Autoimmune encephalitis mimicking sporadic Creutzfeldt-Jakob disease: A retrospective study
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We present clinical, imaging findings of autoimmune encephalopathies (AE) and sporadic Creutzfeldt-Jakob disease (CJD).

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We compare clinical presentation, signs and outcome of patients with AE and sCJD patients.

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We emphasize the importance of early diagnosis and treatment on outcome.

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Correct discrimination between myoclonus-like movements and myoclonus is paramount for early identification.

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