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 3 (2007), Issue 2 (February)

1. vCJD and blood transfusion in the United Kingdom.
   Transfus Clin Biol, 13(5): 312-6. [Abstract] [Full-text]
2. Current strategies to prevent transmission of prions by human plasma derivatives.
   Transfus Clin Biol, 13(5): 320-8. [Abstract] [Full-text]
3. Supranuclear vertical gaze abnormalities in sporadic Creutzfeldt-Jakob disease.
   J Neurol Sci, 253(1): 69-72. [Abstract] [Full-text]
4. Recent developments in mucosal vaccines against prion diseases.
   Expert Rev Vaccines, 6(1): 75-85. [Abstract] [Full-text]
5. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
   J Neuropathol Exp Neurol, 66(2): 124-30. [Abstract] [Full-text]
6. Cells infected with scrapie and Creutzfeldt-Jakob disease agents produce intracellular 25-nm virus-like particles.
   Proc Natl Acad Sci U S A, 104(6): 1965-70. [Abstract] [Full-text]
7. The spread of prions through the body in naturally acquired transmissible spongiform encephalopathies.
   FEBS J, 274(3): 588-605. [Abstract] [Full-text]
8. Species-specificity of a Panel of Prion Protein Antibodies for the Immunohistochemical Study of Animal and Human Prion Diseases.
   J Comp Pathol, 136(1): 9-17. [Abstract] [Full-text]
9. A 25 nm virion is the likely cause of transmissible spongiform encephalopathies.
   J Cell Biochem, 100(4): 897-915. [Abstract] [Full-text]
10. Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease.
    J Gen Virol, 88: 1068-72. [Abstract] [Full-text]

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