Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium
Author:
Publisher
Springer Science and Business Media LLC
Subject
Epidemiology
Link
http://link.springer.com/content/pdf/10.1007/s10654-006-9012-2.pdf
Reference24 articles.
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3. Hill AF, Desbruslais M, Joiner S, Sidle KCL, Gowland I, Collinge J, et al. (1997) The same prion strain causes vCJD and BSE. Nature 389:448–450
4. Zerr I, Pocchiari M, Collins S, Brandel JP, Cuesta JD, Knight RSG, et al. (2000) Analysis of EEG and CSF 14-3-3 protein as aids to the diagnosis of Creutzfeldt-Jakob disease. Neurology 55:811–815
5. Otto M, Wiltfang J, Tumani H, Zerr I, Lantsch M, Kornhuber J, et al. (1997) Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. Neurosci Lett 225:210–212
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