Rapidly progressive dementia with focal symptoms: when to suspect Creutzfeldt–Jakob disease?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s13760-023-02332-9.pdf
Reference8 articles.
1. Hermann P, Zerr I (2022) Rapidly progressive dementias—Aetiologies, diagnosis and management. Nat Rev Neurol 18(6):363–376
2. Krasnianski A, Kaune J, Jung K, Kretzschmar HA, Zerr I (2014) First symptom and initial diagnosis in sporadic CJD patients in Germany. J Neurol 261(9):1811–1817
3. Baiardi S, Capellari S, Stella AB, Parchi P (2018) Unusual clinical presentations challenging the early clinical diagnosis of Creutzfeldt-Jakob disease. J Alzheimer’s Dis 64(4):1051–1065
4. Wu H, Lu C, Huang C, Lyu R (2010) Asymmetric involvement in sporadic Creutzfeldt-Jakob disease: clinical, brain imaging, and electroencephalographic studies. Eur Neurol 64:74–79
5. National CJD Research & Surveilance Unit. CJD diagnostic criteria: guidance for clinicians, 2017, 1–5, Accessed 15th Feb 2023
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