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

Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis.

American journal of perinatology - 1 Sept 2016

Giuffrè Mario, Verso Clelia Lo, Serra Gregorio, Moceri Giovanni, Cimador Marcello, Corsello Giovanni

Abstract excerpt

Objective This report discusses the role of both congenital and acquired risk factors in the pathogenesis of portal vein thrombosis (PVT). Study Design We describe the clinical management and treatment of PVT in a preterm newborn with a homozygous mutation of the methylenetetrahydrofolate reductase (MTHFR) and plasminogen activator inhibitor-1 (PAI-1) genes and sepsis by Candida parapsilosis. Results Although...

Read the complete abstract on PubMed

Topics

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

Share to Anticoagulants
Share to Candidiasis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor V

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Plasminogen Activator Inhibitor 1

Share to Portal Vein

Share to Sepsis

Share to Venous Thrombosis

Source

Identifiers

PMID: 27603544
DOI: 10.1055/s-0036-1586102

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis.PMID 27603544Read ↗

Dual mutation (MTHFR A1298C with PAI (4G) mutation) manifesting with bilateral lower limb gangrene in a neonate.Semantic proximity Read ↗

Evaluation of Patients with Neonatal Thrombosis.Semantic proximity Read ↗

Association of prothrombin gene mutation with sepsis in a preterm with multiple intracardiac thrombi.Semantic proximity Read ↗

Abdominal venous thrombosis in neonates and infants: role of prothrombotic risk factors - a multicentre case-control study. For the Childhood Thrombophilia Study Group.Semantic proximity Read ↗

Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study.Semantic proximity Read ↗

Symptomatic thrombosis in Turkish neonates.Semantic proximity Read ↗

Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: a family study.Semantic proximity Read ↗

Prothrombotic factors in neonates with cerebral thrombosis and intraventricular hemorrhage.Semantic proximity Read ↗

Factor V Leiden and prothrombin gene 20210A variant in neonatal thromboembolism and in healthy neonates and adults: a study in a single center.Semantic proximity Read ↗

Sepsis-like cerebrovascular event in a newborn with MTHFR homozygous mutation.Semantic proximity Read ↗

Intraventricular hemorrhage in a full-term neonate associated with sinus venous thrombosis and homozygosity for the plasminogen activator inhibitor-1 4G/4G polymorphism.Semantic proximity Read ↗

Preterm infant with a catastrophic hemorrhagic-thromboembolic incident.Semantic proximity Read ↗

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