Genetic prion disease: experience of a rapidly progressive dementia center in the United States and a review of the literature

Although prion diseases are generally thought to present as rapidly progressive dementias with survival of only a few months, the phenotypic spectrum for genetic prion diseases (gPrDs) is much broader. The majority have rapid decline with short survival but many present as slower progressive ataxic...

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Bibliografiska uppgifter
I publikationen:Am J Med Genet B Neuropsychiatr Genet
Huvudupphovsmän: Takada, Leonel T., Kim, Mee-Ohk, Cleveland, Ross W., Wong, Katherine, Forner, Sven A., Gala, Ignacio Illán, Fong, Jamie C., Geschwind, Michael D.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2017
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207989/
https://ncbi.nlm.nih.gov/pubmed/27943639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32505
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