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Article

Characterization of movement disorders in patients with familial Creutzfeldt-Jakob disease carrying the E200K mutation.

The Israel Medical Association journal : IMAJ - 1 Mar 2012

Cohen Oren S, Prohovnik Isak, Korczyn Amos D, Inzelberg Rivka, Nitsan Zeev, Appel Shmuel, Kahana Ester, Rosenmann Hanna, Chapman Joab

Abstract excerpt

BACKGROUND: While myoclonus and ataxia are considered common in patients with familial Creutzfeld-Jakob disease (fCJD), other movement disorders are less prevalent. OBJECTIVES: To systemically evaluate the frequency of extrapyramidal signs and movement disorders in patients with fCJD. METHODS: A detailed neurological examination, with special emphasis on movement disorders and extrapyramidal signs, was conducted...

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PMID: 22675855

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Characterization of movement disorders in patients with familial Creutzfeldt-Jakob disease carrying the E200K mutation.PMID 22675855Read ↗

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