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Comprehensive clinical, radiological, pathological and biochemical analysis required to differentiate VV1 sporadic Creutzfeldt-Jakob disease from suspected variant CJD

Authors

  • Sarah Holper Department of Neurosciences, The Royal Melbourne Hospital, Parkville, Victoria, Australia PubMed articlesGoogle scholar articles
  • Victoria Lewis Australian National CJD Registry, The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, AustraliaDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Parkville, Victoria, Australia PubMed articlesGoogle scholar articles
  • Robb Wesselingh Department of Neurosciences, Alfred Hospital, Melbourne, Victoria, AustraliaMonash University Central Clinical School, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  • Frank Gaillard Faculty of Medicine Dentistry and Health Sciences, The University of Melbourne, Melbourne, Victoria, AustraliaDepartment of Radiology, The Royal Melbourne Hospital, Parkville, Victoria, Australia PubMed articlesGoogle scholar articles
  • Steven J Collins Australian National CJD Registry, The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, AustraliaDepartment of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Parkville, Victoria, Australia PubMed articlesGoogle scholar articles
  • Helmut Butzkueven Department of Neurosciences, Alfred Hospital, Melbourne, Victoria, AustraliaMonash University Central Clinical School, Melbourne, Victoria, Australia PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Sarah Holper; sarah.holper{at}mh.org.au
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Citation

Holper S, Lewis V, Wesselingh R, et al
Comprehensive clinical, radiological, pathological and biochemical analysis required to differentiate VV1 sporadic Creutzfeldt-Jakob disease from suspected variant CJD

Publication history

  • Accepted March 31, 2022
  • First published April 19, 2022.
Online issue publication 
October 18, 2023

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