Works matching IS 00016322 AND DT 2011 AND VI 121 AND IP 1
Results: 10
Molecular biology and pathology of prion strains in sporadic human prion diseases.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 79, doi. 10.1007/s00401-010-0761-3
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- Article
Tau, prions and Aβ: the triad of neurodegeneration.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 5, doi. 10.1007/s00401-010-0691-0
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The application of in vitro cell-free conversion systems to human prion diseases.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 135, doi. 10.1007/s00401-010-0708-8
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Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 113, doi. 10.1007/s00401-010-0700-3
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Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 39, doi. 10.1007/s00401-010-0713-y
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- Article
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 91, doi. 10.1007/s00401-010-0779-6
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- Article
Molecular pathology of human prion disease.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 69, doi. 10.1007/s00401-010-0735-5
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- Article
Diversity of prion diseases: (no) strains attached?
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 1, doi. 10.1007/s00401-010-0775-x
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- Article
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.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 59, doi. 10.1007/s00401-010-0656-3
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- Article
Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 21, doi. 10.1007/s00401-010-0760-4
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- Article