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 11 (November)

1. Variant Creutzfeldt-Jakob disease transmission by plasma products: assessing and communicating risk in an era of scientific uncertainty.
   Vox Sang, 89(4): 186-92. [Abstract] [Full-text]
2. Ethical considerations in presymptomatic testing for variant CJD.
   J Med Ethics, 31(11): 625-30. [Abstract] [Full-text]
3. Risk perception of the "mad cow disease" in France: determinants and consequences.
   Risk Anal, 25(4): 813-26. [Abstract] [Full-text]
4. Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be responsible for differences in bovine spongiform encephalopathy susceptibility.
   J Biol Chem, 280(45): 37408-14. [Abstract] [Full-text]
5. Safe method for isolation of prion protein and diagnosis of Creutzfeldt-Jakob disease.
   J Virol Methods, 130(1): 133-9. [Abstract] [Full-text]
6. Phenotypic variability in human prion diseases.
   Neuropathol Appl Neurobiol, 31(6): 565-79. [Abstract] [Full-text]
7. Slow virus disease: deciphering conflicting data on the transmissible spongiform encephalopathies (TSE) also called prion diseases.
   Microsc Res Tech, 68(3): 239-46. [Abstract] [Full-text]
8. Creutzfeldt-Jakob disease acquired via a dural graft: failure of therapy with quinacrine and chlorpromazine.
   Surg Neurol, 64(6): 542-5, discussion 545. [Abstract] [Full-text]
9. Optical coherence tomography in the diagnosis and treatment of neurological disorders.
   J Biomed Opt, 10(5): 51603. [Abstract] [Full-text]
10. Genetic prion disease: the EUROCJD experience.
    Hum Genet, 118(2): 166-74. [Abstract] [Full-text]
11. Dissociation between CSF total tau and tau protein phosphorylated at threonine 231 in Creutzfeldt-Jakob disease.
    Neurobiol Aging, 27(1): 10-5. [Abstract] [Full-text]
12. Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease.
    Lancet Neurol, 4(12): 805-14. [Abstract] [Full-text]
13. Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type.
    Neurology, 65(10): 1544-50. [Abstract] [Full-text]
14. Structures for amyloid fibrils.
    FEBS J, 272(23): 5950-61. [Abstract] [Full-text]
15. Polymorphism at residue 129 modulates the conformational conversion of the D178N variant of human prion protein 90-231.
    Biochemistry, 44(48): 15880-8. [Abstract] [Full-text]
16. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.
    Neurogenetics, 6(4): 229-32. [Abstract] [Full-text]

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