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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
BACKGROUND AND PURPOSE: The E200K mutation of the PRNP (prion protein) gene is the most common cause of familial Creutzfeldt-Jakob disease (fCJD), which has imaging and clinical features that are similar to the sporadic form. The purpose of this study was to conduct a controlled and blinded evaluati...
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| Publicado no: | AJNR Am J Neuroradiol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Neuroradiology
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8118770/ https://ncbi.nlm.nih.gov/pubmed/18635614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A1217 |
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