(Q48474253)

11 February 2018

title

Increased incidence of sporadic Creutzfeldt-Jakob disease in the age groups between 70 and 90 years in Belgium (English)

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11 February 2018

sporadic Creutzfeldt-Jakob disease

main subject

Belgium

0 references

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Van Everbroeck B

1

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11 February 2018

Michotte A

2

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Sciot R

3

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11 February 2018

Godfraind C

4

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11 February 2018

Deprez M

5

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11 February 2018

Quoilin S

6

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11 February 2018

Martin JJ

7

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11 February 2018

Cras P

8

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11 February 2018

publication date

12 July 2006

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11 February 2018

European Journal of Epidemiology

published in

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11 February 2018

volume

21

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11 February 2018

issue

6

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11 February 2018

page(s)

443-447

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11 February 2018

Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10654-006-9012-2

21 January 2018

Typing prion isoforms.

1 reference

12 December 2020

Laboratory diagnosis of variant Creutzfeldt-Jakob disease.

1 reference

12 December 2020

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system

1 reference

12 December 2020

Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering

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12 December 2020

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

Antigen retrieval in prion protein immunohistochemistry

1 reference

12 December 2020

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

1 reference

12 December 2020

Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients

1 reference

12 December 2020

A prospective study of CSF markers in 250 patients with possible Creutzfeldt-Jakob disease

1 reference

12 December 2020

Phenotypic variability in familial prion diseases due to the D178N mutation.

1 reference

12 December 2020

The same prion strain causes vCJD and BSE

1 reference

12 December 2020

Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype

1 reference

12 December 2020

Neuropathological phenotype and ‘prion protein’ genotype correlation in sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

Decreased Levels of Amyloid-beta 1-42 in Cerebrospinal Fluid of Creutzfeldt-Jakob Disease Patients

1 reference

12 December 2020

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Phosphorylated tau in cerebrospinal fluid as a marker for Creutzfeldt-Jakob disease

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

Retrospective study of Creutzfeldt-Jakob disease in Belgium: neuropathological findings

1 reference

12 December 2020

Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt–Jakob disease

1 reference

12 December 2020

Epidemiology and risk factors of transmissible spongiform encephalopathies in man.

1 reference

12 December 2020

A retrospective study of Creutzfeldt-Jakob disease in Belgium

1 reference

12 December 2020

10.1007/S10654-006-9012-2

Identifiers

DOI

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11 February 2018

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11 February 2018