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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
9
|
| pubmed:dateCreated |
1992-3-26
|
| pubmed:abstractText |
Human spongiform encephalopathies (HSE) are uncommon neurodegenerative diseases of unknown etiology. Whilst numerous observations provide arguments for an infectious disorder mediated by an unconventional agent of the so-called prion-type, the recent discovery of predisposing allelic variants suggests that HSE might be considered as genetically linked diseases.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0753-3322
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
45
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
379-82
|
| pubmed:dateRevised |
2005-11-16
|
| pubmed:meshHeading |
pubmed-meshheading:1786343-Animals,
pubmed-meshheading:1786343-Cattle,
pubmed-meshheading:1786343-Encephalopathy, Bovine Spongiform,
pubmed-meshheading:1786343-Humans,
pubmed-meshheading:1786343-Nerve Degeneration,
pubmed-meshheading:1786343-Nervous System Diseases,
pubmed-meshheading:1786343-Prions
|
| pubmed:year |
1991
|
| pubmed:articleTitle |
Prion diseases in man.
|
| pubmed:affiliation |
Hematology-Oncology Department, Centre Hospitalier de Luxembourg.
|
| pubmed:publicationType |
Journal Article,
Review
|