(Q36226900)

12 August 2017

0 references

Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene (English)

1 reference

12 August 2017

0 references

4

P L Lantos

1 reference

12 August 2017

T Kovács

1

1 reference

12 August 2017

J A Beck

2

1 reference

12 August 2017

M I Papp

3

1 reference

12 August 2017

Z Arányi

5

1 reference

12 August 2017

I G Szirmai

6

1 reference

12 August 2017

M Farsang

7

1 reference

12 August 2017

A Stuke

8

1 reference

12 August 2017

A Csillik

9

1 reference

12 August 2017

J Collinge

10

1 reference

12 August 2017

language of work or name

English

0 references

publication date

1 March 2007

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

12 August 2017

1 reference

12 August 2017

78

1 reference

12 August 2017

3

1 reference

12 August 2017

321-323

1 reference

Molecular neurology of prion disease

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Prion diseases of humans and animals: their causes and molecular basis

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

Prion disease with 144 base pair insertion in a Japanese family line

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117636

22 September 2018

Identifiers

DOI

10.1136/JNNP.2006.104372

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

17308293

1 reference