An unusual case of Creutzfeldt-Jakob disease

Neurology

Volumn 51, Issue 2, 1998, Pages 617-619

  Vingerhoets, F J G ^a   Hegyi, I ^b   Aguzzi, A ^b   Myers, P ^b   Pizzolato, G ^b   Landis, T ^b  

^a LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CREUTZFELDT JAKOB DISEASE; DIFFERENTIAL DIAGNOSIS; DIPLOPIA; DISEASE CLASSIFICATION; HUMAN; MALE; PARKINSONISM; PRIORITY JOURNAL; SLEEP DISORDER;

EID: 0031753427     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.51.2.617     Document Type: Article

References (10)

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2. Budka H, Aguzzi A, Brown P, et al. Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 1995;5:319-322.
3. Kretzschmar HA, Ironside JW, DeArmond SJ, Tateishi J. Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Arch Neurol 1996;53:913-920.
4. Hsich G, Kenney K, Gibbs CJ, Lee KH, Harrington MG. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 1996;335:924-930.
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7. Brown P, Gibbs CJ, Rodgers-Johnson P, et al. Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 1994;35:513-529.
8. Brown P, Cathala F, Castaigne P, Gajdusek DC. Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 1986;20:597-602.
9. Will RG, Matthews WB. A restrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979. I: Clinical features. J Neurol Neurosurg Psychiatry 1984;47:134-140.
10. Brown P, Cathala F. Creutzfeldt-Jakob disease in France: I. Retrospective study of the Paris area during the ten-year period 1968-1977. Ann Neurol 1979;5:189-192.