(Q38019773)

27 August 2017

title

Sporadic human prion diseases: molecular insights and diagnosis (English)

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27 August 2017

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6

Pierluigi Gambetti

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27 August 2017

Gianfranco Puoti

1

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27 August 2017

Alberto Bizzi

2

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27 August 2017

Gianluigi Forloni

3

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27 August 2017

Jiri G Safar

4

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27 August 2017

Fabrizio Tagliavini

5

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27 August 2017

publication date

1 July 2012

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27 August 2017

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27 August 2017

volume

11

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27 August 2017

issue

7

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27 August 2017

page(s)

618-628

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Experimental transmission of a Kuru-like syndrome to chimpanzees

27 August 2017

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7 January 2021

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7 January 2021

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7 January 2021

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

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7 January 2021

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7 January 2021

Fatal familial insomnia and the widening spectrum of prion diseases

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7 January 2021

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7 January 2021

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7 January 2021

Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease.

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7 January 2021

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7 January 2021

Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification

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7 January 2021

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7 January 2021

Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

SYMPTOMATIC OCCULT HYDROCEPHALUS WITH "NORMAL" CEREBROSPINAL-FLUID PRESSURE.A TREATABLE SYNDROME.

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7 January 2021

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7 January 2021

Clinical changes and EEG patterns preceding the onset of periodic sharp wave complexes in Creutzfeldt-Jakob disease.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Influence of timing on CSF tests value for Creutzfeldt-Jakob disease diagnosis

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7 January 2021

14-3-3 CSF levels in sporadic Creutzfeldt-Jakob disease differ across molecular subtypes

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7 January 2021

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

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7 January 2021

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.

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7 January 2021

Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease.

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7 January 2021

Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease

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7 January 2021

Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease

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7 January 2021

Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement study

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7 January 2021

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

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7 January 2021

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7 January 2021

Serial Diffusion-Weighted MRI of Creutzfeldt-Jakob Disease

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7 January 2021

Diffusion-weighted imaging and magnetic resonance spectroscopy of sporadic Creutzfeldt-Jakob disease: correlation with clinical course.

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7 January 2021

Monoclonal antibodies inhibit prion replication and delay the development of prion disease

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7 January 2021

High titers of mucosal and systemic anti-PrP antibodies abrogate oral prion infection in mucosal-vaccinated mice.

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7 January 2021

Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies.

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7 January 2021

10.1016/S1474-4422(12)70063-7

Identifiers

DOI

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release_tlvevtna5ffedpfwjesn4d3ql4

27 August 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/tlvevtna5ffedpfwjesn4d3ql4

24 November 2022

mapped directly with Wikidata item

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