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 9 (September)

1. Cyclooxygenases, lipoxygenases, and epoxygenases in CNS: their role and involvement in neurological disorders.
   Brain Res Brain Res Rev, 52(2): 201-43. [Abstract] [Full-text]
2. Depressive disorder with psychotic symptoms as psychiatric presentation of sporadic Creutzfeldt-Jakob disease: a case report.
   Gen Hosp Psychiatry, 28(5): 452-4. [Abstract] [Full-text]
3. Unilateral positive-negative myoclonus in Creutzfeldt-Jakob disease.
   Mov Disord. [Abstract] [Full-text]
4. Creutzfeldt-Jakob disease and blood transfusion: results of the UK Transfusion Medicine Epidemiological Review study.
   Vox Sang, 91(3): 221-30. [Abstract] [Full-text]
5. Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob disease.
   J Gen Virol, 87: 3119-24. [Abstract] [Full-text]
6. Transplantation of ocular tissue from a donor with sporadic Creutzfeldt-Jakob disease.
   Clin Experiment Ophthalmol, 34(7): 645-9. [Abstract] [Full-text]
7. Quantitative evaluation of prion inactivation comparing steam sterilization and chemical sterilants: proposed method for test standardization.
   J Hosp Infect, 64(2): 143-8. [Abstract] [Full-text]
8. Dividing roles of prion protein in staurosporine-mediated apoptosis.
   Biochem Biophys Res Commun, 349(2): 759-68. [Abstract] [Full-text]
9. Are amyloid diseases caused by protein aggregates that mimic bacterial pore-forming toxins?
   Q Rev Biophys. [Abstract] [Full-text]
10. Balancing evidence and public opinion in health technology assessments: the case of leukoreduction.
    Int J Technol Assess Health Care, 22(4): 403-7. [Abstract] [Full-text]
11. Myiasis as a risk factor for prion diseases in humans.
    J Eur Acad Dermatol Venereol, 20(9): 1037-45. [Abstract] [Full-text]
12. Directed evolution of an anti-prion protein scFv fragment to an affinity of 1 pM and its structural interpretation.
    J Mol Biol, 363(1): 75-97. [Abstract] [Full-text]
13. MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology.
    Acta Neuropathol (Berl), 112(4): 503-11. [Abstract] [Full-text]

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