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

Neonatal antiphospholipid syndrome associated with heterozygous methylentetrahydrofolate reductase C677T and prothrombin G20210A gene mutations.

Rheumatology (Oxford, England) - 1 Apr 2007

Paro-Panjan D, Kitanovski L, Avcin T

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Antiphospholipid Syndrome
Share to Infant, Newborn
Share to Infarction, Middle Cerebral Artery
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Prothrombin

Source

Identifiers

PMID: 17307756
DOI: 10.1093/rheumatology/kem011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neonatal antiphospholipid syndrome associated with heterozygous methylentetrahydrofolate reductase C677T and prothrombin G20210A gene mutations.PMID 17307756Read ↗

Neonatal stroke associated with de novo antiphospholipid antibody and homozygous 1298C/C methylenetetrahydrofolate reductase mutation.Semantic proximity Read ↗

Heterozygous methylenetetrahydrofolate reductase 677C-T gene mutation with mild hyperhomocysteinemia associated with intrauterine iliofemoral artery thrombosis.Semantic proximity Read ↗

A child with Diamond-Blackfan anemia, methylenetetrahydrofolate reductase mutation, and perinatal stroke.Semantic proximity Read ↗

Maternal methylenetetrahydrofolate reductase (MTHFR) homozygosity and neonatal outcome: follow-up of 42 pregnancies at risk.Semantic proximity Read ↗

Renal vein thrombosis in a newborn with prothrombotic genetic risk factors.Semantic proximity Read ↗

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.Semantic proximity Read ↗

Livedo vasculopathy associated with methylenetetrahydrofolate reductase C677T homozygosity.Semantic proximity Read ↗

Neonatal sinovenous thrombosis associated with homozygous thermolabile methylenetetrahydrofolate reductase in both mother and infant.Semantic proximity Read ↗

Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene.Semantic proximity Read ↗

C 677T methylentetrahydrofolate reductase (MTHFR) polymorphism and thrombangiitis obliterans.Semantic proximity Read ↗

Homozygous Factor V Leiden mutation in a child with meningococcal purpura fulminans.Semantic proximity Read ↗

Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation.Semantic proximity Read ↗

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