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Creutzfeldt-Jakob disease

Known as: Classic Creutzfeldt-Jakob Disease, CJD (Creutzfeldt-Jakob Disease), Creutzfeldt-Jakob Syndrome [Disease/Finding] 
A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances… 
National Institutes of Health

Papers overview

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Review
2007
Review
2007
Mitogen-activated protein kinase (MAPK) cascades are key signaling pathways involved in the regulation of normal cell… 
Highly Cited
2004
Highly Cited
2000
Highly Cited
2000
As of December 31, 1998, 35 deaths had been attributed to new variant Creutzfeldt‐Jakob disease (nvCJD) in the United Kingdom, of… 
Highly Cited
1999
Highly Cited
1999
Phenotypic heterogeneity in sporadic Creutzfeldt‐Jakob disease (sCJD) is well documented, but there is not yet a systematic… 
Highly Cited
1996
Highly Cited
1996
Highly Cited
1996
Highly Cited
1996
We sequenced the prion protein gene and studied the biochemical characteristics and the intracerebral distribution of protease… 
Highly Cited
1992
Highly Cited
1992
Fatal familial insomnia (FFI) and a subtype of familial Creutzfeldt-Jakob disease (CJD), two clinically and pathologically… 
Review
1991
Review
1991
Prions cause transmissible and genetic neurodegenerative diseases, including scrapie and bovine spongiform encephalopathy of…