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A multigroup approach to delayed prion production.
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- Discrete & Continuous Dynamical Systems - Series B, 2024, v. 29, n. 7, p. 1, doi. 10.3934/dcdsb.2023209
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- Article
Norwegian moose CWD induces clinical disease and neuroinvasion in gene-targeted mice expressing cervid S138N prion protein.
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- PLoS Pathogens, 2024, v. 0, n. 7, p. 1, doi. 10.1371/journal.ppat.1012350
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- Article
Longitudinal microbiome investigation throughout prion disease course reveals pre- and symptomatic compositional perturbations linked to short-chain fatty acid metabolism and cognitive impairment in mice.
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- Frontiers in Microbiology, 2024, p. 1, doi. 10.3389/fmicb.2024.1412765
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Reactive astrocytes in prion diseases: Friend or foe?
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- PLoS Pathogens, 2024, v. 20, n. 6, p. 1, doi. 10.1371/journal.ppat.1012286
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Cell adhesion molecule CD44 is dispensable for reactive astrocyte activation during prion disease.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-63464-3
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- Article
The First Genetic Characterization of the SPRN Gene in Pekin Ducks (Anas platyrhynchos domesticus).
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- Animals (2076-2615), 2024, v. 14, n. 11, p. 1588, doi. 10.3390/ani14111588
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Neuroprotective Effects of Curcumin in Neurodegenerative Diseases.
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- Foods, 2024, v. 13, n. 11, p. 1774, doi. 10.3390/foods13111774
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I<sup>123</sup>‐FP‐CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review.
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- Movement Disorders Clinical Practice, 2024, v. 11, n. 6, p. 613, doi. 10.1002/mdc3.14055
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Case Presentation of Autoimmune Septin‐5 Cerebellar Ataxia.
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- Movement Disorders Clinical Practice, 2024, v. 11, n. 6, p. 734, doi. 10.1002/mdc3.14028
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Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology.
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- Neurological Sciences, 2024, v. 45, n. 6, p. 2419, doi. 10.1007/s10072-024-07486-9
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Continuing Medical Education.
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- Transfusion, 2024, v. 64, n. 6, p. 979, doi. 10.1111/trf.17868
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- Article
Absence of evidence of transfusion transmission risk of Creutzfeldt‐Jakob disease in the United States: Results froma 28‐year lookback study.
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- Transfusion, 2024, v. 64, n. 6, p. 980, doi. 10.1111/trf.17837
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The Role of Glial Cells in Neurobiology and Prion Neuropathology.
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- Cells (2073-4409), 2024, v. 13, n. 10, p. 832, doi. 10.3390/cells13100832
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Expression of Toll-like receptors in the cerebellum during pathogenesis of prion disease.
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- Frontiers in Behavioral Neuroscience, 2024, p. 1, doi. 10.3389/fnbeh.2024.1341901
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Interactions between Cytokines and the Pathogenesis of Prion Diseases: Insights and Implications.
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- Brain Sciences (2076-3425), 2024, v. 14, n. 5, p. 413, doi. 10.3390/brainsci14050413
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- Article
RT-QuIC detection of chronic wasting disease prion in platelet samples of white-tailed deer.
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- BMC Veterinary Research, 2024, v. 20, n. 1, p. 1, doi. 10.1186/s12917-024-04005-y
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Differential expression of serum proteome on hypertensive patients with or without Sjogren's syndrome.
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- Journal of Hainan Medical University, 2024, v. 30, n. 8, p. 575, doi. 10.13210/j.cnki.jhmu.20231130.001
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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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The Role of PET Imaging in Patients with Prion Disease: A Literature Review.
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- Molecular Imaging & Biology, 2024, v. 26, n. 2, p. 195, doi. 10.1007/s11307-024-01895-0
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Gerstmann‐Sträussler‐Scheinker Disease Presenting as Late‐Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology.
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- Movement Disorders Clinical Practice, 2024, v. 11, n. 4, p. 411, doi. 10.1002/mdc3.13976
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Emerging Evidence of Golgi Stress Signaling for Neuropathies.
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- Neurology International, 2024, v. 16, n. 2, p. 334, doi. 10.3390/neurolint16020024
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- Article
Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease.
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- PLoS Pathogens, 2024, v. 20, n. 4, p. 1, doi. 10.1371/journal.ppat.1012087
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New implications for prion diseases therapy and prophylaxis.
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- Frontiers in Molecular Neuroscience, 2024, p. 1, doi. 10.3389/fnmol.2024.1324702
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Detection of prions in matching post-mortem skin and cerebrospinal fluid samples using second-generation real-time quaking-induced conversion assay.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-56789-6
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Detection limitations of prion seeding activities in blood samples from patients with sporadic prion disease.
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- BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03590-7
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Enhanced Creutzfeldt‐Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease.
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- Brain Pathology, 2024, v. 34, n. 2, p. 1, doi. 10.1111/bpa.13214
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Iatrogenic cerebral amyloid angiopathy: A multinational case series and individual patient data analysis of the literature.
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- International Journal of Stroke, 2024, v. 19, n. 3, p. 314, doi. 10.1177/17474930231203133
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- Article
Dynamic diffusion imaging changes and unique midbrain involvement in a probable MV2K sCJD.
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- Neurological Sciences, 2024, v. 45, n. 3, p. 1275, doi. 10.1007/s10072-023-07150-8
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- Article
The PINK1/Parkin pathway of mitophagy exerts a protective effect during prion disease.
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- PLoS ONE, 2024, v. 19, n. 2, p. 1, doi. 10.1371/journal.pone.0298095
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- Article
Different reactive profiles of calmodulin in the CSF samples of Chinese patients of four types of genetic prion diseases.
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- Frontiers in Molecular Neuroscience, 2024, p. 1, doi. 10.3389/fnmol.2024.1341886
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- Article
Single nucleotide polymorphisms (SNPs) in the open reading frame (ORF) of prion protein gene (PRNP) in Nigerian livestock species.
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- BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-10070-2
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Prion agents (1st section).
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- Transfusion, 2024, v. 64, p. S4, doi. 10.1111/trf.17627
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- Article
Selective Vulnerability to Neurodegenerative Disease: Insights from Cell Type-Specific Translatome Studies.
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- Biology (2079-7737), 2024, v. 13, n. 2, p. 67, doi. 10.3390/biology13020067
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- Article
Chronic Wasting Disease: State of the Science.
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- Pathogens, 2024, v. 13, n. 2, p. 138, doi. 10.3390/pathogens13020138
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Assessing Different Chronic Wasting Disease Training Aids for Use with Detection Dogs.
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- Animals (2076-2615), 2024, v. 14, n. 2, p. 300, doi. 10.3390/ani14020300
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Transcriptome analysis of the cerebral cortex of acrylamide-exposed wild-type and IL-1β-knockout mice.
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- Archives of Toxicology, 2024, v. 98, n. 1, p. 181, doi. 10.1007/s00204-023-03627-9
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Strain-Specific Targeting and Destruction of Cells by Prions.
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- Biology (2079-7737), 2024, v. 13, n. 1, p. 57, doi. 10.3390/biology13010057
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- Article
Cross-seeding by prion protein inactivates TDP-43.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 1, p. 240, doi. 10.1093/brain/awad289
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- Article
Rapidly progressive dementia due to intravascular lymphoma: A prion disease reference center experience.
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- European Journal of Neurology, 2024, v. 31, n. 1, p. 1, doi. 10.1111/ene.16068
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Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP).
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- Journal of Neurology, 2024, v. 271, n. 1, p. 263, doi. 10.1007/s00415-023-11968-9
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MRI abnormalities in Creutzfeldt–Jakob disease and other rapidly progressive dementia.
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- Journal of Neurology, 2024, v. 271, n. 1, p. 300, doi. 10.1007/s00415-023-11962-1
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Pathological findings in autoimmune encephalitis autopsy specimens from cases of suspected prion disease.
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- Journal of Neurology, 2024, v. 271, n. 1, p. 446, doi. 10.1007/s00415-023-12003-7
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- Article
Perioperative concerns in a patient with suspected Creutzfeldt - Jakob disease: A case report and review of literature.
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- Saudi Journal of Anaesthesia, 2024, v. 18, n. 1, p. 120, doi. 10.4103/sja.sja_503_23
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- Article
Analysis of the Differentially Expressed Proteins in Donkey Milk in Different Lactation Stages.
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- Foods, 2023, v. 12, n. 24, p. 4466, doi. 10.3390/foods12244466
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In Vitro and In Vivo Evidence towards Fibronectin's Protective Effects against Prion Infection.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 24, p. 17525, doi. 10.3390/ijms242417525
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Neural cell engraftment therapy for sporadic Creutzfeldt-Jakob disease restores neuroelectrophysiological parameters in a cerebral organoid model.
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- Stem Cell Research & Therapy, 2023, v. 14, n. 1, p. 1, doi. 10.1186/s13287-023-03591-2
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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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- Article
Protease-Sensitive and -Resistant Forms of Human and Murine Alpha-Synucleins in Distinct Brain Regions of Transgenic Mice (M83) Expressing the Human Mutated A53T Protein.
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- Biomolecules (2218-273X), 2023, v. 13, n. 12, p. 1788, doi. 10.3390/biom13121788
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Diagnosis in Scrapie: Conventional Methods and New Biomarkers.
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- Pathogens, 2023, v. 12, n. 12, p. 1399, doi. 10.3390/pathogens12121399
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The 11<sup>th</sup> Edition of the International Classification of Diseases and Related Health Problems: The Global Impact on the Future of Neurology for the Next Generation.
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- Turkish Journal of Neurology / Turk Noroloji Dergisi, 2023, v. 29, n. 4, p. 230, doi. 10.4274/tnd.2023.14478
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