Works matching DE "CREUTZFELDT-Jakob disease"
Results: 2048
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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Confused About Dementias.
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- ISNA Bulletin, 2018, v. 44, n. 4, p. 11
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Navigating the ClpB channel to solution.
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- Nature Structural & Molecular Biology, 2005, v. 12, n. 1, p. 4, doi. 10.1038/nsmb0105-4
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The human prion disease hypothesis does not justify the origin of bovine spongiform encephalopathy.
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- Journal of Postgraduate Medicine, 2006, v. 52, n. 3, p. 223
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Clinical characteristics of Creutzfeldt-Jakob disease in Mexico: A retrospective analysis.
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- Revista Mexicana de Neurociencia, 2020, v. 21, n. 6, p. 228, doi. 10.24875/RMN.20000099
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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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A sporadic case of Creutzfeldt- Jakob disease showing unilateral hemispheric involvement on magnetic resonance imaging.
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- Psychogeriatrics, 2017, v. 17, n. 6, p. 517, doi. 10.1111/psyg.12272
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Probable sporadic Creutzfeldt- Jakob disease mimicking a catatonic depression in an elderly adult.
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- Psychogeriatrics, 2017, v. 17, n. 6, p. 524, doi. 10.1111/psyg.12264
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Creutzfeldt-Jakob disease.
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- Psychogeriatrics, 2011, v. 11, n. 2, p. 119, doi. 10.1111/j.1479-8301.2011.00361.x
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A case of dementia with Lewy bodies that temporarily showed symptoms similar to Creutzfeldt-Jakob disease.
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- Psychogeriatrics, 2010, v. 10, n. 4, p. 201, doi. 10.1111/j.1479-8301.2010.00336.x
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Early symptoms of Creutzfeldt-Jacob disease mimicking alcohol-related disorder.
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- Psychogeriatrics, 2009, v. 9, n. 3, p. 143, doi. 10.1111/j.1479-8301.2009.00275.x
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Right parietal lobe syndrome as a clinical variant of Creutzfeldt-Jakob disease.
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- Psychogeriatrics, 2006, v. 6, n. 2, p. 74, doi. 10.1111/j.1479-8301.2006.00154.x
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Positive Selection in Prion Protein.
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- Journal of Molecular Evolution, 2009, v. 68, n. 3, p. 205, doi. 10.1007/s00239-008-9176-3
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Prion susceptibility and protective alleles exhibit marked geographic differences (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #628 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/628.pdf)
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- Human Mutation, 2003, v. 22, n. 1, p. 104, doi. 10.1002/humu.9157
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Prion susceptibility and protective alleles exhibit marked geographic differencesCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #628 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/628.pdf.
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- Human Mutation, 2003, v. 22, n. 1, p. 104, doi. 10.1002/humu.9157
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Rapid echoplanar diffusion imaging in a case of variant Creutzfeldt-Jakob disease; where speed is of the essence.
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- Neuroradiology, 2003, v. 45, n. 8, p. 528, doi. 10.1007/s00234-003-1050-9
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Extensive cortical damage in a case of Creutzfeldt-Jacob disease: clinicoradiological correlations.
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- Neuroradiology, 2003, v. 45, n. 5, p. 304, doi. 10.1007/s00234-003-0939-7
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Magnetic resonance diffusion-weighted images in Creutzfeldt-Jakob disease: case report.
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- Neuroradiology, 2003, v. 45, n. 1, p. 50, doi. 10.1007/s00234-002-0892-x
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Multitracer study with positron emission tomography in Creutzfeldt-Jakob disease.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2003, v. 30, n. 1, p. 85, doi. 10.1007/s00259-002-1008-x
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The role of stress and anxiety in the onset of familial Creutzfeldt-Jakob Disease (CJD): Review.
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- Stress: The International Journal on the Biology of Stress, 2009, v. 12, n. 5, p. 371, doi. 10.1080/10253890802508520
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Unsuccessful transmissions of atypical genetic Creutzfeldt–Jakob disease (PRNP p.T183A-129M) in transgenic mice.
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- 2024
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- Letter
Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease.
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- Acta Neuropathologica, 2024, v. 148, n. 1, p. 1, doi. 10.1007/s00401-024-02774-2
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Correction: A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 167, doi. 10.1007/s00401-023-02592-y
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A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques.
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- Acta Neuropathologica, 2023, v. 146, n. 1, p. 121, doi. 10.1007/s00401-023-02581-1
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A point mutation in GPI-attachment signal peptide accelerates the development of prion disease.
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- Acta Neuropathologica, 2023, v. 145, n. 5, p. 637, doi. 10.1007/s00401-023-02553-5
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DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 785, doi. 10.1007/s00401-022-02481-w
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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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Strain diversity in neurodegenerative disease: an argument for a personalized medicine approach to diagnosis and treatment.
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- 2021
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- Editorial
Environmental and host factors that contribute to prion strain evolution.
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- Acta Neuropathologica, 2021, v. 142, n. 1, p. 5, doi. 10.1007/s00401-021-02310-6
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Tau strains shape disease.
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- Acta Neuropathologica, 2021, v. 142, n. 1, p. 57, doi. 10.1007/s00401-021-02301-7
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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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Wide distribution of prion infectivity in the peripheral tissues of vCJD and sCJD patients.
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- Acta Neuropathologica, 2021, v. 141, n. 3, p. 383, doi. 10.1007/s00401-021-02270-x
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Lewy pathology of the esophagus correlates with the progression of Lewy body disease: a Japanese cohort study of autopsy cases.
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- Acta Neuropathologica, 2021, v. 141, n. 1, p. 25, doi. 10.1007/s00401-020-02233-8
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Direct neural transmission of vCJD/BSE in macaque after finger incision.
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- Acta Neuropathologica, 2021, v. 141, n. 1, p. 119, doi. 10.1007/s00401-020-02231-w
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Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease.
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- Acta Neuropathologica, 2020, v. 140, n. 6, p. 863, doi. 10.1007/s00401-020-02224-9
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The coarse-grained plaque: a divergent Aβ plaque-type in early-onset Alzheimer's disease.
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- Acta Neuropathologica, 2020, v. 140, n. 6, p. 811, doi. 10.1007/s00401-020-02198-8
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Distinct clinicopathologic clusters of persons with TDP-43 proteinopathy.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 659, doi. 10.1007/s00401-020-02211-0
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Prion propagation estimated from brain diffusion MRI is subtype dependent in sporadic Creutzfeldt–Jakob disease.
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- Acta Neuropathologica, 2020, v. 140, n. 2, p. 169, doi. 10.1007/s00401-020-02168-0
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Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic.
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- Acta Neuropathologica, 2020, v. 139, n. 6, p. 965, doi. 10.1007/s00401-020-02153-7
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Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions.
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- Acta Neuropathologica, 2020, v. 139, n. 3, p. 527, doi. 10.1007/s00401-019-02085-x
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Calling α-synuclein a prion is scientifically justifiable.
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- 2019
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- Letter
Alpha-synuclein: prion or prion-like?
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- 2019
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- Letter
Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies.
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- Acta Neuropathologica, 2019, v. 137, n. 3, p. 363, doi. 10.1007/s00401-018-1941-9
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Fatal Aβ cerebral amyloid angiopathy 4 decades after a dural graft at the age of 2 years.
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- 2018
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- Letter to the Editor
Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK.
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- Acta Neuropathologica, 2017, v. 134, n. 2, p. 221, doi. 10.1007/s00401-017-1703-0
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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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UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches.
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- Acta Neuropathologica, 2017, v. 133, n. 4, p. 579, doi. 10.1007/s00401-016-1638-x
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Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 21, doi. 10.1007/s00401-010-0760-4
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Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 39, doi. 10.1007/s00401-010-0713-y
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The application of in vitro cell-free conversion systems to human prion diseases.
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- Acta Neuropathologica, 2011, v. 121, n. 1, p. 135, doi. 10.1007/s00401-010-0708-8
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