Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
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Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathyMolecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision MedicineThe Priority position paper: Protecting Europe's food chain from prionsRapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Neuroradiology of human prion diseases, diagnosis and differential diagnosis.Altered Ca2+ homeostasis induces Calpain-Cathepsin axis activation in sporadic Creutzfeldt-Jakob diseaseSubtype and regional-specific neuroinflammation in sporadic creutzfeldt-jakob disease.A test for Creutzfeldt-Jakob disease using nasal brushings.No reactivation of JCV and CMV infections in the temporal cortex and cerebellum of sporadic Creutzfeldt-Jakob disease patients.Mathematical models for the diffusion magnetic resonance signal abnormality in patients with prion diseases.Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid.Structural determinants of phenotypic diversity and replication rate of human prions.The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease PatientsInactivation of Prions and Amyloid Seeds with Hypochlorous Acid.Cystatin F is a biomarker of prion pathogenesis in mice.Detection of Atypical H-Type Bovine Spongiform Encephalopathy and Discrimination of Bovine Prion Strains by Real-Time Quaking-Induced Conversion.Dura mater is a potential source of Aβ seeds.Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory FindingsIatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein geneDeciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein.Diagnostic Accuracy of a Combined Analysis of Cerebrospinal Fluid t-PrP, t-tau, p-tau, and Aβ42 in the Differential Diagnosis of Creutzfeldt-Jakob Disease from Alzheimer's Disease with Emphasis on Atypical Disease Variants.Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels.UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approachesHuman prion diseases: molecular, cellular and population biology.Prion disease: a tale of folds and strains.Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases.Validation of α-Synuclein as a CSF Biomarker for Sporadic Creutzfeldt-Jakob Disease.Inconsistency in the analysis of morphological deformities in chironomidae (Insecta: Diptera) larvae.Diagnostic and prognostic value of human prion detection in cerebrospinal fluid.Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK.High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions.An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature.Regional and subtype-dependent miRNA signatures in sporadic Creutzfeldt-Jakob disease are accompanied by alterations in miRNA silencing machinery and biogenesis.Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry.Sisyphus in Neverland.A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles.Plasma and cerebrospinal fluid tau and neurofilament concentrations in rapidly progressive neurological syndromes: a neuropathology-based cohort.The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias.
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Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 30 June 2012
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Consensus classification of hu ...... ance centres in Europe and USA
@en
Consensus classification of hu ...... nce centres in Europe and USA.
@nl
type
label
Consensus classification of hu ...... ance centres in Europe and USA
@en
Consensus classification of hu ...... nce centres in Europe and USA.
@nl
prefLabel
Consensus classification of hu ...... ance centres in Europe and USA
@en
Consensus classification of hu ...... nce centres in Europe and USA.
@nl
P2093
P2860
P50
P1476
Consensus classification of hu ...... ance centres in Europe and USA
@en
P2093
Annemieke Rozemuller
Casper Jansen
Daniela Saverioni
Danielle Seilhean
Ellen Gelpi
Giorgio Giaccone
Hans A Kretzschmar
Isidro Ferrer
Laura de Boni
Mark L Cohen
P2860
P2888
P304
P356
10.1007/S00401-012-1002-8
P577
2012-06-30T00:00:00Z