A Case of Blau Syndrome withNOD2E383K Mutation

Caveats and truths in genetic, clinical, autoimmune and autoinflammatory issues in Blau syndrome and early onset sarcoidosis

(2014) Francesco Caso et al.   AUTOIMMUNITY REVIEWS

Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes

(2014) C. D. Rose et al.   RHEUMATOLOGY

Mutational analysis of human NOD1 and NOD2 NACHT domains reveals different modes of activation

(2011) Birte Zurek et al.   Innate Immunity

Incomplete penetrance of theNOD2E383K substitution among members of a pediatric granulomatous arthritis pedigree

(2009) Frank T. Saulsbury et al.   ARTHRITIS AND RHEUMATISM

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

(2009) Carlos D. Rosé et al.   ARTHRITIS AND RHEUMATISM

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis

(2009) Ikuo Okafuji et al.   ARTHRITIS AND RHEUMATISM