Creutzfeldt-Jakob Disease Research Today is a free monthly online journal that collates and summarizes the latest research about Creutzfeldt-Jakob Disease, including details on mad cow disease, symptoms, causes, variants.

Volume 2 (2006), Issue 8 (August)

1. Tricyclic antidepressants, quinacrine and a novel, synthetic chimera thereof clear prions by destabilizing detergent-resistant membrane compartments.
   J Neurochem, 98(3): 748-59. [Abstract] [Full-text]
2. Iatrogenic Creutzfeldt-Jakob disease: the waning of an era.
   Neurology, 67(3): 389-93. [Abstract] [Full-text]
3. The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance.
   Neurology, 67(3): 531-3. [Abstract] [Full-text]
4. Clusterin expression in follicular dendritic cells associated with prion protein accumulation.
   J Pathol, 209(4): 484-91. [Abstract] [Full-text]
5. Methods to minimize the risks of Creutzfeldt-Jakob disease transmission by surgical procedures: where to set the standard?
   Clin Infect Dis, 43(6): 757-64. [Abstract] [Full-text]
6. Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium.
   Eur J Epidemiol, 21(6): 443-7. [Abstract] [Full-text]
7. CJD PrPsc removal by nanofiltration process: application to a therapeutic immunoglobulin solution (Lymphoglobuline).
   Biologicals, 34(3): 227-31. [Abstract] [Full-text]
8. Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJD.
   Brain, 129: 2288-96. [Abstract] [Full-text]
9. Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease.
   Brain, 129: 2278-87. [Abstract] [Full-text]
10. A systematic review of prion therapeutics in experimental models.
    Brain, 129: 2241-65. [Abstract] [Full-text]
11. CSF BACE1 activity is increased in CJD and Alzheimer disease other dementias.
    Neurology, 67(4): 710-2. [Abstract] [Full-text]
12. CSF tests in the differential diagnosis of Creutzfeldt-Jakob disease.
    Neurology, 67(4): 637-43. [Abstract] [Full-text]
13. Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.
    Brain, 129: 2297-317. [Abstract] [Full-text]
14. Classification of sporadic Creutzfeldt-Jakob disease revisited.
    Brain, 129: 2266-77. [Abstract] [Full-text]
15. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
    Nature, 442(7105): 916-9. [Abstract] [Full-text]
16. A novel copper-hydrogen peroxide formulation for prion decontamination.
    J Infect Dis, 194(6): 865-9. [Abstract] [Full-text]

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