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 1 (2005), Issue 4 (April)

1. Sporadic Creutzfeldt-Jakob disease: a comparison of pathological findings and diffusion weighted imaging.
   J Neurol, 252(3): 338-42. [Abstract] [Full-text]
2. Lay and expert perceptions of zoonotic risks: understanding conflicting perspectives in the light of moral theory.
   Int J Food Microbiol, 99(3): 245-55. [Abstract] [Full-text]
3. Annulling a dangerous liaison: vaccination strategies against AIDS and tuberculosis.
   Nat Med, 11(4): S33-44. [Abstract] [Full-text]
4. Variation in concentration of prion protein in the peripheral blood of patients with variant and sporadic Creutzfeldt-Jakob disease detected by dissociation enhanced lanthanide fluoroimmunoassay and flow cytometry.
   Transfusion, 45(4): 504-13. [Abstract] [Full-text]
5. Human prion diseases: molecular and clinical aspects.
   Arch Neurol, 62(4): 545-52. [Abstract] [Full-text]
6. Transmission barriers for bovine, ovine, and human prions in transgenic mice.
   J Virol, 79(9): 5259-71. [Abstract] [Full-text]
7. Periodic motor cortical excitability changes associated with PSDs of EEG in Creutzfeldt-Jakob disease (CJD).
   Clin Neurophysiol, 116(5): 1222-6. [Abstract] [Full-text]
8. Gene SNPs and mutations in clinical genetic testing: haplotype-based testing and analysis.
   Mutat Res, 573(1): 195-204. [Abstract] [Full-text]
9. Characterization of light chain immunoglobulin in urine from animals and humans infected with prion diseases.
   J Neuroimmunol, 162(1): 12-8. [Abstract] [Full-text]
10. Activation of human microglia by fibrillar prion protein-related peptides is enhanced by amyloid-associated factors SAP and C1q.
    Neurobiol Dis, 19(1): 273-82. [Abstract] [Full-text]
11. Synthetic prions generated in vitro are similar to a newly identified subpopulation of PrPSc from sporadic Creutzfeldt-Jakob Disease.
    Protein Sci, 14(5): 1222-32. [Abstract] [Full-text]
12. Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.
    J Neurol Sci, 232(1): 45-9. [Abstract] [Full-text]
13. Prion protein glycosylation.
    J Neurochem, 93(4): 793-801. [Abstract] [Full-text]

© 2005-2008 Creutzfeldt-Jakob Disease Research Today. All Rights Reserved.