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

[Cerebral venous thrombosis in a girl carrier of the prothrombin gene mutation 20210G--> A treated by local fibrinolysis of the superior sagittal sinus].

Revista de neurologia - 1 Jan 2000

Perez- Dueñas B, Cambra- Lasaosa F J, Noguera-Julián A, Palomeque-Rico A, Toll-Costa T, Campistol J, Guimaraens-Martínez L, Vivas-Díaz E

Abstract excerpt

CASE REPORT: Girl, aged 4, without antecedents who was admitted to our hospital for drowsiness and progressive sensorial depression. Within 24 hours the clinical picture deteriorated with partial seizures of the right hand side of the body and right hemiparesis. A brain CAT scan showed a left temporoparietal parenchymatous haematoma with collapse of the left lateral ventricle and moderate obliteration of the...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to CAT gene

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutation

Share to Plasminogen Activators

Share to Prothrombin

Share to Urokinase-Type Plasminogen Activator

Source

Identifiers

PMID: 12436395

Genes

CAT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Cerebral venous thrombosis in a girl carrier of the prothrombin gene mutation 20210G--> A treated by local fibrinolysis of the superior sagittal sinus].PMID 12436395Read ↗

[Factor V Leiden mutation as a cause of venous thrombosis].Semantic proximity Read ↗

[Cerebral and systemic venous thrombosis associated to prothrombin G20210 mutation: case report].Semantic proximity Read ↗

Superior sagittal sinus thrombosis in a patient heterozygous for the novel 20210 A allele of the prothrombin gene.Semantic proximity Read ↗

[Cerebral sinovenous thrombosis in a newborn with mutation of MTHFR C677T treated with enoxaparin].Semantic proximity Read ↗

Prothrombin gene variant (G20210A) in a patient with cerebral venous sinus thrombosis.Semantic proximity Read ↗

An unusual cause of cerebral venous sinus thrombosis: prothrombin G20210A gene mutation.Semantic proximity Read ↗

Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study.Semantic proximity Read ↗

Role of genetic prothrombotic risk factors in childhood caval vein thrombosis.Semantic proximity Read ↗

Thrombosis of the deep cerebral veins with excessive bilateral infarction in a premature infant with the thrombogenic 4G/4G genotype of the plasminogen activator inhibitor-1.Semantic proximity Read ↗

Prothrombotic risk factors in childhood stroke and venous thrombosis.Semantic proximity Read ↗

High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives.Semantic proximity Read ↗

[Primary antiphospholipid syndrome in combination with heterozygous mutation in prothrombin (G20210A) gene: a case report].Semantic proximity Read ↗

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