Found: 31
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Generation of human chronic wasting disease in transgenic mice.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01262-y
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- Publication type:
- Article
Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo.
- Published in:
- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01132-7
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- Publication type:
- Article
A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease.
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- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00966-x
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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
Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1539, doi. 10.1093/brain/awad399
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- Publication type:
- Article
P2-207: Co-distribution of Aβ plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with E200K-129M haplotype
- Published in:
- 2008
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- Publication type:
- Abstract
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone.
- Published in:
- Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0214-2
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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
Atypical Case of VV1 Creutzfeldt–Jakob Disease Subtype: Case Report.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.875370
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- Publication type:
- Article
Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058786
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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
Human prion diseases: surgical lessons learned from iatrogenic prion transmission.
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- Neurosurgical Focus, 2016, v. 41, n. 1, p. 1, doi. 10.3171/2016.5.FOCUS15126
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- Publication type:
- Article
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.
- Published in:
- 2011
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- Publication type:
- journal 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
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, p. 1, doi. 10.1186/s40478-017-0503-z
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- Publication type:
- Article
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient.
- Published in:
- 2015
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- Publication type:
- Journal Article
Sporadic Creutzfeldt-Jakob Disease in a Native Puerto Rican Patient.
- Published in:
- Puerto Rico Health Sciences Journal, 2015, v. 34, n. 1, p. 40
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- Publication type:
- Article
Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype.
- Published in:
- Acta Neuropathologica Communications, 2023, v. 11, n. 1, p. 1, doi. 10.1186/s40478-023-01631-9
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- Publication type:
- Article
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
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- 2009
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- Publication type:
- journal article
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics.
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- Brain: A Journal of Neurology, 2009, v. 132, n. 10, p. 2643, doi. 10.1093/brain/awp196
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- Publication type:
- Article
Classification of sporadic Creutzfeldt–Jakob disease revisited.
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- Brain: A Journal of Neurology, 2006, v. 129, n. 9, p. 2266, doi. 10.1093/brain/awl224
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- Publication type:
- Article
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion.
- Published in:
- 2021
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- Publication type:
- Case Study
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
Correction: A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 1, p. 167, doi. 10.1007/s00401-023-02592-y
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- Publication type:
- Article
A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 1, p. 121, doi. 10.1007/s00401-023-02581-1
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- Publication type:
- Article
Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification.
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- Acta Neuropathologica, 2021, v. 142, n. 4, p. 707, doi. 10.1007/s00401-021-02350-y
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- Publication type:
- Article
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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- Publication type:
- Article
PMCA-replicated PrP<sup>D</sup> in urine of vCJD patients maintains infectivity and strain characteristics of brain PrP<sup>D</sup>: Transmission study.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-41694-0
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- Publication type:
- Article
Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion.
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- Frontiers in Cellular Neuroscience, 2020, v. 14, p. 1, doi. 10.3389/fncel.2020.00150
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- Publication type:
- Article