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

Blau syndrome revisited.

Current opinion in rheumatology - 1 Sept 2011

Rose Carlos D, Martin Tammy M, Wouters Carine H

Abstract excerpt

PURPOSE OF REVIEW: Blau syndrome is a monogenic disease resulting from mutations in nucleotide oligomerization domain 2 (NOD2) and is phenotypically characterized by granulomatous polyarthritis and uveitis. Not only there has been significant progress in disease characterization but also the biological pathways associated with NOD2 and related proteins of the innate immunity are better understood. RECENT...

Read the complete abstract on PubMed

Topics

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

Share to Arthritis
Share to Ligands
Share to Nod2 Signaling Adaptor Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sarcoidosis

Share to Syndrome

Share to Synovitis

Share to Terminology as Topic

Share to Uveitis

Source

Identifiers

PMID: 21788900
DOI: 10.1097/BOR.0b013e328349c430

Genes

NOD2

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

Blau syndrome revisited.PMID 21788900Read ↗

Blau syndrome, the prototypic auto-inflammatory granulomatous disease.Semantic proximity Read ↗

Blau syndrome-associated uveitis and the NOD2 gene.Semantic proximity Read ↗

A Novel Pathogenic NOD2 Variant in a Mother and Daughter with Blau Syndrome.Semantic proximity Read ↗

With a mere nod, uveitis enters a new era.Semantic proximity Read ↗

Blau Syndrome: NOD2-related systemic autoinflammatory granulomatosis.Semantic proximity Read ↗

A novel mutation in the<i>NOD2</i>gene associated with Blau syndrome: a Norwegian family with four affected membersSemantic proximity Read ↗

A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.Semantic proximity Read ↗

NOD2-Related Multisystem Inflammatory Disorders and Recent Advances.Semantic proximity Read ↗

Ocular manifestations of Blau syndrome.Semantic proximity Read ↗

Retinal Vasculitis in Familial Blau Syndrome.Semantic proximity Read ↗

Distinguishing Blau Syndrome from Systemic Sarcoidosis.Semantic proximity Read ↗

Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome.Semantic proximity Read ↗

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