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Human prion diseases with variant prion protein.
T. Kitamoto, J. Tateishi
Research output
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Contribution to journal
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Article
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peer-review
86
Citations (Scopus)
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Medicine and Dentistry
Prion Protein
100%
Transmissible Spongiform Encephalopathy
72%
Plaque
63%
Codon
63%
Central Nervous System
36%
Protein
27%
Gray Matter
18%
Myoclonus
18%
Discharge
18%
Pathogenesis
9%
Electroencephalogram
9%
Dementia
9%
Disease Course
9%
Gene
9%
Neuroscience
Prion Protein
100%
Transmissible Spongiform Encephalopathies
72%
Polymorphism
27%
Protein
27%
Myoclonus
18%
Dementia
9%
Gene
9%
Biochemistry, Genetics and Molecular Biology
Codon
63%
Nested Gene
9%
Wild Type
9%
Mutation
9%
Electroencephalogram
9%
Molecular Genetics
9%