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

Pediatric granulomatous arthritis: an international registry.

Arthritis and rheumatism - 1 Oct 2006

Rosé Carlos D, Wouters Carine H, Meiorin Silvia, Doyle Trudy M, Davey Michael P, Rosenbaum James T, Martin Tammy M

Abstract excerpt

OBJECTIVE: Blau syndrome and its sporadic counterpart, early-onset sarcoidosis, share an identical phenotype featuring the classic triad of arthritis, dermatitis, and uveitis and are associated with mutations of CARD15 in 50-90% of cases. We chose the term "pediatric granulomatous arthritis" to r...

Read the complete abstract on PubMed

Topics

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

Share to Arthritis
Share to Dermatitis
Share to Global Health

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nod2 Signaling Adaptor Protein

Share to Registries

Share to Sarcoidosis

Share to Syndrome

Share to Uveitis

Source

Identifiers

PMID: 17009307
DOI: 10.1002/art.22122

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17009307-2026-09-02.2. 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

Pediatric granulomatous arthritis: an international registry.PMID 17009307Read ↗

<i>NOD2</i> gene–associated pediatric granulomatous arthritis: Clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin‐1 blockade in a Spanish cohortSemantic proximity Read ↗

NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain.Semantic proximity Read ↗

Caveats and truths in genetic, clinical, autoimmune and autoinflammatory issues in Blau syndrome and early onset sarcoidosis.Semantic proximity Read ↗

Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis.Semantic proximity Read ↗

Review: Genetics and the Classification of Arthritis in Adults and Children.Semantic proximity Read ↗

Familial Granulomatous Uveitis with Arthritis Suggestive of Blau Syndrome: A Multigenerational Case Series from India.Semantic proximity Read ↗

Early-onset sarcoidosis caused by a rare CARD15/NOD2 de novo mutation and responsive to infliximab: a case report with long-term follow-up and review of the literature.Semantic proximity Read ↗

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome.Semantic proximity Read ↗

Widespread granulomatous dermatitis of infancy: an early sign of Blau syndrome.Semantic proximity Read ↗

Distinguishing Blau Syndrome from Systemic Sarcoidosis.Semantic proximity Read ↗

Blau syndrome of granulomatous arthritis, iritis, and skin rash: a new family and review of the literature.Semantic proximity Read ↗

[An era of international collaboration in pediatric rheumatology].Semantic proximity Read ↗

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