Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Neurology - 28 Sept 2010

Mateen F J, Krecke K, Younge B R, Ford A L, Shaikh A, Kothari P H, Atkinson J P

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain Diseases
Share to Diffusion Magnetic Resonance Imaging
Share to Exodeoxyribonucleases
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Phosphoproteins

Share to Retinal Diseases

Share to Retinal Vessels

Source

Open in PubMed Open full text

Identifiers

PMID: 20876473
DOI: 10.1212/WNL.0b013e3181f4d7ac
PMCID: PMC3013489

Genes

TREX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evolution of a tumor-like lesion in cerebroretinal vasculopathy and TREX1 mutation.PMID 20876473Read ↗

Novel de novo TREX1 mutation in a patient with retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations mimicking demyelinating disease.Semantic proximity Read ↗

Retinal vasculopathy with cerebral leukoencephalopathy due to TREX-1 mutation: An important mimicker of CNS inflammatory disease.Semantic proximity Read ↗

Cerebroretinal microangiopathy with calcifications and cysts: A case report.Semantic proximity Read ↗

Neuroimaging Findings in Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic Manifestations.Semantic proximity Read ↗

[Retinal vasculopathy with cerebral leukoencephalopathy carrying TREX1 mutation diagnosed by the intracranial calcification: a case report].Semantic proximity Read ↗

Neuropathology and Genetics of Cerebroretinal VasculopathiesSemantic proximity Read ↗

Pictorial essay of Werdnig-Hoffman disease.Semantic proximity Read ↗

First case of TREX1 mutation-driven retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations coexisting with lupus nephritis: a case report and mechanistic discussion.Semantic proximity Read ↗

TREX1 C-terminal frameshift mutations in the systemic variant of retinal vasculopathy with cerebral leukodystrophySemantic proximity Read ↗

A TREX1 mutation causing cerebral vasculopathy in a patient with familial chilblain lupus.Semantic proximity Read ↗

Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations in conjunction with systemic lupus erythematosus: Missed diagnosis or misdiagnosis?Semantic proximity Read ↗

Retinopathy With Multiple Cerebral Ring-Enhancing Lesions in a Young Man.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.