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Article

Prothrombotic factors in neonates with cerebral thrombosis and intraventricular hemorrhage.

Acta paediatrica (Oslo, Norway : 1992). Supplement - 1 Jan 2002

Aronis S, Bouza H, Pergantou H, Kapsimalis Z, Platokouki H, Xanthou M

Abstract excerpt

AIM: To investigate whether the factor V Leiden mutation (FVL), the prothrombin gene G20210A variant or the methylenetetrahydrofolate reductase (MTHFR) C677T genotype are risk factors for central nervous system (CNS) thrombosis or intraventricular hemorrhage (IVH) in neonates. METHODS: Thirteen full-term infants with cerebral infarct documented with magnetic resonance imaging were assessed with the whole spectrum...

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Source

Identifiers

PMID: 12477269
DOI: 10.1111/j.1651-2227.2002.tb02910.x

Genes

MTHFR

Variants

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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.

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