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

Amaurosis fugax caused by hereditary thrombophilia due to mutation of gene.

Bratislavske lekarske listy - 1 Jan 2009

Titlic M, Bradic-Hammoud M, Miric L

Abstract excerpt

We are presenting a 59-year-old woman and 37-year-old man with amaurosis fugax. They underwent a comprehensive ophthalmological and neurological examination. Standard diagnostic examination revealed no possible cause of this temporary condition, therefore additional genetic analysis for possible hereditary thrombophilia was performed. Examination established hereditary thrombophilia: the heterozygotic type gene...

Read the complete abstract on PubMed

Topics

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

Share to ACE gene
Share to MTHFR gene
Share to PDF gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Plasminogen Activator Inhibitor 1

Share to Thrombophilia

Source

Identifiers

PMID: 19507653

Genes

ACE
MTHFR
PDF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Amaurosis fugax caused by hereditary thrombophilia due to mutation of gene.PMID 19507653Read ↗

Amaurosis fugax: associations with heritable thrombophilia.Semantic proximity Read ↗

Anterior ischemic optic neuropathy comorbid with Factor V Leiden and PAI-1 4G/5G mutation.Semantic proximity Read ↗

Cilioretinal artery: Vasculogenesis might be promoted by plasminogen activator inhibitor-1 5G allele.Semantic proximity Read ↗

NONICHEMIC CENTRAL RETINAL VEIN OCCLUSION ASSOCIATED WITH HEREDITARY THROMBOPHYLIA.Semantic proximity Read ↗

Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control study.Semantic proximity Read ↗

[Amaurosis fugax in Marfan syndrome with myxomatous degeneration].Semantic proximity Read ↗

Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion.Semantic proximity Read ↗

Venous thromboembolism does not share familial susceptibility with retinal vascular occlusion or glaucoma: a nationwide family study.Semantic proximity Read ↗

Thrombophilic gene mutations in children with migraine.Semantic proximity Read ↗

Transient ischemic attacks in a child with post-varicella arteriopathy and MTHFR homozigotic mutation C677T.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase polymorphisms as risk factors for retinal venous occlusive disease: A literature review.Semantic proximity Read ↗

Hyperbaric oxygen treatment results in a group of Turkish central retinal artery occlusion patients with a combined presence of thrombophilic mutations.Semantic proximity Read ↗

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