H
Herbert Budka
Researcher at University of Zurich
Publications - 417
Citations - 26786
Herbert Budka is an academic researcher from University of Zurich. The author has contributed to research in topics: Neuropathology & PRNP. The author has an hindex of 85, co-authored 412 publications receiving 25100 citations. Previous affiliations of Herbert Budka include Medical University of Vienna & University of Pécs.
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Journal ArticleDOI
Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome
Maria Barcikowska,Pawel P. Liberski,J. W. Boellaard,Patrick O. Brown,D. C. Gajdusek,Herbert Budka +5 more
TL;DR: It is suggested that plaques in both transmissible and nontransmissible cerebral amyloidoses seem to develop via similar pathogenetic mechanisms, irrespective of differences in etiology and molecular composition of the amyloids.
Request for updating the former SCVPH opinion on Listeria monocytogenes risk related to ready-to-eat foods and scientific advice on different levels of Listeria monocytogenes in ready-to-eat foods and the related risk for human
Olivier Andreoletti,Herbert Budka,John D. Collins,John W. Griffin,Arie Havelaar,James Hope,Günter Klein,Hilde Kruse +7 more
TL;DR: The BIOHAZ Panel concludes that after a general decline in the 1990s, the number of cases of listeriosis has increased since 2000 in Europe.
Journal ArticleDOI
Neuroaxonal pathology in Creutzfeldt-Jakob disease.
Pawel P. Liberski,Herbert Budka +1 more
TL;DR: It is concluded that neuroaxonal pathology is a frequent and important part of brain lesioning in CJD, probably reflecting profound impairment of axonal transport.
Journal ArticleDOI
Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle.
Gabor G. Kovacs,Elisabeth Lindeck-Pozza,Leila Chimelli,Abelardo Q.C. Araújo,Alberto Alain Gabbai,Thomas Ströbel,Markus Glatzel,Adriano Aguzzi,Herbert Budka +8 more
TL;DR: Using immunohistochemistry, paraffin‐embedded tissue blot, and Western blot, abundant PrPSc is demonstrated in the muscle of a patient with sporadic Creutzfeldt–Jakob disease and inclusion body myositis.
Journal ArticleDOI
Papillary glioneuronal tumor.
TL;DR: A further case of papillary glioneuronal tumor in a 12‐year‐old boy with immunohistochemical expression of PDGFRα, Olig2 and Nestin is reported, in support of a postulated origin of this tumor type from common progenitor cells in the subependymal plate.