(Q37803365)

23 August 2017

Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis (English)

1 reference

Creutzfeldt-Jakob disease

23 August 2017

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fatal familial insomnia

1 reference

based on heuristic

inferred from title

1 reference

5

1 reference

23 August 2017

1

Sabina Capellari

1 reference

23 August 2017

3

Daniela Saverioni

1 reference

23 August 2017

2

Rosaria Strammiello

1 reference

23 August 2017

4

Hans Kretzschmar

1 reference

23 August 2017

27 October 2010

1 reference

23 August 2017

Acta Neuropathologica

1 reference

23 August 2017

121

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23 August 2017

1

1 reference

23 August 2017

21-37

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-010-0760-4

23 August 2017

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cites work

Demyelinating peripheral neuropathy with Creutzfeldt-Jakob disease and mutation at codon 200 of the prion protein gene.

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Clinical features of Creutzfeldt-Jakob disease with V180I mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Do Creutzfeldt-Jakob disease patients of Jewish Libyan origin have unique clinical features?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Molecular cloning of a human prion protein cDNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

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/10.1007%2FS00401-010-0760-4

Fatal familial insomnia: clinical and pathologic study of five new cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Inherited prion disease caused by the V210I mutation: transmission to transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

A subtype of sporadic prion disease mimicking fatal familial insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

Analysis of the prion protein gene in thalamic dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0760-4

10.1007/S00401-010-0760-4

21 January 2018

Identifiers

DOI

1 reference

23 August 2017

1 reference

PubMed ID

20978903