Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects (Q30467870)

11 August 2017

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

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11 August 2017

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11

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PubMed publication ID

22558438

21 June 2017

Cornelia M. van Duijn

15

Cornelia M van Duijn

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Carla Ibrahim-Verbaas

Carla A Ibrahim-Verbaas

4

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Marcel Verbeek

Marcel M Verbeek

10

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Piero Parchi

Piero Parchi

2

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Sabina Capellari

Sabina Capellari

3

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Maaike Schuur

5

Maaike Schuur

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11 August 2017

6

Rosaria Strammiello

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11 August 2017

9

Willem A van Gool

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11 August 2017

Annemieke J M Rozemuller

16

Annemieke J M Rozemuller

1 reference

11 August 2017

Casper Jansen

1

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11 August 2017

Patrizia Corrado

7

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11 August 2017

Matthew T Bishop

8

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11 August 2017

Wesley van Saane

12

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11 August 2017

Wim G M Spliet

13

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11 August 2017

Gerard H Jansen

14

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11 August 2017

language of work or name

English

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publication date

30 April 2012

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11 August 2017

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11 August 2017

7

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11 August 2017

4

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11 August 2017

e36333

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Creative Commons Attribution 4.0 International

11 August 2017

start time

30 April 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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20 June 2018

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20 June 2018

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20 June 2018

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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

20 June 2018

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

20 June 2018

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Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.

20 June 2018

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Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics

20 June 2018

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

20 June 2018

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Further characterisation of the prion protein molecular types detectable in the NIBSC Creutzfeldt-Jakob disease brain reference materials

20 June 2018

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Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease

20 June 2018

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A novel human disease with abnormal prion protein sensitive to protease

20 June 2018

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Beyond PrP9res) type 1/type 2 dichotomy in Creutzfeldt-Jakob disease

20 June 2018

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Insights into prion strains and neurotoxicity

20 June 2018

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The first case of variant Creutzfeldt-Jakob disease in The Netherlands

20 June 2018

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Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease

20 June 2018

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Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease

20 June 2018

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20 June 2018

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Early cognitive decline is associated with prion protein codon 129 polymorphism

20 June 2018

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20 June 2018

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Creutzfeldt-Jakob disease 38 years after diagnostic use of human growth hormone

20 June 2018

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Iatrogenic Creutzfeldt-Jakob disease at the millennium.

20 June 2018

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20 June 2018

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20 June 2018

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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

20 June 2018

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

20 June 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

20 June 2018

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20 June 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology

21 January 2018

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The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

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

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

Classification of sporadic Creutzfeldt-Jakob disease revisited.

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

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

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0036333

Immunohistochemistry for the prion protein: comparison of different monoclonal antibodies in human prion disease subtypes.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340342

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3340342

Genotyping of the prion protein gene at codon 129

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22558438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22558438

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0036333

1 reference

11 August 2017

0 references

1 reference

11 August 2017

PubMed publication ID

22558438

1 reference