1 |
Molecular Subtyping of PrPres in Human Sporadic CJD Brain Tissue.
61
|
Klug GM...Collins SJ
|
28861800 |
2017 |
2 |
Real-Time Quaking-Induced Conversion for Diagnosis of Prion Disease.
61
|
Satoh K...Nishida N
|
28861798 |
2017 |
3 |
Transmission characteristics of variably protease-sensitive prionopathy.
61
|
Notari S...Gambetti P
|
25418590 |
2014 |
4 |
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
|
Peden AH...Head MW
|
25331173 |
2014 |
5 |
Molecular pathology, classification, and diagnosis of sporadic human prion disease variants.
61
|
Parchi P...Saverioni D
|
22505361 |
2012 |
6 |
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.
61
|
Parchi P...Kretzschmar H
|
21107851 |
2011 |
7 |
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.
61
|
Kong Q...Gambetti P
|
18234793 |
2008 |
8 |
Prion infections in Creutzfeldt-Jakob disease and its variants.
61
|
Parker JC...Snyder JW
|
10219698 |
1999 |