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 5 (May)

1. Follow-up investigations of tau protein and S-100B levels in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.
   Dement Geriatr Cogn Disord, 19(5): 376-82. [Abstract] [Full-text]
2. Presymptomatic signs in healthy CJD mutation carriers.
   Dement Geriatr Cogn Disord, 19(5): 246-55. [Abstract] [Full-text]
3. Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patients.
   Neurology, 64(9): 1618-20. [Abstract] [Full-text]
4. High incidence of genetic human transmissible spongiform encephalopathies in Italy.
   Neurology, 64(9): 1592-7. [Abstract] [Full-text]
5. Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada.
   Neurology, 64(9): 1586-91. [Abstract] [Full-text]
6. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
   Acta Neuropathol (Berl), 109(4): 443-8. [Abstract] [Full-text]
7. The "pulvinar sign" in a case of paraneoplastic limbic encephalitis associated with non-Hodgkin's lymphoma.
   J Neurol Neurosurg Psychiatry, 76(6): 882-4. [Abstract] [Full-text]
8. Ancestral origins of the prion protein gene D178N mutation in the Basque Country.
   Hum Genet, 117(1): 61-9. [Abstract] [Full-text]
9. Cerebroventricular infusion of pentosan polysulphate in human variant Creutzfeldt-Jakob disease.
   J Infect, 50(5): 394-6. [Abstract] [Full-text]
10. Evaluation of urinary PrPSc as a diagnostic test for sporadic, variant, and familial CJD.
    Neurology, 64(10): 1794-6. [Abstract] [Full-text]

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