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Case 31 - Progressive mental decline and fever

from Part II - Uncommon cases of stroke

Published online by Cambridge University Press:  23 November 2009

Michael G. Hennerici
Affiliation:
Universität Mannheim, Germany
Michael Daffertshofer
Affiliation:
Universität Mannheim, Germany
Louis R. Caplan
Affiliation:
Harvard University, Massachusetts
Kristina Szabo
Affiliation:
Universität Mannheim, Germany
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Summary

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Type
Chapter
Information
Case Studies in Stroke
Common and Uncommon Presentations
, pp. 137 - 140
Publisher: Cambridge University Press
Print publication year: 2006

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References

Sourander, P. & Walinder, J.Hereditary multi-infarct dementia: morphological and clinical studies of a new disease. Acta Neuropathol. (Berlin) 1977; 39:247–254.CrossRefGoogle ScholarPubMed
Chabriat, H., Joutel, A., Vahedi, K.et al. [CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging]. Bull. Acad. Natl Med. 2000; 184:1523–1531; discussion 1531–1533.Google Scholar
Joutel, A., Favrole, P., Labauge, P.et al. Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis. Lancet 2001; 358:2049–2051.CrossRefGoogle ScholarPubMed
Joutel, A., Francois, A., Chabriat, H.et al. [CADASIL: genetics and physiopathology]. Bull. Acad. Natl Med. 2000; 184:1535–1542; discussion 1542–1544.Google Scholar
O'Sullivan, M., Jarosz, J. M., Martin, R. J., Deasy, N., Powell, J. F., & Markus, H. S.magnetic resonance imaging hyperintensities of the temporal lobe and external capsule in patients with CADASIL. Neurology 2001; 56:628–634.CrossRefGoogle ScholarPubMed
Verreault, S., Joutel, A., Riant, F.et al. A novel hereditary small vessel disease of the brain. Ann. Neurol. 2006; 59:353–357.CrossRefGoogle Scholar

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