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Creutzfeldt-Jakob disease
Known as:
Classic Creutzfeldt-Jakob Disease
, CJD (Creutzfeldt-Jakob Disease)
, Creutzfeldt-Jakob Syndrome [Disease/Finding]
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A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances…
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National Institutes of Health
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Related topics
Related topics
40 relations
Apathy
Aphasia
Autosomal dominant inheritance
Brain
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Narrower (4)
Creutzfeldt-Jakob Disease, Familial
Creutzfeldt-Jakob Disease, Heidenhain Variant
Creutzfeldt-Jakob Disease, Sporadic
New Variant Creutzfeldt-Jakob Disease
Broader (4)
Degenerative Diseases, Central Nervous System
Neurodegenerative Disorders
Prion Diseases
Syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2007
Review
2007
Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer
P. Roberts
,
C. Der
Oncogene
2007
Corpus ID: 3345796
Mitogen-activated protein kinase (MAPK) cascades are key signaling pathways involved in the regulation of normal cell…
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Highly Cited
1999
Highly Cited
1999
Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects
Piero Parchi
,
A. Giese
,
+15 authors
H. Kretzschmar
Annals of Neurology
1999
Corpus ID: 36024927
Phenotypic heterogeneity in sporadic Creutzfeldt‐Jakob disease (sCJD) is well documented, but there is not yet a systematic…
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Highly Cited
1999
Highly Cited
1999
Sporadic Creutzfeldt-Jakob disease: Co-occurrence of different types of PrPSc in the same brain
G. Puoti
,
G. Giaccone
,
G. Rossi
,
B. Canciani
,
O. Bugiani
,
Fabrizio Tagliavini
Neurology
1999
Corpus ID: 27023433
Article abstract Phenotypic heterogeneity of sporadic Creutzfeldt-Jakob disease (CJD) has been linked to biochemically distinct…
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Highly Cited
1996
Highly Cited
1996
A new variant of Creutzfeldt-Jakob disease in the UK
R. Will
,
J. Ironside
,
+7 authors
Peter J. Smith
The Lancet
1996
Corpus ID: 14230097
Highly Cited
1996
Highly Cited
1996
Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease
Piero Parchi
,
R. Castellani
,
+9 authors
P. Gambetti
Annals of Neurology
1996
Corpus ID: 44463521
We sequenced the prion protein gene and studied the biochemical characteristics and the intracerebral distribution of protease…
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Highly Cited
1995
Highly Cited
1995
Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)
H. Budka
,
A. Aguzzi
,
+13 authors
R. Weller
Brain Pathology
1995
Corpus ID: 41562330
Neuropathological diagnostic criteria for Creutzfeldt‐Jakob disease (CJD) and other human transmissible spongiform…
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Review
1993
Review
1993
Seeding “one-dimensional crystallization” of amyloid: A pathogenic mechanism in Alzheimer's disease and scrapie?
J. Jarrett
,
P. Lansbury
Cell
1993
Corpus ID: 11109255
Highly Cited
1992
Highly Cited
1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.
L. Goldfarb
,
R. Petersen
,
+7 authors
WW Pendelbury
Science
1992
Corpus ID: 33683590
Fatal familial insomnia (FFI) and a subtype of familial Creutzfeldt-Jakob disease (CJD), two clinically and pathologically…
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Highly Cited
1991
Highly Cited
1991
Apolipoprotein E immunoreactivity in cerebral amyloid deposits and neurofibrillary tangles in Alzheimer's disease and kuru plaque amyloid in Creutzfeldt-Jakob disease
Y. Namba
,
M. Tomonaga
,
H. Kawasaki
,
E. Otomo
,
K. Ikeda
Brain Research
1991
Corpus ID: 22526177
Review
1991
Review
1991
Molecular biology of prion diseases
S. Prusiner
Science
1991
Corpus ID: 22417182
Prions cause transmissible and genetic neurodegenerative diseases, including scrapie and bovine spongiform encephalopathy of…
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