A test for Creutzfeldt-Jakob disease using nasal brushings. - Test2 - elhamkhani - TriplyDB

A test for Creutzfeldt-Jakob disease using nasal brushings.

A test for Creutzfeldt-Jakob disease using nasal brushings.

http://www.wikidata.org/entity/Q34293962

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Biomarkers for sporadic Creutzfeldt-Jakob disease Principles of infection prevention and reprocessing in ENT endoscopy Changes in retinal function and morphology are early clinical signs of disease in cattle with bovine spongiform encephalopathy Human prion diseases: surgical lessons learned from iatrogenic prion transmission Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia Advanced tests for early and accurate diagnosis of Creutzfeldt-Jakob disease.Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains Holocranohistochemistry enables the visualization of α-synuclein expression in the murine olfactory system and discovery of its systemic anti-microbial effects A Case Report of Probable Sporadic Creutzfeldt-Jakob Disease: How to Approach Early Diagnosis?Quantitative assessment of prion infectivity in tissues and body fluids by real-time quaking-induced conversion.Rapid and sensitive RT-QuIC detection of human Creutzfeldt-Jakob disease using cerebrospinal fluid.Detection and discrimination of classical and atypical L-type bovine spongiform encephalopathy by real-time quaking-induced conversion Lesion of the olfactory epithelium accelerates prion neuroinvasion and disease onset when prion replication is restricted to neurons.Identification of novel putative-binding proteins for cellular prion protein and a specific interaction with the STIP1 homology and U-Box-containing protein 1.Creutzfeldt-Jakob Disease in a Tertiary Care Hospital in Thailand: A Case Series and Review of the Literature Longitudinal Detection of Prion Shedding in Saliva and Urine by Chronic Wasting Disease-Infected Deer by Real-Time Quaking-Induced Conversion.2005 Donor Eligibility Requirements: Unintended Consequences for Stem Cell Development.Inactivation of Prions and Amyloid Seeds with Hypochlorous Acid.Anti-Prion Screening for Acridine, Dextran, and Tannic Acid using Real Time-Quaking Induced Conversion: A Comparison with PrPSc-Infected Cell Screening Use of bovine recombinant prion protein and real-time quaking-induced conversion to detect cattle transmissible mink encephalopathy prions and discriminate classical and atypical L- and H-Type bovine spongiform encephalopathy.Detection and partial discrimination of atypical and classical bovine spongiform encephalopathies in cattle and primates using real-time quaking-induced conversion assay.Real-Time Quaking-Induced Conversion Analysis for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease in Korea Early diagnosis of Alzheimer's disease from elevated olfactory mucosal miR-206 level.Detection of Atypical H-Type Bovine Spongiform Encephalopathy and Discrimination of Bovine Prion Strains by Real-Time Quaking-Induced Conversion.Seeded Amplification of Chronic Wasting Disease Prions in Nasal Brushings and Recto-anal Mucosa-Associated Lymphoid Tissues from Elk by Real-Time Quaking-Induced Conversion.Antemortem Detection of Chronic Wasting Disease Prions in Nasal Brush Collections and Rectal Biopsy Specimens from White-Tailed Deer by Real-Time Quaking-Induced Conversion Factors That Improve RT-QuIC Detection of Prion Seeding Activity.Prions: Beyond a Single Protein.A rare case of rapidly progressive dementia with elevated RT-QuIC and negative 14-3-3 and tau proteins.Extended and direct evaluation of RT-QuIC assays for Creutzfeldt-Jakob disease diagnosis Integrated Organotypic Slice Cultures and RT-QuIC (OSCAR) Assay: Implications for Translational Discovery in Protein Misfolding Diseases.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.Proteomics applications in prion biology and structure.A practical approach to avoiding iatrogenic Creutzfeldt-Jakob disease (CJD) from invasive instruments.A novel diagnostic approach to patients with myoclonus.Pathways of Prion Spread during Early Chronic Wasting Disease in Deer.Sporadic and Infectious Human Prion Diseases.Insights from Therapeutic Studies for PrP Prion Disease.Corticobasal syndrome due to sporadic Creutzfeldt-Jakob disease: a review and neuropsychological case report.Detection of prions in the plasma of presymptomatic and symptomatic patients with variant Creutzfeldt-Jakob disease.

P2860

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P2860

A test for Creutzfeldt-Jakob disease using nasal brushings.

http://www.wikidata.org/entity/Q34293962

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

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name

A test for Creutzfeldt-Jakob disease using nasal brushings.

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A test for Creutzfeldt-Jakob disease using nasal brushings.

@en

A test for Creutzfeldt-Jakob disease using nasal brushings.

@nl

type

label

A test for Creutzfeldt-Jakob disease using nasal brushings.

@ast

A test for Creutzfeldt-Jakob disease using nasal brushings.

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A test for Creutzfeldt-Jakob disease using nasal brushings.

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prefLabel

A test for Creutzfeldt-Jakob disease using nasal brushings.

@ast

A test for Creutzfeldt-Jakob disease using nasal brushings.

@en

A test for Creutzfeldt-Jakob disease using nasal brushings.

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The New England Journal of Medicine

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A test for Creutzfeldt-Jakob disease using nasal brushings.

@en

P2093

Andrew G Hughson

http://www.w3.org/2001/XMLSchema#string

Bradley R Groveman

http://www.w3.org/2001/XMLSchema#string

Christina D Orrú

http://www.w3.org/2001/XMLSchema#string

Giovanni Tonoli

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Matilde Bongianni

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Sergio Ferrari

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P2860

Aerosols transmit prions to immunocompetent and immunodeficient mice

Generating a prion with bacterially expressed recombinant prion protein.

Recombinant prion protein induces a new transmissible prion disease in wild-type animals.

Formation of native prions from minimal components in vitro

Prion shedding from olfactory neurons into nasal secretions

Two-sided confidence intervals for the single proportion: comparison of seven methods

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

Getting a grip on prions: oligomers, amyloids, and pathological membrane interactions.

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

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519-529

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scholarly article

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10.1056/NEJMOA1315200

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P433

6

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371

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Gianluigi Zanusso

Maurizio Pocchiari

Salvatore Monaco

Michele Fiorini

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2014-08-01T00:00:00Z

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25099576

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4186748

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