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

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century

1 Jan 2003

Abstract excerpt

Hereditary haemorrhagic telangiectasia (HHT) affects one in 5-8000, and no longer can be viewed as solely causing anaemia (due to nasal and gastrointestinal bleeding) and characteristic mucocutaneous telangiectasia. Arteriovenous malformations commonly occur, and in the pulmonary and cerebral circulations demand knowledge of risks and benefits of asymptomatic screening and treatment. HHT is inherited as an...

Read the complete abstract on PubMed

Topics

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

Share to Tracheal and airway disorders
Share to Vascular Anomalies and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12566546
DOI: 10.1136/pmj.79.927.18

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st centuryPMID 12566546Read ↗

Hereditary haemorrhagic telangiectasia.Semantic proximity Read ↗

Hereditary haemorrhagic telangiectasia: a clinical and scientific review.Semantic proximity Read ↗

International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia.Semantic proximity Read ↗

Pulmonary hypertension associated with hereditary haemorrhagic telangiectasia: from genetics to clinical management.Semantic proximity Read ↗

Molecular defects in rare bleeding disorders: hereditary haemorrhagic telangiectasia.Semantic proximity Read ↗

Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations: issues in clinical management and review of pathogenic mechanisms.Semantic proximity Read ↗

Hereditary Haemorrhagic Telangiectasia, an Inherited Vascular Disorder in Need of Improved Evidence-Based Pharmaceutical Interventions.Semantic proximity Read ↗

European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)Semantic proximity Read ↗

Updates on diagnostic criteria for hereditary haemorrhagic telangiectasia in the light of whole genome sequencing of 'gene-negative' individuals recruited to the 100 000 Genomes Project.Semantic proximity Read ↗

Experience of the Irish National Centre for hereditary haemorrhagic telangiectasia 2003-2008.Semantic proximity Read ↗

Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures.Semantic proximity Read ↗

Pulmonary Arterial Hypertension and Hereditary Haemorrhagic TelangiectasiaSemantic proximity Read ↗

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