Log in to save to my catalogue

Laboratory Diagnosis of Creutzfeldt–Jakob Disease

Laboratory Diagnosis of Creutzfeldt–Jakob Disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2648064816

Laboratory Diagnosis of Creutzfeldt–Jakob Disease

About this item

Full title

Laboratory Diagnosis of Creutzfeldt–Jakob Disease

Author / Creator

Publisher

United States: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2022-04, Vol.386 (14), p.1345-1350

Language

English

Formats

Publication information

Publisher

United States: Massachusetts Medical Society

More information

Scope and Contents

Contents

The diagnosis of Creutzfeldt–Jakob disease has advanced from detection of characteristic EEG and MRI features to include the detection in CSF of 14-3-3 protein and, with the use of RT-QuIC assays, of abnormally folded prion protein, with close to 100% sensitivity and specificity.

Alternative Titles

Full title

Laboratory Diagnosis of Creutzfeldt–Jakob Disease

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2648064816

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2648064816

Other Identifiers

ISSN

0028-4793

E-ISSN

1533-4406

DOI

10.1056/NEJMra2119323

How to access this item