Early and long-term cognitive features in sporadic Creutzfeldt-Jakob disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s10072-021-05201-6.pdf
Reference6 articles.
1. Baiardi S, Capellari S, Bartoletti SA, Parchi P (2018) Unusual clinical presentations challenging the early clinical diagnosis of Creutzfeldt-Jakob disease. JAD 64:1051–1065. https://doi.org/10.3233/jad-180123
2. Giovagnoli AR, Tallarita G, Parente A, Del Sole A, Di Fede G (2018) A new neurobehavioral phenotype of familial Creutzfeldt–Jakob disease: impaired theory of mind. Neurol Sci 40:1073–1075. https://doi.org/10.1007/s10072-018-3646-1
3. Caverzasi E, Mandelli ML, DeArmond SJ, Hess CP, Vitali P, Papinutto N, Oehler A, Miller BL, Lobach IV, Bastianello S, Geschwind MD, Henry RG (2014) White matter involvement in sporadic Creutzfeldt-Jakob disease. Brain 137:3339–3354. https://doi.org/10.1093/brain/awu298
4. Reuber M, Al-Din ASN, Baborie A, Chakrabarty A (2001) New variant Creutzfeldt-Jakob disease presenting with loss of taste and smell. J Neurol Neurosurg Psychiatry 71:412–413. https://doi.org/10.1136/jnnp.71.3.412
5. Kobylecki C, Thompson JC, Jones M, Mills SJ, Shaunak S, Ironside JW, Snowden JS, Richardson AM (2013) Sporadic Creutzfeldt-Jakob disease presenting as progressive nonfluent aphasia with speech apraxia. Alzheimer Dis Assoc Disord 27:384–386. https://doi.org/10.1097/WAD.0b013e318260ab27
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1. The cognitive phenotypes of Creutzfeldt-Jakob disease: comparison with secondary metabolic encephalopathy;Neurological Sciences;2022-01-28
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