Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?

BACKGROUND: Human prion diseases are a group of rare fatal neurodegenerative conditions with well-developed clinical and neuropathological diagnostic criteria. Recent observations have expanded the spectrum of prion diseases beyond the classically recognized forms. RESULTS: In the present study we r...

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Detalles Bibliográficos
Autores principales: Kovacs, Gabor G, Peden, Alexander, Weis, Serge, Höftberger, Romana, Berghoff, Anna S, Yull, Helen, Ströbel, Thomas, Koppi, Stefan, Katzenschlager, Regina, Langenscheidt, Dieter, Assar, Hamid, Zaruba, Elisabeth, Gröner, Albrecht, Voigtländer, Till, Puska, Gina, Hametner, Eva, Grams, Astrid, Muigg, Armin, Knoflach, Michael, László, Lajos, Ironside, James W, Head, Mark W, Budka, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835463/
https://www.ncbi.nlm.nih.gov/pubmed/24252716
http://dx.doi.org/10.1186/2051-5960-1-72

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835463/
https://www.ncbi.nlm.nih.gov/pubmed/24252716
http://dx.doi.org/10.1186/2051-5960-1-72

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