(Q42692446)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7902693%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease (English)

1 reference

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28 October 2019

0 references

1

1 reference

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28 October 2019

Mirella Salvatore

2

1 reference

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28 October 2019

Francesca Cutruzzola'

3

1 reference

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28 October 2019

Maurizio Genuardi

4

1 reference

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28 October 2019

author name string

Allocatelli CT

5

1 reference

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28 October 2019

Masullo C

6

1 reference

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28 October 2019

Macchi G

7

1 reference

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28 October 2019

Alemá G

8

1 reference

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28 October 2019

Galgani S

9

1 reference

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28 October 2019

Xi YG

10

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28 October 2019

publication date

1 December 1993

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28 October 2019

1 reference

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28 October 2019

volume

34

1 reference

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28 October 2019

page(s)

802-807

1 reference

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28 October 2019

issue

6

1 reference

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The scrapie agent and the prion hypothesis.

28 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twist

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

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/10.1002%2FANA.410340608

Creutzfeldt-Jakob disease in France: II. Clinical characteristics of 124 consecutive verified cases during the decade 1968-1977

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Identical mutation in unrelated patients with Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

A retrospective study of Creutzfeldt-Jakob disease in Italy (1972-1986).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

Creutzfeldt-Jakob disease after non-commercial dura mater graft

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FANA.410340608

21 January 2018

Identifiers

DOI

10.1002/ANA.410340608

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7902693%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference