Clinical course in young patients with sporadic Creutzfeldt-Jakob disease. - Wikidata - wikimedia - TriplyDB

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q30995751

about

Early onset prion disease from octarepeat expansion correlates with copper binding properties Relationship between clinical signs and postmortem test status in cattle experimentally infected with the bovine spongiform encephalopathy agent Therapeutic approaches for prion disorders.Rapidly progressive young-onset dementia.Allosteric function and dysfunction of the prion protein.Clinical and laboratory features of 14 young Chinese probable sCJD patients.Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated with native human growth hormone.Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene.

P2860

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P2860

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

http://www.wikidata.org/entity/Q30995751

description

2005 nî lūn-bûn

@nan

2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

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Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

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type

label

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

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Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

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prefLabel

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

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Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

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P1433

Annals of Neurology

P1476

Clinical course in young patients with sporadic Creutzfeldt-Jakob disease.

@en

P2093

Anna Krasnianski

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

Bettina Meissner

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Constanze Boesenberg

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Daniela Varges

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Hans A Kretzschmar

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Inga Zerr

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Kai Kallenberg

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Katharina Stoeck

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Mario Bartl

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Otto Windl

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P2860

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease.

The paraffin-embedded tissue blot detects PrP(Sc) early in the incubation time in prion diseases.

The epidemiology of Creutzfeldt-Jakob disease: conclusion of a 15-year investigation in France and review of the world literature.

Accuracy and reliability of periodic sharp wave complexes in Creutzfeldt-Jakob disease.

A simple and effective method for inactivating virus infectivity in formalin-fixed tissue samples from patients with Creutzfeldt-Jakob disease.

Molecular genetics of prion diseases in France. French Research Group on Epidemiology of Human Spongiform Encephalopathies.

P304

533-543

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scholarly article

P356

10.1002/ANA.20568

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4

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58

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P577

2005-10-01T00:00:00Z

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P698

16037975

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