(Q35815746)

10 August 2017

The Features of Genetic Prion Diseases Based on Chinese Surveillance Program (English)

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10 August 2017

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1

Qi Shi

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10 August 2017

16

Xiao-Ping Dong

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10 August 2017

Wei Zhou

2

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10 August 2017

Cao Chen

3

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10 August 2017

Bao-Yun Zhang

4

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10 August 2017

Kang Xiao

5

1 reference

10 August 2017

Xiu-Chun Zhang

6

1 reference

10 August 2017

Xiao-Jing Shen

7

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10 August 2017

Qing Li

8

1 reference

10 August 2017

Li-Quan Deng

9

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10 August 2017

Jian-Hua Dong

10

1 reference

10 August 2017

Wen-Qing Lin

11

1 reference

10 August 2017

Pu Huang

12

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10 August 2017

Wei-Jia Jiang

13

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10 August 2017

Jie Lv

14

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10 August 2017

Jun Han

15

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10 August 2017

language of work or name

English

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publication date

21 October 2015

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10 August 2017

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10 August 2017

10

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10 August 2017

10

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10 August 2017

e0139552

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Creative Commons Attribution 4.0 International

10 August 2017

start time

21 October 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Analysis of the advantage features of Beijing surveillance network for Creutzfeldt-Jakob disease

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Genetic studies in human prion diseases.

27 July 2018

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Brain microglia were activated in sporadic CJD but almost unchanged in fatal familial insomnia and G114V genetic CJD.

27 July 2018

1 reference

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Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.

27 July 2018

1 reference

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An overview of human prion diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.

27 July 2018

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The epidemiological, clinical, and laboratory features of sporadic Creutzfeldt-Jakob disease patients in China: surveillance data from 2006 to 2010

27 July 2018

1 reference

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A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature

27 July 2018

1 reference

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Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

27 July 2018

1 reference

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Surveillance for Creutzfeldt-Jakob disease in China from 2006 to 2007.

27 July 2018

1 reference

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Human prion disease with a G114V mutation and epidemiological studies in a Chinese family: a case series

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Evidence for a pathogenic role of different mutations at codon 188 of PRNP

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

De novo seven extra repeat expanded mutation in the PRNP gene in an Italian patient with early onset dementia.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Creutzfeldt-Jakob disease mortality in Japan, 1979-2004: analysis of national death certificate data

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Clinical diagnosis and differential diagnosis of CJD and vCJD. With special emphasis on laboratory tests

27 July 2018

1 reference

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Genetic epidemiology of Creutzfeldt-Jakob disease in Europe

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Molecular studies of prion diseases

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Surveillance for Creutzfeldt-Jakob disease in Australia: update to December 2012.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Comparison of the pathologic and pathogenic features in six different regions of postmortem brains of three patients with fatal familial insomnia

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Variability in diagnosing Creutzfeldt-Jakob disease using standard and proposed diagnostic criteria

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Clinical and familial characteristics of ten chinese patients with fatal family insomnia

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

The diversities of PrP(Sc) distributions and pathologic changes in various brain regions from a Chinese patient with G114V genetic CJD.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Prospective 10-year surveillance of human prion diseases in Japan.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Clinical, histopathological and genetic studies in a family with fatal familial insomnia

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

24 September 2018

Prion disease genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Genetic prion disease: the EUROCJD experience.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Comparison study on clinical and neuropathological characteristics of hamsters inoculated with scrapie strain 263K in different challenging pathways

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

High incidence of Creutzfeldt-Jakob disease in rural Calabria, Italy

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4619501

High frequency of mutations in four different disease genes in early-onset dementia

24 September 2018

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy

1 reference

PubMed

12 December 2020

Creutzfeldt-Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP

1 reference

PubMed

12 December 2020

10.1371/JOURNAL.PONE.0139552

Identifiers

DOI

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10 August 2017

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10 August 2017

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