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Andrew Geoffrey Bourne Thompson et al.
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Plasma and cerebrospinal fluid tau and neurofilament concentrations in rapidly progressive neurological syndromes: a neuropathology-based cohort
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Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type)
Simone Baiardi et al.
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Alessia Franceschini et al.
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Francesca Lattanzio et al.
ACTA NEUROPATHOLOGICA (2017)
Diagnostic and prognostic value of human prion detection in cerebrospinal fluid
Aaron Foutz et al.
ANNALS OF NEUROLOGY (2017)
Neurofilaments in blood and CSF for diagnosis and prediction of onset in Creutzfeldt-Jakob disease
Petra Steinacker et al.
SCIENTIFIC REPORTS (2016)
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
Piero Parchi et al.
ACTA NEUROPATHOLOGICA (2012)
Sporadic human prion diseases: molecular insights and diagnosis
Gianfranco Puoti et al.
LANCET NEUROLOGY (2012)
A comparison of tau and 14-3-3 protein in the diagnosis of Creutzfeldt-Jakob disease
Clive Hamlin et al.
NEUROLOGY (2012)
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
Piero Parchi et al.
BRAIN (2010)
The role of cerebrospinal fluid 14-3-3 and other proteins in the diagnosis of sporadic Creutzfeldt-Jakob disease in the UK: a 10-year review
G. Chohan et al.
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Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis
Pascual Sanchez-Juan et al.
JOURNAL OF NEUROLOGY (2007)
Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies
M Pocchiari et al.
BRAIN (2004)