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Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
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32949544 |
2020 |
| 2 |
Molecular Subtyping of PrPres in Human Sporadic CJD Brain Tissue.
61
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Klug GM...Collins SJ
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28861800 |
2017 |
| 3 |
Real-Time Quaking-Induced Conversion for Diagnosis of Prion Disease.
61
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Satoh K...Nishida N
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28861798 |
2017 |
| 4 |
Transmission characteristics of variably protease-sensitive prionopathy.
61
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Notari S...Gambetti P
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25418590 |
2014 |
| 5 |
The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease.
61
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Peden AH...Head MW
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25331173 |
2014 |
| 6 |
Molecular pathology, classification, and diagnosis of sporadic human prion disease variants.
61
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Parchi P...Saverioni D
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22505361 |
2012 |
| 7 |
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.
61
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Parchi P...Kretzschmar H
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21107851 |
2011 |
| 8 |
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.
61
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Kong Q...Gambetti P
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18234793 |
2008 |
| 9 |
Prion infections in Creutzfeldt-Jakob disease and its variants.
61
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Parker JC...Snyder JW
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1999 |
Rare neurological diseases 