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

Successful management of hereditary angioedema during pregnancy in a patient with heterozygous MTHFR mutation.

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology - 1 Jun 2017

Martinez Saguer Inmaculada, Escuriola Ettingshausen Carmen

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 Anticoagulants
Share to Complement C1 Inhibitor Protein
Share to MTHFR gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Pregnancy

Share to Pregnancy Complications

Share to Thrombosis

Source

Identifiers

PMID: 28465053
DOI: 10.1016/j.anai.2017.04.001

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Successful management of hereditary angioedema during pregnancy in a patient with heterozygous MTHFR mutation.PMID 28465053Read ↗

Management of hereditary angioedema type I and homozygous MTHFR mutation during pregnancy.Semantic proximity Read ↗

Management of hereditary angioedema in pregnant women: a reviewSemantic proximity Read ↗

Hereditary angioedema in women: specific challenges.Semantic proximity Read ↗

Thrombotic Microangiopathy in Pregnancy: Current Understanding and Management StrategiesSemantic proximity Read ↗

International Consensus on the Use of Genetics in the Management of Hereditary AngioedemaSemantic proximity Read ↗

Repeated attacks of type III hereditary angioedema with factor XII mutation during pregnancy.Semantic proximity Read ↗

Genotype-guided medical treatment of arteriovenous malformation.Semantic proximity Read ↗

Recognizing and managing hereditary angioedema.Semantic proximity Read ↗

Postpartum atypical hemolytic uremic syndrome with complement factor H mutation complicated by reversible cerebrovascular constriction syndrome successfully treated with eculizumab.Semantic proximity Read ↗

Hereditary angioedema: the clinical syndrome and its management in the United States.Semantic proximity Read ↗

Type 1 hereditary angioedema in a 72-year-old woman.Semantic proximity Read ↗

Management of brothers with haemophilia A and familial cerebral cavernous malformations.Semantic proximity Read ↗

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