(Q42148793)

17 October 2017

Multiple sclerosis-like lesions and type I interferon signature in a patient with RVCL. (English)

1 reference

17 October 2017

0 references

1 reference

8

Tania Kümpfel

1 reference

17 October 2017

6

Min Ae Lee-Kirsch

1 reference

17 October 2017

Elisabeth Schuh

1

1 reference

17 October 2017

Birgit Ertl-Wagner

2

1 reference

17 October 2017

Peter Lohse

3

1 reference

17 October 2017

Waltraud Wolf

4

1 reference

17 October 2017

Johannes F Mann

5

1 reference

17 October 2017

Reinhard Hohlfeld

7

1 reference

17 October 2017

language of work or name

1 reference

23 December 2014

1 reference

Neurology(R) neuroimmunology & neuroinflammation

17 October 2017

1 reference

17 October 2017

2

1 reference

17 October 2017

1

1 reference

17 October 2017

e55

1 reference

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

17 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

Chronic exposure of astrocytes to interferon-α reveals molecular changes related to Aicardi-Goutieres syndrome

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

Evolution of a tumor-like lesion in cerebroretinal vasculopathy and TREX1 mutation

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

Cerebroretinal vasculopathy mimicking a brain tumor: a case of a rare hereditary syndrome

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4277301

10.1212/NXI.0000000000000055

17 August 2018

Identifiers

DOI

1 reference

17 October 2017

1 reference

17 October 2017

PubMed publication ID

25566545

1 reference