Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3042069 | Clinical Neurology and Neurosurgery | 2007 | 4 Pages |
Abstract
In a patient with a rapidly progressive neurological condition with ataxia and cognitive complaints, Creutzfeldt–Jakob disease (CJD) is often high in the differential, particularly when there is an elevated CSF 14-3-3 protein level. We present a case of anti-glutamic acid decarboxylase antibody (anti-GAD65) positive cerebellar ataxia associated with cognitive complaints and elevated CSF 14-3-3 protein.
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Authors
Chiung-Chih Chang, Scott D. Eggers, Julene K. Johnson, Aissa Haman, Bruce L. Miller, Michael D. Geschwind,