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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
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Abstract

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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