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

Atypical haemolytic uraemic syndrome.

British medical bulletin - 1 Jan 2006

Kavanagh David, Goodship Timothy H J, Richards Anna

Abstract excerpt

The haemolytic uraemic syndrome (HUS) is characterized by the triad of thrombocytopenia, microangiopathic haemolytic anaemia and acute renal failure. HUS may be classified as either diarrhoeal-associated or non-diarrhoeal/atypical (aHUS). aHUS has recently been shown to be a disease of complement...

Read the complete abstract on PubMed

Topics

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

Share to Complement Factor H
Share to Complement system in diseases
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to CFH gene

Share to Hemolytic-Uremic Syndrome

Share to Membrane Cofactor Protein

Share to Mutation

Share to Purpura, Thrombotic Thrombocytopenic

Source

Identifiers

PMID: 16968692
DOI: 10.1093/bmb/ldl004

Genes

CFH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16968692-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Atypical haemolytic uraemic syndrome.PMID 16968692Read ↗

Atypical hemolytic uremic syndrome: update on the complement system and what is new.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome.Semantic proximity Read ↗

[Atypical HUS caused by complement-related abnormalities].Semantic proximity Read ↗

Advances in understanding the aetiology of atypical Haemolytic Uraemic Syndrome.Semantic proximity Read ↗

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Atypical haemolytic uraemic syndrome: a case of rare genetic mutation.Semantic proximity Read ↗

An update for atypical haemolytic uraemic syndrome: Diagnosis and treatment. A consensus documentSemantic proximity Read ↗

[Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].Semantic proximity Read ↗

Atypical haemolytic uraemic syndrome and mutations in complement regulator genes.Semantic proximity Read ↗

Atypical hemolytic uremic syndrome, genetic basis, and clinical manifestations.Semantic proximity Read ↗

Atypical Hemolytic Uremic SyndromeSemantic proximity Read ↗

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