Diagnostic value of surrogate CSF biomarkers for Creutzfeldt–Jakob disease in the era of RT-QuIC
Author:
Funder
Ministero della Salute
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-019-09537-0.pdf
Reference30 articles.
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3. Parchi P, Strammiello R, Notari S et al (2009) Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification. Acta Neuropathol 118:659–671
4. Parchi P, de Boni L, Saverioni D et al (2012) Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA. Acta Neuropathol 124:517–529
5. Baiardi S, Capellari S, Bartoletti Stella A, Parchi P (2018) Unusual clinical presentations challenging the early clinical diagnosis of Creutzfeldt–Jakob disease. J Alzheimers Dis 64:1051–1065
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