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 role of genetic factors in the pathogenesis of neonatal intraventricular hemorrhage.

Folia neuropathologica - 1 Jan 2015

Szpecht D, Szymankiewicz M, Seremak-Mrozikiewicz A, Gadzinowski J

Abstract excerpt

Intraventricular hemorrhage (IVH) affects 15-20% of babies born before 32 weeks of pregnancy. Besides gestational age (below 32 weeks) there are a number of IVH risk factors. Increasing attention is being paid to genetic factors in the development of IVH. The authors discuss genetic factors (mutations of coagulation factors, gene polymorphisms in pro-inflammatory cytokines, mutation of type IV collagen gene,...

Read the complete abstract on PubMed

Topics

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

Share to Cerebral Hemorrhage
Share to Cerebrovascular Circulation
Share to Cytokines

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn

Share to Infant, Premature

Share to Mutation

Source

Identifiers

PMID: 25909869
DOI: 10.5114/fn.2015.49968

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The role of genetic factors in the pathogenesis of neonatal intraventricular hemorrhage.PMID 25909869Read ↗

Gene-environment interactions in severe intraventricular hemorrhage of preterm neonates.Semantic proximity Read ↗

Genetics of perinatal brain injury in the preterm infant.Semantic proximity Read ↗

Genes and environment in neonatal intraventricular hemorrhage.Semantic proximity Read ↗

Hemangioma-related gene polymorphisms in the pathogenesis of intraventricular hemorrhage in preterm infants.Semantic proximity Read ↗

The significance of polymorphisms in genes encoding Il-1β, Il-6, TNFα, and Il-1RN in the pathogenesis of intraventricular hemorrhage in preterm infants.Semantic proximity Read ↗

Germinal matrix hemorrhage: intraventricular hemorrhage in very-low-birth-weight infants: the independent role of inherited thrombophilia.Semantic proximity Read ↗

Role of endothelial nitric oxide synthase and endothelin-1 polymorphism genes with the pathogenesis of intraventricular hemorrhage in preterm infants.Semantic proximity Read ↗

Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates.Semantic proximity Read ↗

The role of FV 1691G>A, FII 20210G>A mutations and MTHFR 677C>T; 1298A>C and 103G>T FXIII gene polymorphisms in pathogenesis of intraventricular hemorrhage in infants born before 32 weeks of gestation.Semantic proximity Read ↗

Genetic Profiling of Idiopathic Antenatal Intracranial Haemorrhage: What We Know?Semantic proximity Read ↗

Role of Heritable and Environmental Contributions to the Development of Severe Intraventricular Hemorrhage in Very Preterm Infants: Results from a Multicenter Twins Cohort Study.Semantic proximity Read ↗

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

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