Creutzfeldt-Jakob Disease Diagnosable by EEG and Cerebrospinal Fluid Analysis without Brain Biopsy: A Case Report

Gambetti P Parchi P . Insomnia in prion disease: Sporadic and familial. Editorials. N Engl J Med 1999: 340; 1675–1677.

Mastrianni JA Nizon R Telling GC . Prion protein conformation in a patient with sporadic fatal insomnia. N Engl J Med 1999: 340; 1630–1638.

Hsieh G Kenney K Gibbs CJ . The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 1996; 335: 924–930.

Creuzfeldt HG . Über eine eigenartige herdförmige Erkrankung des Zentralnervensystems. Neural Psychiatr 1920; 57: 1–9.

Prusiner SVB. Prion diseases and the BSE crisis. Science 1997; 278: 245–251.

Grady D . Ironing out the wrinkles in the prion strain problem. Science 1996; 274: 2079–2082.

Kretzschmar HA Ironside JW DeArmond SJ . Diagnostic criteria for Creutzfeldt-Jakob disease. Arch Neurol 1996; 9: 913–920.

Brown P . The risk of bovine spongiform encephalopathy (‘mad cow disease’) to human health. JAMA 278; 1997: 1008–1011.

Will RG Ironside JW Zeidler M . A new variant of Creuzfeldt-Jakob disease in the U.K. Lancet. 1996; 347: 921–925.

Will R Zeidler M . Diagnosing Creuzfeldt-Jakob disease. BMJ 1996; 313: 833–834.

Steinhoff BJ Racker S Herrendorf G . Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease. Arch Neurol 1996; 53: 162–166.

Brown P . Environmental causes of human spongiform encephalopathy. In: Baker H Ridgely R (eds). Methods in Molecular Medicine: Prion Diseases. Totowa, NJ: Humana Press; 1996; 139–154.

Bernad PG . Creutzfeldt-Jakob disease, human growth hormone and its replacement with synthetic growth hormone. Proceedings of the Third International Conference on Pharmacoepidemiology. 1987; University of Minnesota, Minneapolis.

Bernad PG . Guidelines: Relevance of infectious diseases for the electroencephalogram and other neurophysiology laboratories. Clin Electroencephalogr 1989; 20(3): VIII–X.