Prion diseases: an introduction-Reference-Cited by-同舟云学术

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Prion diseases: an introduction

Published:2013-10-01 Issue: Volume: Page:231-254
ISSN:1871-9295
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Author:

Budka Herbert¹²,Gelpi Ellen¹²

Affiliation:

1. Institute of Neuropathology, University Hospital Zurich, Schmelzbergstr. 12, 8091 Zurich, Switzerland; and Institute of Neurology, Medical University of Vienna, Austria

2. Neurological Tissue Bank of the Biobank-Hospital Clinic-IDIBAPS, Facultad de Medicina, c/Casanova 143, planta 0, ala sur, 08036 Barcelona, Spain

Publisher

Wageningen Academic Publishers

Link

https://www.wageningenacademic.com/doi/pdf/10.3920/978-90-8686-780-6_11

Reference145 articles.

1. Gerstmann-Str�ussler syndrome ? A variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex

2. Gerstmann-Str�ussler syndrome ? A variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex

3. Armstrong, R.A., 2010. Laminar distribution of the pathological changes in sporadic and variant Creutzfeldt-Jakob disease. Patholog. Res. Int. 16(2011), 236346.

4. Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Str�ussler-Scheinker syndrome

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