Log in to save to my catalogue

Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunore...

Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunore...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A534840616

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

About this item

Full title

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

Publisher

BioMed Central Ltd

Journal title

Acta Neuropathologica Communications, 2013, Vol.1

Language

English

Formats

Publication information

Publisher

BioMed Central Ltd

More information

Scope and Contents

Contents

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. In the present study we report six patients with a novel, apparently sporadic disease characteri...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A534840616

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A534840616

Other Identifiers

ISSN

2051-5960

E-ISSN

2051-5960

DOI

10.1186/2051-5960-1-72

How to access this item