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Neurodegenerative diseases and lifetime seizure risk: A study of autopsy proven cases.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.052910
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- Publication type:
- Article
In vitro amplification of ovine prions from scrapie-infected sheep from Great Britain reveals distinct patterns of propagation.
- Published in:
- BMC Veterinary Research, 2012, v. 8, n. 1, p. 223, doi. 10.1186/1746-6148-8-223
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- Publication type:
- Article
Generation of a Persistently Infected MDBK Cell Line with Natural Bovine Spongiform Encephalopathy (BSE).
- Published in:
- PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0115939
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- Publication type:
- Article
Enzymatic Formulation Capable of Degrading Scrapie Prion under Mild Digestion Conditions.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068099
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- Publication type:
- Article
Transcriptional Analysis Implicates Endoplasmic Reticulum Stress in Bovine Spongiform Encephalopathy.
- Published in:
- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014207
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- Publication type:
- Article
Evidence for a Pathogenic Role of Different Mutations at Codon 188 of PRNP.
- Published in:
- PLoS ONE, 2008, v. 3, n. 5, p. 1, doi. 10.1371/journal.pone.0002147
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- Publication type:
- Article
Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue.
- Published in:
- Acta Neuropathologica Communications, 2023, v. 11, n. 1, p. 1, doi. 10.1186/s40478-023-01534-9
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- Publication type:
- Article
Clinical findings in sporadic Creutzfeldt–Jakob disease correlate with thalamic pathology.
- Published in:
- Brain: A Journal of Neurology, 2002, v. 125, n. 11, p. 2558, doi. 10.1093/brain/awf253
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- Publication type:
- Article
Prion Protein Amino Acid Determinants of Differential Susceptibility and Molecular Feature of Prion Strains in Mice and Voles.
- Published in:
- PLoS Pathogens, 2008, v. 4, n. 7, p. 1, doi. 10.1371/journal.ppat.1000113
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- Publication type:
- Article
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene ( PRNP) and a 17-kDa prion protein fragment.
- Published in:
- Acta Neuropathologica, 2005, v. 109, n. 4, p. 443, doi. 10.1007/s00401-004-0978-0
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- Publication type:
- Article
Loss of glycosylation associated with the T183A mutation in human prion disease.
- Published in:
- Acta Neuropathologica, 2004, v. 108, n. 6, p. 476, doi. 10.1007/s00401-004-0913-4
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- Publication type:
- Article
Iatrogenic Creutzfeldt-Jakob Disease with Florid Plaques.
- Published in:
- Brain Pathology, 2003, v. 13, n. 3, p. 245, doi. 10.1111/j.1750-3639.2003.tb00025.x
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- Publication type:
- Article
The German FFI Cases.
- Published in:
- Brain Pathology, 1998, v. 8, n. 3, p. 559, doi. 10.1111/j.1750-3639.1998.tb00181.x
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- Publication type:
- Article
Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.
- Published in:
- 2018
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- Publication type:
- journal article
Clinical course in young patients with sporadic Creutzfeldt–Jakob disease.
- Published in:
- Annals of Neurology, 2005, v. 58, n. 4, p. 533
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- Publication type:
- Article
Cerebral gene expression profiles in sporadic Creutzfeldt–Jakob disease.
- Published in:
- Annals of Neurology, 2005, v. 58, n. 2, p. 242
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- Publication type:
- Article
Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene.
- Published in:
- Journal of Neurology, 2013, v. 260, n. 7, p. 1871, doi. 10.1007/s00415-013-6897-z
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- Publication type:
- Article
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia.
- Published in:
- Brain Communications, 2022, v. 4, n. 4, p. 1, doi. 10.1093/braincomms/fcac175
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- Publication type:
- Article
Seizure prevalence in neurodegenerative diseases—a study of autopsy proven cases.
- Published in:
- European Journal of Neurology, 2022, v. 29, n. 1, p. 12, doi. 10.1111/ene.15089
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- Publication type:
- Article
First symptom guides diagnosis and prognosis in neurodegenerative diseases—a retrospective study of autopsy proven cases.
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- European Journal of Neurology, 2021, v. 28, n. 6, p. 1801, doi. 10.1111/ene.14800
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- Publication type:
- Article
Single-nucleus chromatin accessibility profiling highlights distinct astrocyte signatures in progressive supranuclear palsy and corticobasal degeneration.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 4, p. 615, doi. 10.1007/s00401-022-02483-8
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- Publication type:
- Article
Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification.
- Published in:
- Acta Neuropathologica, 2021, v. 142, n. 4, p. 707, doi. 10.1007/s00401-021-02350-y
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- Publication type:
- Article
Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants.
- Published in:
- Annals of Neurology, 2000, v. 48, n. 3, p. 323, doi. 10.1002/1531-8249(200009)48:3<323::AID-ANA6>3.0.CO;2-5
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- Publication type:
- Article
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
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- Annals of Neurology, 1999, v. 46, n. 2, p. 224, doi. 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
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- Publication type:
- Article
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease.
- Published in:
- 1998
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- Publication type:
- journal article
Transcriptome analysis reveals altered cholesterol metabolism during the neurodegeneration in mouse scrapie model.
- Published in:
- Journal of Neurochemistry, 2007, v. 102, n. 3, p. 834, doi. 10.1111/j.1471-4159.2007.04566.x
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- Publication type:
- Article
Creutzfeldt-Jakob disease associated with an R148H mutation of the prion protein gene.
- Published in:
- 2005
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- Publication type:
- Letter
Substitutions of PrP N-terminal histidine residues modulate scrapie disease pathogenesis and incubation time in transgenic mice.
- Published in:
- PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0188989
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- Publication type:
- Article