Hostname: page-component-6bf8c574d5-qdpjg Total loading time: 0 Render date: 2025-02-14T23:31:17.352Z Has data issue: false hasContentIssue false
  • English
  • Français

A 67-year-old woman with Parkinsonism

Published online by Cambridge University Press:  24 February 2017

Ging-Yuek R. Hsiung  and
Arthur W. Clark
Ging-Yuek R. Hsiung
Affiliation:
Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada
Arthur W. Clark*
Affiliation:
Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada
*
Department of Pathology and Laboratory Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta, Canada. T2N 4N1
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Neuropathological Conference
Information
Canadian Journal of Neurological Sciences , Volume 28 , Issue 2 , May 2001 , pp. 150 - 154
Copyright
Copyright © The Canadian Journal of Neurological 2001

References

REFERENCES

1. Litvan, I, Agid, Y, Calne, D, et al. Clinical research criteria for progressive supranuclear palsy: report of the NINDS-SPSP international workshop. Neurology 1996;47:1–9.Google Scholar
2. Wenning, GK, Tison, F, Ben-Shlomo, Y, et al. Multiple system atrophy: a review of 203 pathologically proven cases. Mov Disord 1997;12:133–147.Google Scholar
3. Gibb, WR, Luthert, PJ, Janota, I, et al. Cortical Lewy body dementia: clinical features and classification. J Neurol Neurosurg Psychiatry 1989;52:185–192.CrossRefGoogle ScholarPubMed
4. Pillon, B, Dubois, B, Ploska, A, Agid, Y. Severity and specificity of cognitive impairment in Alzheimer’s disease, Huntington’s and Parkinson’s diseases, and progressive supranuclear palsy. Neurology 1991;41:634–643.CrossRefGoogle ScholarPubMed
5. Wright, BA, Rosen, JR, Buysse, DJ, et al. Shy-Drager syndrome presenting as a REM behaviour disorder. J Geriatr Psychiatry Neurol 1990;3:110–113.CrossRefGoogle Scholar
6. Saboiardo, M, Girotti, F, Strada, L, Ciceri, E. MRI in progressive supranuclear palsy and other parkinsonian disorders. J Neural Transm 1994;Suppl 42:93–110.Google Scholar
7. Konagaya, M, Konagaya, Y, Iida, M. Clinical and MRI study of extrapyramidal symptoms in multiple system atrophy. J Neurol Neurosurg Psychiatry 1994;57:1528–1531.Google Scholar
8. Milton, WJ, Atlas, SW, Lavi, E, et al. Magnetic Resonance Imaging of Creutzfeldt-Jacob disease. Ann Neurol 1991;29:438–440.Google Scholar
9. Finkenstaedt, M, Szudra, A, Zerr, I, et al. MR imaging of Creutzfeldt-Jakob disease. Radiology 1996; 199:793–798.CrossRefGoogle ScholarPubMed
10. Demaerel, P, Heiner, L, Robberecht, W, et al. Diffusion-weighted MRI in sporadic Creutzfeldt-Jakob disease. Neurology 1999;52:205–208.Google Scholar
11. Bahn, MM, Parchi, P. Abnormal diffusion-weighted MRI in Creutzfeldt-Jakob disease. Arch Neurol 1999;56:577–583.Google Scholar
12. Duk, LN, Chung, KS, Seong, HY, et al. Diffusion-weighted MRI in probable Creutzfeldt-Jakob disease. Arch Neurol 1999;56:951–957.Google Scholar
13. Magalhaes, ACA, Caramelli, P, Menezes, JR, et al. Wilson’s disease: MRI with clinical correlation. Neuroradiology 1994;36:97–100.CrossRefGoogle ScholarPubMed
14. Zochodne, DW, Young, GB, McLachlan, RS, et al. Creutzfeldt-Jakob disease without periodic sharp wave complexes: a clinical, electroencephalographic, and pathologic study. Neurology 1988; 38:1056–1060.Google Scholar
15. Vingerhoets, FJG, Hegyi, I, Aguzzi, A, et al. An unusual case of Creutzfeldt-Jakob disease. Neurology 1998;51:617–619.Google Scholar
16. Ezrin-Waters, C, Resch, L, Lang, AE. Coexistence of idiopathic Parkinson’s disease and Creutzfeldt-Jakob disease. Can J Neurol Sci 1985;3:272–273.Google Scholar