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

The factor V G1691A mutation is a risk for porencephaly: A case-control study.

Annals of neurology - 1 Aug 2004

Debus Otfried M, Kosch Andrea, Sträter Ronald, Rossi Rainer, Nowak-Göttl Ulrike

Abstract excerpt

This study was initiated to investigate prothrombotic risk factors in children with porencephaly. 76 porencephalic and 76 healthy infants were investigated for factor V (FV) G1691A mutation, factor II G20210A variant, methylenetetrahydrofolate reductase (MTHFR) C677T genotype, lipoprotein (a), pr...

Read the complete abstract on PubMed

Topics

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

Share to Alanine
Share to Brain Diseases
Share to Chi-Square Distribution

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor V

Share to Glycine

Share to Multivariate Analysis

Share to Prothrombin

Source

Identifiers

PMID: 15293282
DOI: 10.1002/ana.20184

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15293282-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

The factor V G1691A mutation is a risk for porencephaly: A case-control study.PMID 15293282Read ↗

Factor V Leiden and genetic defects of thrombophilia in childhood porencephalySemantic proximity Read ↗

A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?Semantic proximity Read ↗

Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.Semantic proximity Read ↗

Genetic variants of the vitamin K dependent coagulation system and intraventricular hemorrhage in preterm infants.Semantic proximity Read ↗

The role of genetic factors in the pathogenesis of neonatal intraventricular hemorrhage.Semantic proximity Read ↗

Neonatal porencephaly and adult stroke related to mutations in collagen IV A1.Semantic proximity Read ↗

COL4A1 mutation in two preterm siblings with antenatal onset of parenchymal hemorrhage.Semantic proximity Read ↗

Increased prevalence of factor V Leiden mutation in premature but not in full-term infants with grade I intracranial haemorrhage.Semantic proximity Read ↗

Leiden V factor and spastic cerebral palsy in Mexican children.Semantic proximity Read ↗

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