| CJD | Creutzfeldt-Jakob disease |
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| CJD | CREUTZFELDT-JAKOB disease |
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| vCJD | variant CJD |
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| CJD | <abbreviation> Creutzfeldt-Jakob disease. (05 Mar 2000) |
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| CJD |
Creutzfeldt-Jakob disease: rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus; characterized by progressive dementia and gradual loss of muscle control
Ãâó: wordnet.princeton.edu/perl/webwn
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| CJD |
A rare, ultimately fatal disorder of infectious or genetic origin that typically causes memory failure and behavioral changes. A recently identified form called
Ãâó: www.alz.org/Resources/Glossary.asp
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| CJD |
(kroits ' felt - y?' k?) A disease (also known as "Classic CJD") that creates a protein plaque on the brain and eventually leads to a rapid death. It usually occurs in patients over the age of 60.
Ãâó: www.bloodbook.com/glossary.html
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| CJD |
This is a rare neurological disease thought to be caused by organic substances called prions. It has been linked to eating beef products that are contaminated with BSE.
Ãâó: www.bodyandmind.co.za/info_glossary.html
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| CJD |
A disease of humans hypothesized to be caused by a prion, or a small protein, which alters the structure of a normal brain protein, resulting in destruction of brain neural tissue. The most common form is thought to have genetic origins. There is strong epidemiologic and laboratory evidence for a causal association between new variant CJD and BSE.
Ãâó: www.csrees.usda.gov/nea/biotech/res/biotechnology_...
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| CJD | rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus |
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