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Identifying medical mimics for late-life mania: A case of prion disease.
- Published in:
- International Journal of Psychiatry in Medicine, 2022, v. 57, n. 3, p. 202, doi. 10.1177/00912174211010529
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- Publication type:
- Article
The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.874734
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- Publication type:
- Article
Real-Time Quaking- Induced Conversion Assays for Prion Diseases, Synucleinopathies, and Tauopathies.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.853050
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- Publication type:
- Article
Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases.
- Published in:
- 2022
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- Publication type:
- journal article
Distribution of microRNA profiles in pre-clinical and clinical forms of murine and human prion disease.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-01868-x
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- Publication type:
- Article
Human Prion Disease Surveillance in Washington State, 2006-2017.
- Published in:
- JAMA Network Open, 2020, v. 3, n. 10, p. e2020690, doi. 10.1001/jamanetworkopen.2020.20690
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- Publication type:
- Article
Combinatory FK506 and Minocycline Treatment Alleviates Prion-Induced Neurodegenerative Events via Caspase-Mediated MAPK-NRF2 Pathway.
- Published in:
- International Journal of Molecular Sciences, 2019, v. 20, n. 5, p. 1144, doi. 10.3390/ijms20051144
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- Publication type:
- Article
Feasibility of Remote Assessment of Human Prion Diseases for Research and Surveillance.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2019, v. 47, n. 1/2, p. 79, doi. 10.1159/000497055
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- Publication type:
- Article
Psikiyatrik Bozuklukların Ayırıcı Tanısında Sporadik Creutzfeldt-Jakob Hastalığı: İki Olgu Sunumu.
- Published in:
- Medical Bulletin of Haseki / Haseki Tip Bulteni, 2018, v. 56, n. 3, p. 252, doi. 10.4274/haseki.99609
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- Publication type:
- Article
The proper handling of CJD-infected patient samples in the pathology laboratory.
- Published in:
- Medical Laboratory Observer (MLO), 2018, v. 50, n. 5, p. 40
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- Publication type:
- Article
Loss of prion protein induces a primed state of type I interferon-responsive genes.
- Published in:
- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0179881
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- Publication type:
- Article
Selective propagation of mouse-passaged scrapie prions with long incubation period from a mixed prion population using GT1-7 cells.
- Published in:
- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0179317
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- Publication type:
- Article
Prion Diagnosis: Application of Real-Time Quaking-Induced Conversion.
- Published in:
- BioMed Research International, 2017, v. 2017, p. 1, doi. 10.1155/2017/5413936
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- Publication type:
- Article
Protease resistance of infectious prions is suppressed by removal of a single atom in the cellular prion protein.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0170503
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- Publication type:
- Article
Cystatin F is a biomarker of prion pathogenesis in mice.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171923
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- Publication type:
- Article
Diagnostic and prognostic value of human prion detection in cerebrospinal fluid.
- Published in:
- 2017
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- Publication type:
- journal article
Comparison of Two US Sheep Scrapie Isolates Supports Identification as Separate Strains.
- Published in:
- Veterinary Pathology, 2016, v. 53, n. 6, p. 1187, doi. 10.1177/0300985816629712
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- Publication type:
- Article
From Scientific Curiosity to Public Enemy Number One in Six Short Months.
- Published in:
- PLoS Pathogens, 2016, v. 12, n. 4, p. 1, doi. 10.1371/journal.ppat.1005371
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- Publication type:
- Article
Clinical findings and diagnosis in genetic prion diseases in Germany.
- Published in:
- European Journal of Epidemiology, 2016, v. 31, n. 2, p. 187, doi. 10.1007/s10654-015-0049-y
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- Publication type:
- Article
Gerstmann-Sträussler-Scheinker Disease Presenting with Atypical Parkinsonism, but Typical Magnetic Resonance Imaging Findings of Prion Disease.
- Published in:
- Movement Disorders Clinical Practice, 2016, v. 3, n. 1, p. 93, doi. 10.1002/mdc3.12228
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- Publication type:
- Article
A Difficult Diagnosis in Emergency Department: Creutzfeldt-Jakob Disease.
- Published in:
- 2015
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- Publication type:
- Case Study
Downregulation of β-Soluble N-Ethylmaleimide-Sensitive Factor Attachment Protein: Proteomics-Based Identification in Early-Stage Prion Disease.
- Published in:
- Neurodegenerative Diseases, 2015, v. 15, n. 4, p. 193, doi. 10.1159/000371553
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- Publication type:
- Article
New Diagnostic Methods for Creutzfeldt-Jakob Disease.
- Published in:
- Neurology Alert, 2014, v. 34, n. 3, p. 20
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- Publication type:
- Article
بررسی تأثیر تغییرات درجهي حرارت بر کنفورماسیون پروتئین پریون انسانی به روش شبیهسازي دینامیک مولکولی
- Published in:
- Arak Medical University Journal, 2014, v. 17, n. 7, p. 48
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- Publication type:
- Article
Detection of Infectivity in Blood of Persons with Variant and Sporadic Creutzfeldt-Jakob Disease.
- Published in:
- Emerging Infectious Diseases, 2014, v. 20, n. 1, p. 114, doi. 10.3201/eid2001.130353
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- Publication type:
- Article
Protein Misfolding and Neurodegenerative Diseases.
- Published in:
- International Journal of Cell Biology, 2014, p. 1, doi. 10.1155/2014/217371
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- Publication type:
- Article
Prion diseases and sleep disorders.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2013, v. 13, n. 6, p. 471, doi. 10.3969/j.issn.1672-6731.2013.06.002
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- Publication type:
- Article
Human prion diseases: progress in clinical trials.
- Published in:
- Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 996, doi. 10.1093/brain/awt075
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- Publication type:
- Article
Detection of prion protein oligomers by single molecule fluorescence imaging.
- Published in:
- Neuropathology, 2013, v. 33, n. 1, p. 1, doi. 10.1111/j.1440-1789.2012.01316.x
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- Publication type:
- Article
A Visual Dual-Aptamer Logic Gate for Sensitive Discrimination of Prion Diseases-Associated Isoform with Reusable Magnetic Microparticles and Fluorescence Quantum Dots.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0053935
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- Publication type:
- Article
Behavior of Prions in the Environment: Implications for Prion Biology.
- Published in:
- PLoS Pathogens, 2013, v. 9, n. 2, p. 1, doi. 10.1371/journal.ppat.1003113
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- Publication type:
- Article
Identification of Misfolded Proteins in Body Fluids for the Diagnosis of Prion Diseases.
- Published in:
- International Journal of Cell Biology, 2013, p. 1, doi. 10.1155/2013/839329
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- Publication type:
- Article
Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054915
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- Publication type:
- Article
The Epidemiological, Clinical, and Laboratory Features of Sporadic Creutzfeldt-Jakob Disease Patients in China: Surveillance Data from 2006 to 2010.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0024231
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- Publication type:
- Article
The Observatory. New studies.
- Published in:
- Medical Laboratory Observer (MLO), 2011, v. 43, n. 3, p. 6
- Publication type:
- Article
Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays.
- Published in:
- PLoS Pathogens, 2010, v. 6, n. 12, p. 1, doi. 10.1371/journal.ppat.1001217
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- Publication type:
- Article
The Japanese Society of Neuropathology.
- Published in:
- 2010
- Publication type:
- Abstract
Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study.
- Published in:
- Brain: A Journal of Neurology, 2009, v. 132, n. 10, p. 2669, doi. 10.1093/brain/awp210
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- Publication type:
- Article
Abnormal Brain Iron Homeostasis in Human and Animal Prion Disorders.
- Published in:
- PLoS Pathogens, 2009, v. 5, n. 3, p. 1, doi. 10.1371/journal.ppat.1000336
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- Publication type:
- Article
Simplified ultrasensitive prion detection by recombinant PrP conversion with shaking.
- Published in:
- 2008
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- Publication type:
- Letter
Identification of genes differentially expressed in SH-SY5Y neuroblastoma cells exposed to the prion peptide 106–126.
- Published in:
- European Journal of Neuroscience, 2007, v. 26, n. 1, p. 51, doi. 10.1111/j.1460-9568.2007.05646.x
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- Publication type:
- Article
Test for early detection of BSE, vCJD on horizon?
- Published in:
- Canadian Medical Association Journal (CMAJ), 2001, v. 165, n. 2, p. 199
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- Publication type:
- Article
Diagnosis of prion diseases soon possible?
- Published in:
- WHO Drug Information, 2001, v. 15, n. 2, p. 67
- Publication type:
- Article
CorrespondenceUniversal leucodepletion to reduce potential risk of transmission of new-variant creutzfeld–jakob disease.
- Published in:
- British Journal of Haematology, 2000, v. 110, n. 3, p. 745, doi. 10.1046/j.1365-2141.2000.02239-3.x
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- Publication type:
- Article
CORRESPONDENCEEXPRESSION OF CELL-ASSOCIATED PRION PROTEIN ON NORMAL HUMAN PLATELETS – REPLY.
- Published in:
- British Journal of Haematology, 2000, v. 110, n. 3, p. 749, doi. 10.1046/j.1365-2141.2000.02239-6.x
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- Publication type:
- Article
Prion protein immunoreactivity in brain samples from an unselected autopsy population: findings in 200 consecutive cases.
- Published in:
- Neuropathology & Applied Neurobiology, 2000, v. 26, n. 3, p. 273, doi. 10.1046/j.1365-2990.2000.00239.x
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- Publication type:
- Article