(Q31095751)

28 June 2017

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title

Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease (English)

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Creutzfeldt-Jakob disease

28 June 2017

main subject

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Maurizio Pocchiari

3

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Byron Caughey

series ordinal

4

object named as

Byron Caughey

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28 June 2017

Gianluigi Zanusso

1

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28 June 2017

Salvatore Monaco

series ordinal

2

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28 June 2017

language of work or name

English

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publication date

13 May 2016

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28 June 2017

published in

Nature Reviews Neurology

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28 June 2017

volume

12

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28 June 2017

issue

6

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28 June 2017

page(s)

325-333

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Protein aggregation diseases: pathogenicity and therapeutic perspectives

28 June 2017

cites work

1 reference

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Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease

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Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.

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Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

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Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias

21 January 2018

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The 14-3-3 protein detectable in the cerebrospinal fluid of patients with prion-unrelated neurological diseases is expressed constitutively in neurons and glial cells in culture

21 January 2018

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Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle

21 January 2018

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21 January 2018

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21 January 2018

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A highly specific blood test for vCJD

21 January 2018

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Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay

21 January 2018

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Stability and Reproducibility Underscore Utility of RT-QuIC for Diagnosis of Creutzfeldt-Jakob Disease

21 January 2018

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21 January 2018

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A test for Creutzfeldt-Jakob disease using nasal brushings

21 January 2018

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21 January 2018

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21 January 2018

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Rapid end-point quantitation of prion seeding activity with sensitivity comparable to bioassays

21 January 2018

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Olfactory bulb involvement in neurodegenerative diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Prions and their partners in crime

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Physiology of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Allosteric function and dysfunction of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Cellular prion protein mediates impairment of synaptic plasticity by amyloid-beta oligomers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Prion protein and susceptibility to kainate-induced seizures: genetic pitfalls in the use of PrP knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Iatrogenic Creutzfeldt-Jakob disease, final assessment

21 January 2018

1 reference

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Protein misfolding cyclic amplification of infectious prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Periodic electroencephalogram complexes in a patient with variant Creutzfeldt-Jakob disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Strategies to reduce transfusion acquired vCJD

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Detection of misfolded Aβ oligomers for sensitive biochemical diagnosis of Alzheimer's disease

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRNEUROL.2016.65

Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies.

31 March 2020

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12 December 2020

Validation of diagnostic criteria for variant Creutzfeldt-Jakob disease

1 reference

12 December 2020

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

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12 December 2020

A Test for Creutzfeldt–Jakob Disease Using Nasal Brushings

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRNEUROL.2016.65

1 reference

Dimensions Publication ID

28 June 2017

1013789764

0 references

1 reference