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Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases.
- Published in:
- 2020
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- Publication type:
- journal article
Protective Effect of Val<sub>129</sub>-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.
- Published in:
- 2017
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- Publication type:
- journal article
Gerstmann-Sträussler-Scheinker disease with P102L prion protein gene mutation presenting with rapidly progressive clinical course.
- Published in:
- Clinical Neuropathology, 2014, v. 33, n. 5, p. 344, doi. 10.5414/NP300733
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- Publication type:
- Article
Panencephalopathic-type sporadic Creutzfeldt-Jakob disease with circumscribed spongy foci.
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- Clinical Neuropathology, 2014, v. 33, n. 2, p. 160, doi. 10.5414/NP300684
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- Publication type:
- Article
Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo.
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- Acta Neuropathologica Communications, 2021, v. 9, n. 1, p. 1, doi. 10.1186/s40478-021-01132-7
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- Publication type:
- Article
Molecular Barriers to Zoonotic Transmission of Prions.
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- Emerging Infectious Diseases, 2014, v. 20, n. 1, p. 88, doi. 10.3201/eid2001.130858
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- Publication type:
- Article
Medical Procedures and Risk for Sporadic Creutzfeldt-Jakob Disease, Japan, 1999-2008.
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- Emerging Infectious Diseases, 2009, v. 15, n. 2, p. 265, doi. 10.3201/eid1502.080749
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- Publication type:
- Article
Ophthalmic Surgery in Prion Diseases.
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- Emerging Infectious Diseases, 2007, v. 13, n. 1, p. 162, doi. 10.3201/eid1301.061004
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- Publication type:
- Article
Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.
- Published in:
- Nature Medicine, 2011, v. 17, n. 2, p. 175, doi. 10.1038/nm.2294
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- Publication type:
- Article
POSSIBLE HUMAN-TO-HUMAN TRANSMISSION OF CEREBRAL β-AMYLOIDOSIS VIA CADAVERIC DURA MATER GRAFTING.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1126, doi. 10.1016/j.jalz.2017.06.1636
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- Publication type:
- Article
COLOCALIZATION OF Aβ42 WITH PRPSC-PLAQUES IN THE BRAIN OF GERSTMANN-STRÄUSSLER-SCHEINKER DISEASE WITH THE P105L MUTATION.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P555, doi. 10.1016/j.jalz.2016.06.1083
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- Publication type:
- Article
A novel familial prion disease causing cognitive impairment, polyneuropathy and pan-autonomic involvement
- Published in:
- 2012
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- Publication type:
- Abstract
Human prion diseases in Japan: analysis of 1,552 patients in a prospective 11-year surveillance
- Published in:
- 2011
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- Publication type:
- Abstract
O1-04-03: Creutzfeldt-Jakob Disease (CJD) surveillance in Japan: Two distinct subtypes of CJD associated with cadaveric dura mater graft and the first Japanese case of variant CJD
- Published in:
- 2006
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- Publication type:
- Abstract
O1-04-03: Creutzfeldt-Jakob Disease (CJD) surveillance in Japan: Two distinct subtypes of CJD associated with cadaveric dura mater graft and the first Japanese case of variant CJD
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Descriptive Epidemiology of Prion Disease in Japan: 1999-2012.
- Published in:
- Journal of Epidemiology, 2015, v. 25, n. 1, p. 8, doi. 10.2188/jea.JE20140022
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- Publication type:
- Article
Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems.
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- Acta Neuropathologica Communications, 2014, v. 2, n. 1, p. 1, doi. 10.1186/2051-5960-2-32
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- Publication type:
- Article
An autopsy report of three kindred in a Gerstmann–Sträussler–Scheinker disease P105L family with a special reference to prion protein, tau, and beta‐amyloid.
- Published in:
- Brain & Behavior, 2018, v. 8, n. 10, p. N.PAG, doi. 10.1002/brb3.1117
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- Publication type:
- Article
Relationships between Clinicopathological Features and Cerebrospinal Fluid Biomarkers in Japanese Patients with Genetic Prion Diseases.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0060003
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- Publication type:
- Article
Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058786
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- Publication type:
- Article
Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution.
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- Journal of Neurology, 2007, v. 254, n. 11, p. 1509, doi. 10.1007/s00415-007-0540-9
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- Publication type:
- Article
Familial Creutzfeldt-Jakob Disease with a V180I Mutation: Comparative Analysis with Pathological Findings and Diffusion-Weighted Images.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2009, v. 28, n. 6, p. 550, doi. 10.1159/000254842
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- Publication type:
- Article
The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0706-6
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- Publication type:
- Article
PrP<sup>res</sup> deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD).
- Published in:
- 2018
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- Publication type:
- Letter
Neuroimaging-pathological correlations of [<sup>18</sup>F]THK5351 PET in progressive supranuclear palsy.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0556-7
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- Publication type:
- Article
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, p. 1, doi. 10.1186/s40478-017-0503-z
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- Publication type:
- Article
MIB1 staining index and scoring of histologic features in meningioma. Indicators for the prediction of biologic potential and postoperative management.
- Published in:
- 1994
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- Publication type:
- journal article
An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology.
- Published in:
- Neuropathology, 2010, v. 30, n. 2, p. 159, doi. 10.1111/j.1440-1789.2009.01048.x
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- Publication type:
- 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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- Publication type:
- Article
An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein.
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- Neuropathology, 2009, v. 29, n. 6, p. 727, doi. 10.1111/j.1440-1789.2009.01016.x
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- Publication type:
- Article
Creutzfeldt-Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum.
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- Neuropathology, 2009, v. 29, n. 6, p. 735, doi. 10.1111/j.1440-1789.2009.01019.x
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- Publication type:
- Article
The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures.
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- Neuropathology, 2009, v. 29, n. 5, p. 625, doi. 10.1111/j.1440-1789.2009.01023.x
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- Publication type:
- Article
A traceback phenomenon can reveal the origin of prion infection.
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- Neuropathology, 2009, v. 29, n. 5, p. 619, doi. 10.1111/j.1440-1789.2008.00973.x
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- Publication type:
- Article
Dura mater graft-associated Creutzfeldt-Jakob disease in Japan: Clinicopathological and molecular characterization of the two distinct subtypes.
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- Neuropathology, 2009, v. 29, n. 5, p. 609, doi. 10.1111/j.1440-1789.2008.00987.x
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- Publication type:
- Article
Coexistence of Creutzfeldt-Jakob disease, Lewy body disease, and Alzheimer's disease pathology: An autopsy case showing typical clinical features of Creutzfeldt-Jakob disease.
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- Neuropathology, 2009, v. 29, n. 4, p. 454, doi. 10.1111/j.1440-1789.2008.00964.x
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- Publication type:
- Article
MM2-cortical-type sporadic Creutzfeldt-Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course.
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- Neuropathology, 2008, v. 28, n. 6, p. 645, doi. 10.1111/j.1440-1789.2008.00904.x
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- Publication type:
- Article
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
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- Neuropathology, 2008, v. 28, n. 3, p. 326, doi. 10.1111/j.1440-1789.2007.00854.x
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- Publication type:
- Article
Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease.
- Published in:
- Neuropathology, 2008, v. 28, n. 1, p. 51, doi. 10.1111/j.1440-1789.2007.00847.x
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- Publication type:
- Article
Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob disease.
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- Neuropathology, 2007, v. 27, n. 4, p. 314, doi. 10.1111/j.1440-1789.2007.00781.x
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- Publication type:
- Article
Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease.
- Published in:
- Neuropathology, 2007, v. 27, n. 5, p. 434, doi. 10.1111/j.1440-1789.2007.00812.x
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- Publication type:
- Article
Autopsy case of sporadic Creutzfeldt–Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement.
- Published in:
- Neuropathology, 2006, v. 26, n. 6, p. 550, doi. 10.1111/j.1440-1789.2006.00723.x
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- Publication type:
- Article
Severe cortical involvement in MV2 Creutzfeldt–Jakob disease: An autopsy case report.
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- Neuropathology, 2006, v. 26, n. 5, p. 433, doi. 10.1111/j.1440-1789.2006.00705.x
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- Publication type:
- Article
Autopsy case of Creutzfeldt–Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum.
- Published in:
- Neuropathology, 2006, v. 26, n. 4, p. 313, doi. 10.1111/j.1440-1789.2006.00683.x
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- Publication type:
- Article
Increased asymmetric pulvinar magnetic resonance imaging signals in Creutzfeldt–Jakob disease with florid plaques following a cadaveric dura mater graft.
- Published in:
- Neuropathology, 2006, v. 26, n. 1, p. 82, doi. 10.1111/j.1440-1789.2006.00638.x
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- Publication type:
- Article
Sporadic fatal insomnia with spongiform degeneration in the thalamus and widespread PrP<sup>Sc</sup> deposits in the brain.
- Published in:
- Neuropathology, 2005, v. 25, n. 2, p. 144, doi. 10.1111/j.1440-1789.2005.00608.x
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- Publication type:
- Article
Creutzfeldt–Jakob disease with florid plaques after cadaveric dura mater graft.
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- Neuropathology, 2003, v. 23, n. 2, p. 136, doi. 10.1046/j.1440-1789.2003.00489.x
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- Publication type:
- Article
Creutzfeldt--Jakob disease.
- Published in:
- Neuropathology, 2000, v. 20, p. S52, doi. 10.1046/j.1440-1789.2000.00308.x
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- Publication type:
- Article
Human Prion Diseases: Creutzfeldt-Jakob Disease, Gerstmann-Sträussler Syndrome, and Unknown Dementia.
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- Neuropathology, 1993, v. 13, n. 2, p. 93, doi. 10.1111/j.1440-1789.1993.tb00218.x
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- Publication type:
- Article
Reply: Prion protein gene M232R variation is probably an uncommon polymorphism rather than a pathogenic mutation.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 2, p. e210, doi. 10.1093/brain/awr295
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- Publication type:
- Article
Prospective 10-year surveillance of human prion diseases in Japan.
- Published in:
- Brain: A Journal of Neurology, 2010, v. 133, n. 10, p. 3043, doi. 10.1093/brain/awq216
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- Publication type:
- Article