Recent Publications on Jakob-Creutzfeldt Disease Creutzfeldt-Jakob Disease: |  |
[Hashimoto encephalopathy - a difficult differential diagnosis.]
INTRODUCTION: Hashimoto encephalopathy is a rare disease that is...
Direct Link | 4th October, 2008
| Evangelisches Krankenhaus Konigin Elisabeth Herzberge, Abt. fur
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Wernicke's encephalopathy mimicking variant Creutzfeldt-Jakob disease.
A 45-year-old man from tropical Australia was admitted with subacute...
Direct Link | 3rd October, 2008
| Department Neurology, Cairns Base Hospital and James Cook University,
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Brain biopsy in patients with suspected Creutzfeldt-Jakob disease.
Object Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative...
Direct Link | 2nd October, 2008
| 1 Departments of Neurology,, 2 Neuroradiology, and, 3 Neuropathology,
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| Policy to reduce the risk costs the environment dear.
| 30th September, 2008
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Cerebrospinal fluid-optimized two-dimensional difference gel electrophoresis (2-D DIGE) facilitates the differential diagnosis of Creutzfeldt-Jakob disease.
So far only the detection of 14-3-3 proteins in cerebrospinal fluid (CSF)...
Direct Link | 25th September, 2008
| Department of Neurodegeneration and Restorative Research, Center of
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MRI of sporadic Creutzfeldt-Jakob disease.
The key MRI findings in five cases of sporadic Creutzfeldt-Jakob disease...
Direct Link | 25th September, 2008
| Regional Imaging Border, Albury Wodonga Private Hospital, Albury, New
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Relationship between clinical course and Diffusion-weighted MRI findings in sporadic Creutzfeldt-Jakob Disease.
The aim of this study was to investigate the relationship between clinical...
Direct Link | 24th September, 2008
| Department of Neurology Kyung Hee Medical Center, Kyung Hee University
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Association of a null allele of SPRN with variant Creutzfeldt-Jakob Disease.
Despite clear evidence from mouse linkage studies of multiple genetic loci...
Direct Link | 23rd September, 2008
| MRC Prion Unit, United Kingdom.
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| Normalization of 14-3-3 in CJD.
| 18th September, 2008
| Department of Neurology, University of Leuven, Belgium.
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Cellular factors important for the de novo formation of yeast prions.
Prions represent an unusual structural form of a protein that is...
Direct Link | 17th September, 2008
| Protein Science Group, Department of Biosciences, University of Kent,
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Quantitative recovery of scrapie agent with minimal protein from highly infectious cultures.
There are few reports on the isolation, quantitative recovery, and...
Direct Link | 16th September, 2008
| Section of Neuropathology, Yale Medical School, New Haven, Connecticut
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BSE case associated with prion protein gene mutation.
Bovine spongiform encephalopathy (BSE) is a transmissible spongiform...
Direct Link | 13th September, 2008
| National Animal Disease Center, United States Department of Agriculture,
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[Creutzfeldt-Jakob disease in patients before and after 80 years of age.]
The frequency of sporadic CJD is maximum in the 70 to 79 years age group...
Direct Link | 13th September, 2008
| Inserm U708, Paris.
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The identification of disease-induced biomarkers in the urine of BSE infected cattle.
ABSTRACT: BACKGROUND: The bovine spongiform encephalopathy (BSE) epidemic...
Direct Link | 9th September, 2008
| Prion Diseases Program, Public Health Agency of Canada, Winnipeg, R3E 3P6,
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| Surveillance of Creutzfeldt-Jakob disease in Australia: 2008.
| 5th September, 2008
| Australiian National Creutzfeldt-Jakob Disease Registry, Department of
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