(Q45751552)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22288561%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22288561%20AND%20SRC:MED&resulttype=core&format=json

Creutzfeldt-Jakob disease

21 January 2020

main subject

prion protein family

0 references

1 reference

3

1 reference

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21 January 2020

Fabio Moda

1

1 reference

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21 January 2020

Antonio Indaco

4

1 reference

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21 January 2020

Pietro Zerbi

12

1 reference

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21 January 2020

Jean C Manson

16

1 reference

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21 January 2020

Fabrizio Tagliavini

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22288561%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Giorgio Giaccone

17

1 reference

ORCID Public Data File 2021

Silvia Suardi

2

object named as

Silvia Suardi

1 reference

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21 January 2020

8

Ilaria Campagnani

1 reference

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21 January 2020

5

Lucia Limido

1 reference

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21 January 2020

9

Jan Langeveld

1 reference

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21 January 2020

7

Margherita Ruggerone

1 reference

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21 January 2020

6

Chiara Vimercati

1 reference

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21 January 2020

13

Paolo Fociani

1 reference

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21 January 2020

15

Robert G Will

1 reference

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21 January 2020

author name string

Alessandro Terruzzi

10

1 reference

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21 January 2020

Antonio Brambilla

11

1 reference

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21 January 2020

Matthew T Bishop

14

1 reference

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21 January 2020

publication date

21 February 2012

1 reference

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21 January 2020

1 reference

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21 January 2020

volume

22

1 reference

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21 January 2020

issue

5

1 reference

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21 January 2020

page(s)

662-669

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22288561%20AND%20SRC:MED&resulttype=core&format=json

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

21 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Iatrogenic Creutzfeldt-Jakob disease: the waning of an era.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

The sequential development of the brain lesion of scrapie in three strains of mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Sporadic and familial CJD: classification and characterisation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Molecular biology and pathology of prion strains in sporadic human prion diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Prion protein conformation in a patient with sporadic fatal insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Familial and sporadic fatal insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

A subtype of sporadic prion disease mimicking fatal familial insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Genetic influence on the structural variations of the abnormal prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Sporadic fatal insomnia with spongiform degeneration in the thalamus and widespread PrPSc deposits in the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

Coexistence of multiple PrPSc types in individuals with Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2012.00572.X

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/10.1111%2FJ.1750-3639.2012.00572.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/10.1111%2FJ.1750-3639.2012.00572.X