(Q30698122)

26 June 2017

1 reference

title

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

1 reference

26 June 2017

0 references

1

Inga Zerr

1 reference

26 June 2017

Sigrid Poser

2

1 reference

26 June 2017

1 January 2002

1 reference

Acta Pathologica et Microbiologica Scandinavica

26 June 2017

1 reference

26 June 2017

110

1 reference

26 June 2017

1

1 reference

26 June 2017

88-98

1 reference

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

26 June 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Molecular genetics of human prion diseases in Germany.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

The pulvinar sign on magnetic resonance imaging in variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

New variant Creutzfeldt-Jakob disease: psychiatric features

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Creutzfeldt-Jacob disease associated with the PRNP codon 200Lys mutation: an analysis of 45 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Mutations and polymorphisms in the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

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/10.1034%2FJ.1600-0463.2002.100111.X

Diagnosis of new variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

High levels of nervous system-specific proteins in cerebrospinal fluid in patients with early stage Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

14-3-3 protein cerebrospinal fluid detection in human growth hormone-treated Creutzfeldt-Jakob disease patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Use of 14-3-3 and other brain-specific proteins in CSF in the diagnosis of variant Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

How to improve the clinical diagnosis of Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Hashimoto's encephalitis as a differential diagnosis of Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Iatrogenic Creutzfeldt-Jakob disease at the millennium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

CSF detection of the 14-3-3 protein in unselected patients with dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

Variant Creutzfeldt-Jakob disease in an elderly patient

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

Abnormal proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

Decreased beta-amyloid1-42 in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

Dementia with Lewy bodies in a neuropathologic series of suspected Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0463.2002.100111.X

7 January 2021

10.1034/J.1600-0463.2002.100111.X

Identifiers

DOI

1 reference

26 June 2017

1 reference

PubMed ID

12064260