: Similarities and differences to variant Creutzfeldt

A case of MV2K subtype of sporadic Creutzfeldt–Jakob disease with florid‐like plaques: Similarities and differences to variant Creutzfeldt–Jakob disease

Published:2020-04-05 Issue:4 Volume:40 Page:389-398
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Bošnjak Matic¹^ORCID,Zupan Andrej¹,Fiorini Michele²,Popović Katarina Š.³,Popović Mara¹^ORCID

Affiliation:

1. Faculty of Medicine Institute of Pathology, University of Ljubljana Ljubljana Slovenia

2. Department of Neurologic and Movement Sciences University of Verona Verona Italy

3. Clinical Institute of Radiology University Medical Center Ljubljana Ljubljana Slovenia

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/neup.12652

Reference59 articles.

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2. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

3. Genetic influence on the structural variations of the abnormal prion protein

4. Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future

5. Biochemical and conformational variability of human prion strains in sporadic Creutzfeldt–Jakob disease

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