Works matching DE "CREUTZFELDT-Jakob disease"
Results: 2040
Bovine spongiform encephalopathy: A review of current knowledge and challenges.
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- Open Veterinary Journal, 2025, v. 15, n. 1, p. 54, doi. 10.5455/OVJ.2025.v15.i1.5
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- Article
Creutzfeldt-Jakob disease − A case report.
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- 2025
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- Case Study
Ten-year mortality from Creutzfeldt-Jakob disease in Cyprus.
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- Eastern Mediterranean Health Journal, 2008, v. 14, n. 3, p. 715
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- Article
Creutzfeldt-Jakob disease in Slovenia from 1985 to 2003.
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- Wiener Klinische Wochenschrift, 2004, v. 116, n. 15/16, p. 524, doi. 10.1007/BF03217705
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- Article
Species variation in PrP<sup>Sc</sup> protofibril models.
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- Journal of Materials Science, 2008, v. 43, n. 10, p. 3625, doi. 10.1007/s10853-008-2578-1
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- Article
Prions and Orthopedic Surgery.
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- Infection, 2003, v. 31, n. 3, p. 163
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- Article
Neuropathological characterisation of French bovine spongiform encephalopathy cases.
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- Histochemistry & Cell Biology, 2003, v. 120, n. 6, p. 513, doi. 10.1007/s00418-003-0593-5
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- Article
Toluidine blue-O staining of prion protein deposits.
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- Histochemistry & Cell Biology, 2001, v. 116, n. 6, p. 519, doi. 10.1007/s00418-001-0343-5
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- Article
Paracelsus and the cranberries.
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- 1998
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- Editorial
A CONTRIBUIÇÃO GENÉTICA NO DESENVOLVIMENTO DE DOENÇAS PRIÔNICAS: REVISÃO SISTEMÁTICA.
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- Revista Foco (Interdisciplinary Studies Journal), 2023, v. 16, n. 6, p. 1, doi. 10.54751/revistafoco.v16n6-096
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- Article
Fighting the good fight in Europe.
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- 2005
- Publication type:
- Editorial
A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis.
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- Human Genetics, 2020, v. 139, n. 4, p. 461, doi. 10.1007/s00439-019-02102-9
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- Article
Comparison of machine learning approaches for enhancing Alzheimer's disease classification.
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- PeerJ, 2021, p. 1, doi. 10.7717/peerj.10549
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- Article
Use of competing conceptions of risk in animal agriculture.
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- Journal of Animal Science, 1998, v. 76, n. 3, p. 706, doi. 10.2527/1998.763706x
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- Article
A Case of Creutzfeldt–Jakob disease with psychiatric presentation.
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- Journal of Geriatric Mental Health, 2024, v. 11, n. 1, p. 60, doi. 10.4103/jgmh.jgmh_15_24
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- Article
Synthesis and anti-prion aggregation activity of acylthiosemicarbazide analogues.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2191164
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- Article
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
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
Sensory disturbances in Creutzfeldt-Jakob disease.
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- Neurological Sciences, 2024, v. 45, n. 3, p. 1057, doi. 10.1007/s10072-023-07093-0
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- Article
Anti-NMDA receptor encephalitis with "Hockey stick sign" mimicking CJD.
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- Neurological Sciences, 2023, v. 44, n. 2, p. 741, doi. 10.1007/s10072-022-06455-4
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- Article
Presence of anti-IgLON5 antibody in a case of sporadic Creutzfeldt–Jakob disease with sleep disturbance as a prominent symptom.
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- Neurological Sciences, 2023, v. 44, n. 2, p. 737, doi. 10.1007/s10072-022-06434-9
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- Article
Correction to: The cognitive phenotypes of Creutzfeldt‑Jakob disease: comparison with secondary metabolic encephalopathy.
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- Neurological Sciences, 2022, v. 43, n. 11, p. 6609, doi. 10.1007/s10072-021-05795-x
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- Article
Epidemiological and clinical characteristics of patients with late-onset Creutzfeldt-Jakob disease.
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- 2022
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- journal article
The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy.
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- Neurological Sciences, 2022, v. 43, n. 6, p. 3703, doi. 10.1007/s10072-021-05795-x
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Early and long-term cognitive features in sporadic Creutzfeldt-Jakob disease.
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- 2021
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- Letter
Tics in patients with encephalitis.
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- Neurological Sciences, 2021, v. 42, n. 4, p. 1311, doi. 10.1007/s10072-021-05065-w
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- Article
A new neurobehavioral phenotype of familial Creutzfeldt-Jakob disease: impaired theory of mind.
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- 2019
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- Case Study
Sporadic Creutzfeldt-Jakob disease presenting with isolated progressive non-fluent aphasia in a young woman.
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- 2017
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- Case Study
Autopsy-like MRI findings: report on Creutzfeldt-Jakob disease in the end-stage.
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- 2015
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- Letter
Familial Creutzfeldt-Jakob disease with M232R mutation presented with corticobasal syndrome.
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- 2015
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- Letter
Corticobasal syndrome-like variant of Creutzfeldt-Jakob disease: clinical description of two cases.
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- 2015
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- Publication type:
- Letter
Leptomeningeal carcinomatosis mimicking Creutzfeldt-Jakob disease: clinical features, laboratory tests, MRI images, EEG findings in an autopsy-proven case.
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- Neurological Sciences, 2013, v. 34, n. 4, p. 441, doi. 10.1007/s10072-012-1021-1
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- Article
Current state and in vitro conservation of the only endangered population of Corylus avellana in Kazakhstan.
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- Research on Crops, 2020, v. 21, n. 4, p. 681, doi. 10.31830/2348-7542.2020.106
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- Article
Creutzfeldt-Jakob disease: a single institution case series.
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- International Journal of Palliative Nursing, 2024, v. 30, n. 12, p. 630, doi. 10.12968/ijpn.2024.30.12.630
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- Article
Total Tau Protein in Cerebrospinal Fluid and Diffusion-Weighted MRI as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease.
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- Dementia & Geriatric Cognitive Disorders, 2007, v. 24, n. 3, p. 207, doi. 10.1159/000107082
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Chronological Changes in MRI and CSF Biochemical Markers in Creutzfeldt-Jakob Disease Patients.
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- Dementia & Geriatric Cognitive Disorders, 2007, v. 23, n. 6, p. 372, doi. 10.1159/000101339
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- Article
Proteomic Analysis of the Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease.
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- Dementia & Geriatric Cognitive Disorders, 2006, v. 23, n. 1, p. 22, doi. 10.1159/000096589
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- Article
Presymptomatic Signs in Healthy CJD Mutation Carriers.
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- Dementia & Geriatric Cognitive Disorders, 2005, v. 19, n. 5/6, p. 246, doi. 10.1159/000084549
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- Article
Follow-Up Investigations of Tau Protein and S-100B Levels in Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease.
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- Dementia & Geriatric Cognitive Disorders, 2005, v. 19, n. 5/6, p. 376, doi. 10.1159/000084708
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Results of Quinacrine Administration to Patients with Creutzfeldt-Jakob Disease.
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- Dementia & Geriatric Cognitive Disorders, 2004, v. 17, n. 3, p. 158, doi. 10.1159/000076350
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Alzheimer and Lewy Body Pathology or Creutzfeldt-Jakob Disease.
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- Collegium Antropologicum, 2014, v. 38, n. 2, p. 701
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- Article
Magnetic Resonance Spectroscopy and Measurement of Tau Epitopes of Autopsy Proven Sporadic Creutzfeldt-Jakob Disease in a Patient with Non-Specific Initial EEG, MRI and Negative 14-3-3 Immunoblot.
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- Collegium Antropologicum, 2008, v. 32, p. 199
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- Article
Wnikliwa obserwacja pacjenta i badanie elektroencefalograficzne mogą odegrać istotną rolę w rozpoznawaniu chorób rzadkich. Prezentacja przypadku choroby Creutzfeldta-Jakoba.
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- Current Neurology / Aktualno?ci Neurologiczne, 2021, v. 21, n. 2, p. 107, doi. 10.15557/AN.2021.0013
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- Article
Current activity of xenotransplantation in Japan.
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- Xenotransplantation, 2019, v. 26, n. 1, p. N.PAG, doi. 10.1111/xen.12487
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- Article
Apoptotic bodies in the cerebellum of Japanese patients with Creutzfeldt–Jakob disease.
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- Pathology International, 2001, v. 51, n. 3, p. 140, doi. 10.1046/j.1440-1827.2001.01181.x
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- Article
Cerebellar basket cells of Creutzfeldt–Jakob disease: Immunohistochemical and ultrastructural study.
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- Pathology International, 2000, v. 50, n. 4, p. 291, doi. 10.1046/j.1440-1827.2000.01038.x
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- Article
Argyrophilic grains in late-onset Creutzfeldt–Jakob diseased brain.
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- Pathology International, 1999, v. 49, n. 5, p. 369, doi. 10.1046/j.1440-1827.1999.00883.x
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- Article
Characterization of variably protease-sensitive prionopathy by capillary electrophoresis.
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- Scientific Reports, 2024, v. 12, n. 1, p. 1, doi. 10.1038/s41598-024-79217-1
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- Article
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
Screening of Anti-Prion Compounds Using the Protein Misfolding Cyclic Amplification Technology.
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- Biomolecules (2218-273X), 2024, v. 14, n. 9, p. 1113, doi. 10.3390/biom14091113
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- Article