rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
4
|
pubmed:dateCreated |
1993-9-28
|
pubmed:abstractText |
We report here PrP-immunohistochemistry performed on brains from CJD cases from Poland. Only one out of five definitive CJD cases exhibited typical PrP-immunoreactive kuru-like plaques and this was case of a short duration. Thus, we confirmed the low percentage of PrP plaques in CJD of Eastern and Central European origin.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0031-3114
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
42
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
115-8
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
|
pubmed:year |
1991
|
pubmed:articleTitle |
Creutzfeldt-Jakob disease (CJD) of a short duration with prion protein (PrP) plaques.
|
pubmed:affiliation |
Electron Microscopic Laboratory Dept. Oncology Medical Academy, Lód?, Poland.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|