NOD2-Associated pediatric granulomatous arthritis, an expanding phenotype: Study of an international registry and a national cohort in spain-Reference-Cited by-同舟云学术

NOD2-Associated pediatric granulomatous arthritis, an expanding phenotype: Study of an international registry and a national cohort in spain

Published:2009-06 Issue:6 Volume:60 Page:1797-1803
ISSN:0004-3591
Container-title:Arthritis & Rheumatism
language:en
Short-container-title:Arthritis Rheum

Author:

Rosé Carlos D.,Aróstegui Juan I.,Martin Tammy M.,Espada Graciela,Scalzi Lisabeth,Yagüe Jordi,Rosenbaum James T.,Modesto Consuelo,Cristina Arnal Maria,Merino Rosa,García-Consuegra Julia,Carballo Silva María Antonia,Wouters Carine H.

Publisher

Wiley

Subject

Pharmacology (medical),Immunology,Rheumatology,Immunology and Allergy

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2. Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis;Rose;J Rheumatol,2005

3. CARD15 mutations in Blau syndrome;Miceli-Richard;Nat Genet,2001

4. Familial granulomatous arthritis, iritis, and rash;Blau;J Pediatr,1985

5. Familial granulomatous synovitis, uveitis, and cranial neuropathies;Jabs;Am J Med,1985

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