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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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- Article
Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment.
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- Emerging Infectious Diseases, 2012, v. 18, n. 6, p. 901, doi. 10.3201/eid1806.120116
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- Article
The Use of Real-Time Quaking-Induced Conversion for the Diagnosis of Human Prion Diseases.
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- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.874734
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- Article
Defining the phenotypic spectrum of sporadic Creutzfeldt–Jakob disease MV2K: the kuru plaque type.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 8, p. 3289, doi. 10.1093/brain/awad074
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- Publication type:
- Article
Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810210
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- Publication type:
- Article
Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt–Jakob Disease.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2051, doi. 10.3390/ijms23042051
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- Article
Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy.
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- Neuroepidemiology, 2020, v. 54, n. 1, p. 83, doi. 10.1159/000503234
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- Publication type:
- Article
The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias.
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- Alzheimer's Research & Therapy, 2018, v. 10, p. 1, doi. 10.1186/s13195-017-0331-1
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- Publication type:
- Article
Amphotericin B: A Novel Class of Antiscrapie Drugs.
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- Journal of Infectious Diseases, 1989, v. 160, n. 5, p. 795, doi. 10.1093/infdis/160.5.795
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- Publication type:
- Article
A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk.
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- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0123654
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- Article
Age at Death of Creutzfeldt-Jakob Disease in Subsequent Family Generation Carrying the E200K Mutation of the Prion Protein Gene.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060376
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- Publication type:
- Article
Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies.
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- 2009
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- Abstract
Validation of Revised International Creutzfeldt-Jakob Disease Surveillance Network Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease.
- Published in:
- JAMA Network Open, 2022, v. 5, n. 2, p. e2146319, doi. 10.1001/jamanetworkopen.2021.46319
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- Publication type:
- Article
Genetic prion disease: the EUROCJD experience.
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- Human Genetics, 2005, v. 118, n. 2, p. 166, doi. 10.1007/s00439-005-0020-1
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- Publication type:
- Article
Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier.
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- 2019
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- Publication type:
- Letter
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease.
- Published in:
- Biomolecules (2218-273X), 2020, v. 10, n. 2, p. 290, doi. 10.3390/biom10020290
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- Publication type:
- Article
Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples.
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- JAMA Neurology, 2017, v. 74, n. 2, p. 155, doi. 10.1001/jamaneurol.2016.4614
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- Publication type:
- Article
Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt–Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 10, p. 3051, doi. 10.1093/brain/aws238
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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
Ring trial of 2nd generation RT‐QuIC diagnostic tests for sporadic CJD.
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- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 11, p. 2262, doi. 10.1002/acn3.51219
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- Article
α‐Synuclein RT‐QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 10, p. 2120, doi. 10.1002/acn3.50897
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- Publication type:
- Article
Extended and direct evaluation of RT-Qu IC assays for Creutzfeldt-Jakob disease diagnosis.
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- Annals of Clinical & Translational Neurology, 2017, v. 4, n. 2, p. 139, doi. 10.1002/acn3.378
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- Publication type:
- Article
Phenotypic Heterogeneity of Variably Protease-Sensitive Prionopathy: A Report of Three Cases Carrying Different Genotypes at PRNP Codon 129.
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- Viruses (1999-4915), 2022, v. 14, n. 2, p. 367, doi. 10.3390/v14020367
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- Publication type:
- Article
Recent Italian FFI Cases.
- Published in:
- Brain Pathology, 1998, v. 8, n. 3, p. 564, doi. 10.1111/j.1750-3639.1998.tb00183.x
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- Publication type:
- Article
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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- Publication type:
- 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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- Publication type:
- Article
Concordance of cerebrospinal fluid real‐time quaking‐induced conversion across the European Creutzfeldt–Jakob Disease Surveillance Network.
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- European Journal of Neurology, 2022, v. 29, n. 8, p. 2431, doi. 10.1111/ene.15387
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- Publication type:
- Article
In reply.
- Published in:
- Transfusion, 2011, v. 51, n. 8, p. 1873, doi. 10.1111/j.1537-2995.2011.03196.x
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- Article
Transmission of sporadic Creutzfeldt-Jakob disease by blood transfusion: risk factor or possible biases.
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- Transfusion, 2011, v. 51, n. 7, p. 1556, doi. 10.1111/j.1537-2995.2010.03004.x
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- Publication type:
- Article
Performance of a seed amplification assay for misfolded alpha-synuclein in cerebrospinal fluid and brain tissue in relation to Lewy body disease stage and pathology burden.
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- Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-023-02663-0
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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
TREM2 expression in the brain and biological fluids in prion diseases.
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- Acta Neuropathologica, 2021, v. 141, n. 6, p. 841, doi. 10.1007/s00401-021-02296-1
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- Publication type:
- Article
Correction to: Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies.
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- 2020
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- Publication type:
- Correction Notice
Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies.
- Published in:
- Acta Neuropathologica, 2020, v. 140, n. 1, p. 49, doi. 10.1007/s00401-020-02160-8
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- Publication type:
- Article
Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels.
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- Acta Neuropathologica, 2017, v. 133, n. 4, p. 559, doi. 10.1007/s00401-017-1683-0
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- Publication type:
- Article
Diagnostic and prognostic performance of CSF α‐synuclein in prion disease in the context of rapidly progressive dementia.
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- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12214
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- Article
Mortality from Human Transmissible Spongiform Encephalopathies: A Record Linkage Study.
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- Neuroepidemiology, 2005, v. 24, n. 4, p. 214, doi. 10.1159/000085139
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- Publication type:
- Article
Creutzfeldt-Jakob Disease Mortality in Italy, 1982-1996.
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- Neuroepidemiology, 1999, v. 18, n. 2, p. 92, doi. 10.1159/000069412
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- Publication type:
- Article
Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect.
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- Neurogenetics, 2020, v. 21, n. 4, p. 251, doi. 10.1007/s10048-020-00618-1
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- Publication type:
- Article
Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases.
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- Molecular Neurobiology, 2019, v. 56, n. 4, p. 2811, doi. 10.1007/s12035-018-1251-1
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- Publication type:
- Article
Validation of 14-3-3 Protein as a Marker in Sporadic Creutzfeldt-Jakob Disease Diagnostic.
- Published in:
- Molecular Neurobiology, 2016, v. 53, n. 4, p. 2189, doi. 10.1007/s12035-015-9167-5
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- Publication type:
- Article
Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma.
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- Neuropathology, 2017, v. 37, n. 2, p. 110, doi. 10.1111/neup.12343
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- Publication type:
- Article