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Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases.
- Published in:
- 2020
- By:
- 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
An autopsy case of variably protease‐sensitive prionopathy with Met/Met homogeneity at codon 129.
- Published in:
- Neuropathology, 2023, v. 43, n. 6, p. 486, doi. 10.1111/neup.12911
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- Publication type:
- Article
V180I genetic Creutzfeldt‐Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain.
- Published in:
- Neuropathology, 2023, v. 43, n. 6, p. 479, doi. 10.1111/neup.12908
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- Publication type:
- Article
An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings.
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- Neuropathology, 2022, v. 42, n. 3, p. 245, doi. 10.1111/neup.12804
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- Publication type:
- Article
Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case.
- Published in:
- Neuropathology, 2021, v. 41, n. 3, p. 206, doi. 10.1111/neup.12722
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- Publication type:
- Article
Identification of intracerebral hemorrhage in the early‐phase of MM1+2C‐type sporadic Creutzfeldt–Jakob disease: A case report.
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- Neuropathology, 2020, v. 40, n. 4, p. 399, doi. 10.1111/neup.12658
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- Publication type:
- Article
Autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease with spongiform changes of the cerebral cortex.
- Published in:
- Neuropathology, 2019, v. 39, n. 6, p. 452, doi. 10.1111/neup.12595
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- Publication type:
- Article
Autopsied case of sporadic Creutzfeldt–Jakob disease classified as MM1+2C‐type.
- Published in:
- Neuropathology, 2019, v. 39, n. 3, p. 240, doi. 10.1111/neup.12557
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- Publication type:
- Article
Autopsy case of V180I genetic Creutzfeldt‐Jakob disease presenting with early disease pathology.
- Published in:
- 2018
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- Publication type:
- Case Study
Autopsied case of non‐plaque‐type dura mater graft‐associated Creutzfeldt‐Jakob disease presenting with extensive amyloid‐β deposition.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
An autopsy case of Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction.
- Published in:
- Neuropathology, 2017, v. 37, n. 6, p. 575, doi. 10.1111/neup.12399
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- Publication type:
- Article
MM1-type sporadic Creutzfeldt-Jakob disease with 1-month total disease duration and early pathologic indicators.
- Published in:
- Neuropathology, 2017, v. 37, n. 5, p. 420, doi. 10.1111/neup.12379
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- Publication type:
- Article
An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.
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- Neuropathology, 2017, v. 37, n. 3, p. 241, doi. 10.1111/neup.12350
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- Publication type:
- Article
An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.
- Published in:
- Neuropathology, 2017, v. 37, n. 1, p. 78, doi. 10.1111/neup.12327
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- Publication type:
- Article
Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
- Published in:
- Neuropathology, 2016, v. 36, n. 3, p. 305, doi. 10.1111/neup.12270
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- Publication type:
- Article
Extensive cortical spongiform changes with cerebellar small amyloid plaques: The clinicopathological case of MV2K+ C subtype in Creutzfeldt- Jakob disease.
- Published in:
- Neuropathology, 2014, v. 34, n. 6, p. 541, doi. 10.1111/neup.12133
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- Publication type:
- Article
An autopsied case of Creutzfeldt- Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.
- Published in:
- Neuropathology, 2013, v. 33, n. 5, p. 568, doi. 10.1111/neup.12013
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- Publication type:
- Article
An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease.
- Published in:
- Neuropathology, 2011, v. 31, n. 5, p. 523, doi. 10.1111/j.1440-1789.2010.01181.x
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- Publication type:
- Article
An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type.
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- Neuropathology, 2011, v. 31, n. 5, p. 540, doi. 10.1111/j.1440-1789.2010.01192.x
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- Publication type:
- 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
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 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
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.
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- Neuropathology, 2008, v. 28, n. 1, p. 51, doi. 10.1111/j.1440-1789.2007.00847.x
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- Publication type:
- Article
Pyramidal tract degeneration in sporadic Creutzfeldt-Jakob disease.
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- Neuropathology, 2007, v. 27, n. 5, p. 434, doi. 10.1111/j.1440-1789.2007.00812.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
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.
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- Neuropathology, 1993, v. 13, n. 2, p. 93, doi. 10.1111/j.1440-1789.1993.tb00218.x
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- Publication type:
- Article
Creutzfeldt-Jakob disease with Alzheimer pathology, presenting with status epilepticus following repeated partial seizures: a case report and literature review.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Molecular Barriers to Zoonotic Transmission of Prions.
- Published in:
- 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.
- Published in:
- 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.
- Published in:
- Emerging Infectious Diseases, 2007, v. 13, n. 1, p. 162, doi. 10.3201/eid1301.061004
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- Publication type:
- Article
Critical Significance of the Region between Helix 1 and 2 for Efficient Dominant-Negative Inhibition by Conversion-Incompetent Prion Protein.
- Published in:
- PLoS Pathogens, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.ppat.1003466
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- Publication type:
- Article
Correction to: In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP<sup>V180I</sup> Mutation.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP<sup>V180I</sup> Mutation.
- Published in:
- Molecular Neurobiology, 2019, v. 56, n. 8, p. 5456, doi. 10.1007/s12035-018-1459-0
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- Publication type:
- Article
A point mutation in GPI-attachment signal peptide accelerates the development of prion disease.
- Published in:
- Acta Neuropathologica, 2023, v. 145, n. 5, p. 637, doi. 10.1007/s00401-023-02553-5
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- Publication type:
- Article
Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy.
- Published in:
- 2016
- By:
- Publication type:
- Letter