Epidemiological characteristics of human prion diseases (Q26744136)

23 March 2019

25 April 2019

19 September 2019

on focus list of Wikimedia project

16 December 2020

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copyrighted

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cites work

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7 April 2017

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Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients

7 April 2017

1 reference

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Mutations of the prion protein gene phenotypic spectrum

7 April 2017

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The Features of Genetic Prion Diseases Based on Chinese Surveillance Program

7 April 2017

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Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.

28 September 2017

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

28 September 2017

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Variant CJD. 18 years of research and surveillance

28 September 2017

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Review: Laboratory diagnosis and surveillance of Creutzfeldt-Jakob disease

28 September 2017

1 reference

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Genetic studies in human prion diseases.

28 September 2017

1 reference

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Analyses of the survival time and the influencing factors of chinese patients with prion diseases based on the surveillance data from 2008-2011.

28 September 2017

1 reference

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

28 September 2017

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Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countries

28 September 2017

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Iatrogenic Creutzfeldt-Jakob disease, final assessment

28 September 2017

1 reference

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Genotype patterns and characteristics of PRNP in the Korean population

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects

28 September 2017

1 reference

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

28 September 2017

1 reference

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Diagnostic accuracy of cerebrospinal fluid protein markers for sporadic Creutzfeldt-Jakob disease in Canada: a 6-year prospective study

28 September 2017

1 reference

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Duration of prion disease is longer in Japan than in other countries

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Genetics of prion disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Probable variant Creutzfeldt–Jakob disease in Asia: a case report from Taiwan and review of two prior cases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Familial Creutzfeldt-Jakob disease with V180I mutation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

The genetics of prion diseases

28 September 2017

1 reference

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Human prion diseases in the United States.

28 September 2017

1 reference

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PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

28 September 2017

1 reference

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Prions and prion diseases: fundamentals and mechanistic details.

28 September 2017

1 reference

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Variant Creutzfeldt-Jakob disease: prion protein genotype analysis of positive appendix tissue samples from a retrospective prevalence study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Risk of variant Creutzfeldt-Jakob disease in France.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Acquired prion disease: iatrogenic CJD, variant CJD, kuru

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Sporadic and familial CJD: classification and characterisation.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Genetic epidemiology of Creutzfeldt-Jakob disease in Europe

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

A new variant of Creutzfeldt-Jakob disease in the UK.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Evidence for case-to-case transmission of Creutzfeldt-Jakob disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

A new human genotype prone to variant Creutzfeldt-Jakob disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Molecular analysis of prion protein gene (PRNP) in Korean patients with Creutzfeldt-Jakob disease

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Letter: Possible person-to-person transmission of Creutzfeldt-Jakob disease

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.

31 May 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

[Epidemiological surveillance of Creutzfeldt-Jakob in France].

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Creutzfeldt-Jakob disease among American Indians and Alaska Natives in the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Genetic prion disease: the EUROCJD experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Polymorphisms of the prion protein gene (PRNP) in a Korean population

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Iatrogenic Creutzfeldt-Jakob disease from commercial cadaveric human growth hormone.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Dura mater graft-associated Creutzfeldt-Jakob disease in Japan: clinicopathological and molecular characterization of the two distinct subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

The first Japanese patient with variant Creutzfeldt-Jakob disease (vCJD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

Human prion protein with valine 129 prevents expression of variant CJD phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

Prion disease with octapeptide repeat insertion.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4890484

High incidence of genetic human transmissible spongiform encephalopathies in Italy

28 November 2018

1 reference

12 December 2020

The first Japanese case of variant Creutzfeldt-Jakob disease showing periodic electroencephalogram

1 reference

12 December 2020

1 reference

12 December 2020

Variant Creutzfeldt-Jakob disease

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

Distribution of codon 129 genotype in human growth hormone-treated CJD patients in France and the UK

1 reference

12 December 2020

Human prion diseases: cause, clinical and diagnostic aspects

1 reference

12 December 2020

Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

Putative neurosurgical transmission of Creutzfeldt-Jakob disease with analysis of donor and recipient: agent strains

1 reference

12 December 2020

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

Prevention of iatrogenic transmission of Creutzfeldt-Jakob disease

1 reference

12 December 2020

Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population

1 reference

12 December 2020

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

1 reference

12 December 2020

Variant Creutzfeldt-Jakob disease in Hong Kong

1 reference

12 December 2020

Variant CJD in an individual heterozygous for PRNP codon 129

1 reference

12 December 2020

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

1 reference

https://api.crossref.org/works/10.1186%2FS40249-016-0143-8

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1186/S40249-016-0143-8

1 reference

Dimensions Publication ID

1017213346

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Fatcat ID

release_hpscmsoq45a2pctmo2273c6rm4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hpscmsoq45a2pctmo2273c6rm4

24 November 2022

mapped directly with Wikidata item

1 reference

1 reference

PubMed publication ID

27251305

1 reference