Familial Prion Disease with Alzheimer Disease-Like Tau Pathology and Clinical Phenotype

OBJECTIVE: To describe the Alzheimer disease (AD)-like clinical and pathological features, including marked neurofibrillary tangle (NFT) pathology, of a familial prion disease due to a rare nonsense mutation of the prion gene (PRNP). METHODS: Longitudinal clinical assessments were available for the...

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Detalhes bibliográficos
Main Authors: Jayadev, Suman, Nochlin, David, Poorkaj, Parvoneh, Steinbart, Ellen J., Mastrianni, James A., Montine, Thomas J., Ghetti, Bernardino, Schellenberg, Gerard D., Bird, Thomas D., Leverenz, James B.
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3114566/
https://ncbi.nlm.nih.gov/pubmed/21416485
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.22264
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