Found: 18
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PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission study.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-41694-0
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- Publication type:
- Article
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles.
- Published in:
- 2019
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- Publication type:
- journal article
Transmission characteristics of variably protease-sensitive prionopathy.
- Published in:
- 2014
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- Publication type:
- journal article
Assessing Prion Infectivity of Human Urine in Sporadic Creutzfeldt-Jakob Disease.
- Published in:
- Emerging Infectious Diseases, 2012, v. 18, n. 1, p. 21, doi. 10.3201/eid1801.110589
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- Publication type:
- Article
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1539, doi. 10.1093/brain/awad399
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- Publication type:
- Article
Concurrent variably protease-sensitive prionopathy and amyotrophic lateral sclerosis.
- Published in:
- 2014
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- Publication type:
- Letter
Molecular biology and pathology of prion strains in sporadic human prion diseases.
- Published in:
- Acta Neuropathologica, 2011, v. 121, n. 1, p. 79, doi. 10.1007/s00401-010-0761-3
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- Publication type:
- Article
Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrP<sup>Sc</sup> types: an updated classification.
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- Acta Neuropathologica, 2009, v. 118, n. 5, p. 659, doi. 10.1007/s00401-009-0585-1
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- Publication type:
- Article
Clinicopathological Correlates in a PRNP P102L Mutation Carrier with Rapidly Progressing Parkinsonism-Dystonia.
- Published in:
- Movement Disorders Clinical Practice, 2016, v. 3, n. 4, p. 355, doi. 10.1002/mdc3.12307
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- Publication type:
- Article
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00966-x
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- Publication type:
- Article
Detection of prions in the urine of patients affected by sporadic Creutzfeldt–Jakob disease.
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- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 12, p. 2316, doi. 10.1002/acn3.51919
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- Publication type:
- Article
Multiorgan Detection and Characterization of Protease- Resistant Prion Protein in a Case of Variant CJD Examined in the United States.
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- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008765
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- Publication type:
- Article
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type.
- Published in:
- Scientific Reports, 2017, p. 38280, doi. 10.1038/srep38280
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- Publication type:
- Article
Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0734-2
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- Publication type:
- Article
Co-occurrence of chronic traumatic encephalopathy and prion disease.
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- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0643-9
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- Publication type:
- Article
Inter-Laboratory Assessment of PrP<sup>Sc</sup> Typing in Creutzfeldt–Jakob Disease: A Western Blot Study within the NeuroPrion Consortium.
- Published in:
- Brain Pathology, 2009, v. 19, n. 3, p. 384, doi. 10.1111/j.1750-3639.2008.00187.x
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- Publication type:
- Article
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.
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- Brain: A Journal of Neurology, 2010, v. 133, n. 10, p. 3030, doi. 10.1093/brain/awq234
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- Publication type:
- Article
Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein.
- Published in:
- Annals of Neurology, 2010, v. 68, n. 2, p. 162, doi. 10.1002/ana.22094
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- Publication type:
- Article