(Q36957256)

17 August 2017

Human prion disease with a G114V mutation and epidemiological studies in a Chinese family: a case series (English)

1 reference

17 August 2017

0 references

3

Qi Shi

1 reference

17 August 2017

13

Xiao-Ping Dong

1 reference

17 August 2017

Jing Ye

1

1 reference

17 August 2017

Jun Han

2

1 reference

17 August 2017

Bao-Yun Zhang

4

1 reference

17 August 2017

Gui-Rong Wang

5

1 reference

17 August 2017

Chan Tian

6

1 reference

17 August 2017

Chen Gao

7

1 reference

17 August 2017

Jian-Min Chen

8

1 reference

17 August 2017

Cun-Jiang Li

9

1 reference

17 August 2017

Zheng Liu

10

1 reference

17 August 2017

Xian-Zhang Li

11

1 reference

17 August 2017

Lai-Zhong Zhang

12

1 reference

17 August 2017

language of work or name

English

0 references

publication date

17 October 2008

1 reference

Journal of Medical Case Reports

17 August 2017

1 reference

17 August 2017

2

1 reference

17 August 2017

331

1 reference

Clinical aspects of human spongiform encephalopathies, with the exception of iatrogenic forms

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2576332

Fatal familial insomnia: a new Austrian family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2576332

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2576332

Comparison study on clinical and neuropathological characteristics of hamsters inoculated with scrapie strain 263K in different challenging pathways

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2576332

Genetic predisposition to neurological symptoms in lacunar infarction

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1752-1947-2-331

[Familial prion disease (GSS, familial CJD, FFI)]

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18925969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Creutzfeldt-Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18925969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Characteristics of polymorphism of 129th amino acid in PRNP among Han and Uighur Chinese]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18925969

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1752-1947-2-331

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

18925969

1 reference