Genetic prion disease: the EUROCJD experience. (Q48532612)

12 February 2018

title

Genetic prion disease: the EUROCJD experience. (English)

1 reference

12 February 2018

0 references

1

1 reference

12 February 2018

Maurizio Pocchiari

4

1 reference

12 February 2018

Herbert Budka

5

1 reference

12 February 2018

Adriano Aguzzi

18

1 reference

12 February 2018

Maria Puopolo

Maria Puopolo

2

0 references

Cornelia M. van Duijn

6

Cornelia van Duijn

1 reference

12 February 2018

13

Inga Zerr

1 reference

12 February 2018

Richard S. G. Knight

20

Richard Knight

1 reference

12 February 2018

Robert G. Will

22

Robert Will

1 reference

12 February 2018

author name string

Anna Ladogana

3

1 reference

12 February 2018

Steven J Collins

7

1 reference

12 February 2018

Alison Boyd

8

1 reference

12 February 2018

Antonio Giulivi

9

1 reference

12 February 2018

Mike Coulthart

10

1 reference

12 February 2018

Nicole Delasnerie-Laupretre

11

1 reference

12 February 2018

Jean Philippe Brandel

12

1 reference

12 February 2018

Hans A Kretzschmar

14

1 reference

12 February 2018

Jesus de Pedro-Cuesta

15

1 reference

12 February 2018

Miguel Calero-Lara

16

1 reference

12 February 2018

Markus Glatzel

17

1 reference

12 February 2018

Matthew Bishop

19

1 reference

12 February 2018

Girma Belay

21

1 reference

12 February 2018

Eva Mitrova

23

1 reference

12 February 2018

EUROCJD

24

1 reference

12 February 2018

publication date

15 November 2005

1 reference

12 February 2018

published in

Human Genetics

1 reference

12 February 2018

volume

118

1 reference

12 February 2018

issue

2

1 reference

12 February 2018

page(s)

166-174

1 reference

12 February 2018

https://scigraph.springernature.com/pub.10.1007/s00439-005-0020-1

exact match

0 references

cites work

The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-005-0020-1

Descriptive epidemiology of Creutzfeldt-Jakob disease in Chile

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-005-0020-1

Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brain

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-005-0020-1

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy

21 January 2018

1 reference

12 December 2020

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

1 reference

12 December 2020

Cluster of Creutzfeldt-Jakob disease and presenile dementia

1 reference

12 December 2020

Prion disease with octapeptide repeat insertion.

1 reference

12 December 2020

Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 Patients dying during the decade 1968-1977

1 reference

12 December 2020

Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents

1 reference

12 December 2020

High incidence of genetic human transmissible spongiform encephalopathies in Italy

1 reference

12 December 2020

Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

"Clusters" of CJD in Slovakia: the first statistically significant temporo-spatial accumulations of rural cases

1 reference

12 December 2020

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

1 reference

12 December 2020

Creutzfeldt-Jakob disease and stress

1 reference

12 December 2020

When sporadic disease is not sporadic: the potential for genetic etiology

1 reference

12 December 2020

Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases).

1 reference

12 December 2020

Shattuck lecture--neurodegenerative diseases and prions

1 reference

12 December 2020

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

1 reference

12 December 2020

A prion-linked psychiatric disorder.

1 reference

12 December 2020

Mutations of the prion protein gene phenotypic spectrum

1 reference

12 December 2020

Creutzfeldt-Jakob Disease: Focus among Libyan Jews in Israel

1 reference

12 December 2020

Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

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

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

1 reference

12 December 2020

First experimental transmission of fatal familial insomnia.

1 reference

12 December 2020

Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

1 reference

12 December 2020

Genetic epidemiology of Creutzfeldt-Jakob disease in Europe

1 reference

12 December 2020

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river.

1 reference

12 December 2020

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

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

Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease

1 reference

12 December 2020

10.1007/S00439-005-0020-1

Identifiers

DOI

1 reference

12 February 2018

PubMed ID

16187142

1 reference

12 February 2018