Works matching Variant Creutzfeldt-Jakob disease
Results: 678
Probable variant Creutzfeldt-Jakob disease in Asia: A case report from Taiwan and review of two prior cases.
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- Psychiatry & Clinical Neurosciences, 2010, v. 64, n. 6, p. 652, doi. 10.1111/j.1440-1819.2010.02151.x
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- Article
Batch recall of French plasma-derived products due to variant Creutzfeldt-Jakob disease risk: the psychological impact on haemophilic patients, changes in their therapeutic demands and behaviour and ethical considerations.
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- Haemophilia, 2015, v. 21, n. 1, p. 27, doi. 10.1111/hae.12515
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- Article
Risk reduction strategies for variant Creutzfeldt–Jakob disease transmission by UK plasma products and their impact on patients with inherited bleeding disorders.
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- Haemophilia, 2010, v. 16, n. 2, p. 305, doi. 10.1111/j.1365-2516.2010.02220.x
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- Article
Clinical implications of emerging pathogens in haemophilia: the variant Creutzfeldt–Jakob disease experience.
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- Haemophilia, 2006, v. 12, p. 16, doi. 10.1111/j.1365-2516.2006.01196.x
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- Article
Variant Creutzfeldt–Jakob disease: risk of transmission by blood transfusion and blood therapies.
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- Haemophilia, 2006, v. 12, p. 8, doi. 10.1111/j.1365-2516.2006.01195.x
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- Article
The first Japanese patient with variant Creutzfeldt-Jakob disease (vCJD).
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- Neuropathology, 2009, v. 29, n. 6, p. 713, doi. 10.1111/j.1440-1789.2009.01006.x
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- Article
An application of hidden Markov models to the French variant Creutzfeldt-Jakob disease epidemic.
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- Journal of the Royal Statistical Society: Series C (Applied Statistics), 2010, v. 59, n. 5, p. 839, doi. 10.1111/j.1467-9876.2010.00714.x
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- Article
Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.
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- 2019
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- journal article
A case cluster of variant Creutzfeldt-Jakob disease linked to the Kingdom of Saudi Arabia.
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- Brain: A Journal of Neurology, 2016, v. 139, n. 10, p. 2609, doi. 10.1093/brain/aww206
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- Article
Ultrastructural study of florid plaques in variant Creutzfeldt–Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt–Jakob disease and Gerstmann–Sträussler–Scheinker disease.
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- Neuropathology & Applied Neurobiology, 2009, v. 35, n. 1, p. 46, doi. 10.1111/j.1365-2990.2008.00959.x
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- Article
A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt–Jakob disease (vCJD).
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- Neuropathology & Applied Neurobiology, 2009, v. 35, n. 1, p. 36, doi. 10.1111/j.1365-2990.2008.00979.x
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- Article
No Adaptation of the Prion Strain in a Heterozygous Case of Variant Creutzfeldt-Jakob Disease.
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- 2020
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- journal article
Distribution and Quantitative Estimates of Variant Creutzfeldt-Jakob Disease Prions in Tissues of Clinical and Asymptomatic Patients.
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- 2017
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- journal article
Variant Creutzfeldt–Jakob disease: costs borne by families.
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- Health & Social Care in the Community, 2002, v. 10, n. 2, p. 91, doi. 10.1046/j.1365-2524.2002.00346.x
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- Article
Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease.
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- Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 1139, doi. 10.1093/brain/awt032
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- Article
Survival and Re-Operation Rates after Neurosurgical Procedures in Scotland: Implications for Targeted Surveillance of Sub-Clinical Variant Creutzfeldt-Jakob Disease.
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- Neuroepidemiology, 2009, v. 33, n. 1, p. 1, doi. 10.1159/000209281
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- Article
Does Poor Dental Health Have a Role in the Emergence of Variant Creutzfeldt Jakob Disease in the United Kingdom?
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- Dental Hypotheses, 2011, v. 2, p. 74, doi. 10.5436/j.dehy.2011.2.00030
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- Article
Neuropathological changes in striate and extrastriate visual cortex in variant Creutzfeldt-Jakob disease (vCJD).
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- Clinical Ophthalmology, 2007, v. 1, n. 2, p. 119
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- Article
Size frequency distribution of prion protein (PrP) aggregates in variant Creutzfeldt-Jakob disease (vCJD).
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- Journal of Neural Transmission, 2005, v. 112, n. 11, p. 1565, doi. 10.1007/s00702-005-0296-2
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- Article
Spatial correlations between the vacuolation, prion protein deposition and surviving neurons in variant Creutzfeldt-Jakob Disease (vCJD).
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- Journal of Neural Transmission, 2003, v. 110, n. 11, p. 1303, doi. 10.1007/s00702-003-0039-1
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- Article
Dealing with the uncertain risk of variant Creutzfeldt- Jakob disease transmission by coagulation replacement products.
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- British Journal of Haematology, 2012, v. 158, n. 4, p. 442, doi. 10.1111/j.1365-2141.2012.09201.x
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- Article
Smallde novoduplication in the repeat region of the TATA-box-binding protein gene manifest with a phenotype similar to variant Creutzfeldt-Jakob disease.
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- Clinical Genetics, 2004, v. 66, n. 6, p. 496, doi. 10.1111/j.1399-0004.2004.00356.x
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- Article
Variant Creutzfeldt-Jakob disease: an unfolding epidemic of misfolded proteins.
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- 2002
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- journal article
The spatial patterns of prion protein deposits in cases of variant Creutzfeldt-Jakob disease.
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- Acta Neuropathologica, 2002, v. 104, n. 6, p. 665, doi. 10.1007/s00401-002-0598-5
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- Article
Electron microsocopy of brain amyloid plaques from a patient with new variant Creutzfeldt-Jakob disease.
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- Acta Neuropathologica, 2000, v. 99, n. 6, p. 637, doi. 10.1007/s004010051174
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- Article
Size frequency distributions of the florid prion protein aggregates in variant Creutzfeldt-Jakob disease follow a power-law function.
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- 2006
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- journal article
Comparison of the neuropathological characteristics of bovine spongiform encephalopathy (BSE) and variant Creutzfeldt–Jakob disease (vCJD) in mice.
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- Neuropathology & Applied Neurobiology, 2003, v. 29, n. 3, p. 262, doi. 10.1046/j.1365-2990.2003.00462.x
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- Article
Quantification of vacuolation (‘spongiform change’), surviving neurones and prion protein deposition in eleven cases of variant Creutzfeldt–Jakob disease.
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- Neuropathology & Applied Neurobiology, 2002, v. 28, n. 2, p. 129, doi. 10.1046/j.1365-2990.2002.00386.x
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- Article
Preclinical Detection of Prions in Blood of Nonhuman Primates Infected with Variant Creutzfeldt-Jakob Disease.
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- 2020
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- journal article
Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification.
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- 2018
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- journal article
Protective Effect of Val<sub>129</sub>-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.
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- 2017
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- journal article
Has the frequency of ABO RhD blood groups in Australian blood donors changed as a result of the removal of the variant Creutzfeldt–Jakob disease‐based deferral?
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- Vox Sanguinis, 2024, v. 119, n. 6, p. 619, doi. 10.1111/vox.13614
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- Article
Risk of variant Creutzfeldt–Jakob disease transmission by blood transfusion in Australia.
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- Vox Sanguinis, 2022, v. 117, n. 8, p. 1016, doi. 10.1111/vox.13290
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- Article
Risks of transmission of variant Creutzfeldt-Jakob disease by blood transfusion.
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- Folia Neuropathologica, 2005, v. 43, n. 4, p. 271
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- Article
Diagnostic accuracy of diffusion-weighted imaging in variant Creutzfeldt–Jakob disease.
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- Neuroradiology, 2023, v. 65, n. 12, p. 1715, doi. 10.1007/s00234-023-03230-w
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Sensory features of variant Creutzfeldt-Jakob disease.
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- Journal of Neurology, 2002, v. 249, n. 6, p. 706, doi. 10.1007/s00415-002-0696-2
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- Article
Variant Creutzfeldt–Jakob disease: first two indigenous cases in Republic of Ireland. Case report and perspective.
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- European Journal of Neurology, 2007, v. 14, n. 4, p. 467, doi. 10.1111/j.1468-1331.2007.01643.x
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- Article
Heidenhain variant of Creutzfeldt–Jakob disease resembles dementia with Lewy bodies.
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- Psychogeriatrics, 2021, v. 21, n. 1, p. 121, doi. 10.1111/psyg.12640
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- Article
Universal leucodepletion to reduce the risk of transmission of new-variant creutzfeldt–jakob disease.
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- British Journal of Haematology, 2000, v. 110, n. 1, p. 234, doi. 10.1046/j.1365-2141.2000.02072.x
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- Article
Heidenhain variant of Creutzfeldt-Jakob disease in a patient who had bovine bioprosthetic valve implantation.
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- 2016
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- journal article
Unusual Dopaminergic Depletion in Variant Creutzfeldt-Jakob Disease with Early and Rapid Cognitive Decline.
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- European Neurology, 2011, v. 65, n. 6, p. 368, doi. 10.1159/000328670
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- Article
Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: U.K. cases 1991-2002.
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- 2004
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- Journal Article
Prion protein heterogeneity in sporadic but not variant CreutzfeldtJakob disease: U.K. cases 19912002.
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- Annals of Neurology, 2004, v. 55, n. 6, p. 851
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- Article
Clearance of variant Creutzfeldt-Jakob disease prions in vivo by the Hsp70 disaggregase system.
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- 2022
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- journal article
RNA integrity in post mortem human variant Creutzfeldt-Jakob disease (vCJD) and control brain tissue.
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- Neuropathology & Applied Neurobiology, 2011, v. 37, n. 6, p. 633, doi. 10.1111/j.1365-2990.2011.01162.x
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- Article
Reduplicative paramnesia as an atypical form of presentation of a Heidenhain variant of Creutzfeldt-Jakob disease: A case report.
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- Journal of the International Neuropsychological Society, 2023, v. 29, n. 6, p. 615, doi. 10.1017/S1355617722000583
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- Article
Correlation of Polydispersed Prion Protein and Characteristic Pathology in the Thalamus in Variant Creutzfeldt-Jakob Disease: Implication of Small Oligomeric Species.
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- Brain Pathology, 2011, v. 21, n. 3, p. 298, doi. 10.1111/j.1750-3639.2010.00446.x
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- Article
Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.
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- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-91
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- Article
Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.
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- 2013
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- journal article
The Heidenhain variant of Creutzfeldt–Jakob disease.
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- 2018
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- Case Study