(Q36647882)

15 August 2017

Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease (English)

1 reference

15 August 2017

1 reference

L Cervenáková

1

1 reference

15 August 2017

L G Goldfarb

2

1 reference

15 August 2017

R Garruto

3

1 reference

15 August 2017

H S Lee

4

1 reference

15 August 2017

D C Gajdusek

5

1 reference

15 August 2017

P Brown

6

1 reference

15 August 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

Proceedings of the National Academy of Sciences of the United States of America

15 August 2017

1 reference

15 August 2017

95

1 reference

15 August 2017

22

1 reference

15 August 2017

13239-13241

1 reference

Pathology and immunocytochemistry of a kuru brain

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

Is the neuropathology of new variant Creutzfeldt-Jakob disease and kuru similar?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

Comparative neuropathology of Kuru with the new variant of Creutzfeldt-Jakob disease: evidence for strain of agent predominating over genotype of host.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23768

New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests

20 September 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13239

Codon 129 genotype and new variant CJD

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13239

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13239

Genotype at codon 129 and susceptibility to Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13239

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789072

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.95.22.13239

1 reference

15 August 2017

0 references

1 reference

15 August 2017

1 reference