Creutzfeldt-Jakob disease presenting as progressive supranuclear palsy

European Journal of Neurology

Volumn 11, Issue 5, 2004, Pages 343-346

  Josephs, K A ^a   Tsuboi, Y ^a   Dickson, D W ^a  

^a MAYO CLINIC   (United States)

Author keywords

Creutzfeldt Jakob disease; Progressive supranuclear palsy; Vertical supranuclear ophthalmoplegia

Indexed keywords

LEVODOPA; TAU PROTEIN;

AGED; ARTICLE; CASE REPORT; CEREBROSPINAL FLUID; COGNITIVE DEFECT; CORTICOBASAL DEGENERATION; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIAGNOSTIC ERROR; ELECTROENCEPHALOGRAM; FALLING; FEMALE; GAIT DISORDER; HUMAN; MENTAL HEALTH; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSONISM; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; VISUAL DISORDER; WHEELCHAIR; BRAIN; COMPARATIVE STUDY; IMMUNOHISTOCHEMISTRY; MALE; METABOLISM; METHODOLOGY; NERVE CELL; NEUROLOGIC EXAMINATION; PATHOLOGY; STAINING;

AGED; BRAIN; CREUTZFELDT-JAKOB SYNDROME; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; NEUROLOGIC EXAMINATION; NEURONS; STAINING AND LABELING; SUPRANUCLEAR PALSY, PROGRESSIVE; TAU PROTEINS;

EID: 2942754064     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2004.00780.x     Document Type: Article

References (18)

1. Alafuzoff I, Hartikainen P, Hanninen T et al. (1999). Rapidly progressive multifocal leukoencephalopathy with substantial cell-mediated inflammatory response and with cognitive decline of non-Alzheimer type in a 75-year-old female patient. Clin Neuropathol 18:113-123.
2. Averbuch-Heller L, Paulson GW, Daroff RB, Leigh RJ (1999). Whipple's disease mimicking progressive supranuclear palsy: the diagnostic value of eye movement recording. J Neurol Neurosurg Psychiatry 66:532-535.
3. Bertoni JM, Brown P, Goldfarb LG, Rubenstein R, Gajdusek DC (1992). Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy. JAMA 268:2413-2415.
4. Budka H, Aguzzi A, Brown P et al. (1995). Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). Brain Pathol 5:459.
5. Hauw JJ, Daniel SE, Dickson D et al. (1994). Preliminary NINDS neuropathologic criteria for Steele-Richardson- Olszewski syndrome (progressive supranuclear palsy). Neurology 4:2015-2019.
6. Josephs KA, Dickson DW (2003). Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy Brain Bank. Mov Disord 18:1018-1026.
7. Josephs KA, Ishizawa T, Tsuboi Y, Cookson N, Dickson DW (2002). A clinicopathological study of vascular progressive supranuclear palsy: a multi-infarct disorder presenting as progressive supranuclear palsy. Arch Neurol 59:1597-1601.
8. Lee RG, Blair RD (1973). Evolution of EEG and visual evoked response changes in Jakob-Creutzfeldt disease. Electroencephalogr Clin Neurophysiol 35:133-142.
9. Litvan I, Agid Y, Calne D et al. (1996). Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP International Workshop. Neurology 47:1-9.
10. Lueck CJ, McIlwaine GG, Zeidler M (2000). Creutzfeldt- Jakob disease and the eye. II. Ophthalmic and neuroophthalmic features. Eye 14:291-301.
11. Murialdo A, Marchese R, Abbruzzese G, Massimo T, Michelozzi G, Schiavoni S (2000). Neurosyphilis presenting as progressive supranuclear palsy. Mov Disord 15:730-731.
12. Pramstaller PP, Lees AJ, Luxon LM (1996). Possible overlap between postencephalitic parkinsonism and progressive supranuclear palsy. J Neurol Neurosurg Psychiatry 60:589-590.
13. Revesz T, Sangha H, Daniel SE (1996). The nucleus raphe interpositus in the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy). Brain 119:1137-1143.
14. Russell RW (1980). Supranuclear palsy of eyelid closure. Brain 103:71-82.
15. Schroter A, Zerr I, Henkel K, Tschampa HJ, Finkenstaedt M, Poser S (2000). Magnetic resonance imaging in the clinical diagnosis of Creutzfeldt-Jakob disease. Arch Neurol 57:1751-1757.
16. Shimamura M, Uyama E, Hirano T et al. (2003). A unique case of sporadic Creutzfieldt-Jacob disease presenting as progressive supranuclear palsy. Intern Med 42:195-198.
17. Steele JC, Richardson JC, Olszewski J (1964). Progressive supranuclear palsy. Arch Neurol 10:333-359.
18. Zerr I, Pocchiari M, Collins S et al. (2000). Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology 55:811-815.