| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann–Sträussler–Scheinker disease phenotype: comparison with similar cases from the literature
|
Jansen, Casper
|
|
2010
|
121 |
1 |
p. 59-68
|
artikel
|
| 2 |
Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease
|
Jeffrey, Martin
|
|
2010
|
121 |
1 |
p. 113-134
|
artikel
|
| 3 |
Diversity of prion diseases: (no) strains attached?
|
Brandner, Sebastian
|
|
2010
|
121 |
1 |
p. 1-4
|
artikel
|
| 4 |
Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
|
Capellari, Sabina
|
|
2010
|
121 |
1 |
p. 21-37
|
artikel
|
| 5 |
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy
|
Kovacs, Gabor G.
|
|
2010
|
121 |
1 |
p. 39-57
|
artikel
|
| 6 |
Molecular biology and pathology of prion strains in sporadic human prion diseases
|
Gambetti, Pierluigi
|
|
2010
|
121 |
1 |
p. 79-90
|
artikel
|
| 7 |
Molecular pathology of human prion disease
|
Wadsworth, Jonathan D. F.
|
|
2010
|
121 |
1 |
p. 69-77
|
artikel
|
| 8 |
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future
|
Parchi, Piero
|
|
2010
|
121 |
1 |
p. 91-112
|
artikel
|
| 9 |
Tau, prions and Aβ: the triad of neurodegeneration
|
Reiniger, Lilla
|
|
2010
|
121 |
1 |
p. 5-20
|
artikel
|
| 10 |
The application of in vitro cell-free conversion systems to human prion diseases
|
Jones, Michael
|
|
2010
|
121 |
1 |
p. 135-143
|
artikel
|
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