Le syndrome de Blau = Blau syndromeMICELI-RICHARD, Corinne; RYBOJAD, Michel.Revue du rhumatisme monographies (Print). 2011, Vol 78, Num 3, pp 210-214, issn 1878-6227, 5 p.Article

The NOD2 Defect in Blau Syndrome Does Not Result in Excess Interleukin-1 ActivityMARTIN, Tammy M; ZILI ZHANG; KURZ, Paul et al.Arthritis and rheumatism. 2009, Vol 60, Num 2, pp 611-618, issn 0004-3591, 8 p.Article

A new CARD15 mutation in Blau syndromeVAN DUIST, Marjan M; ALBRECHT, Mario; PODSWIADEK, Marta et al.European journal of human genetics. 2005, Vol 13, Num 6, pp 742-747, issn 1018-4813, 6 p.Article

Blau syndromeMARTIN, J; KODJIKIAN, L; DUQUESNE, A et al.QJM (Oxford. 1994. Print). 2011, Vol 104, Num 11, pp 997-998, issn 1460-2725, 2 p.Article

Leg ulcers : A new symptom of Blau syndrome?DHONDT, Veerle; HOFMAN, Sarah; DAHAN, Karin et al.EJD. European journal of dermatology. 2008, Vol 18, Num 6, pp 635-637, issn 1167-1122, 3 p.Article

Blau syndrome presenting with ichthyosisMASEL, Grant; HALBERT, Anne.Australasian journal of dermatology. 2005, Vol 46, Num 1, pp 29-32, issn 0004-8380, 4 p.Article

Widespread granulomatous dermatitis of infancy : An early sign of blau syndromeSCHAFFER, Julie V; CHANDRA, Pranil; KEEGAN, Brian R et al.Archives of dermatology (1960). 2007, Vol 143, Num 3, pp 386-391, issn 0003-987X, 6 p.Article

A sporadic case of early-onset sarcoidosis resembling Blau syndrome due to the recurrent R334W missense mutation on the NOD2 geneCOTO-SEGURA, P; MALLO-GARCIA, S; COSTA-ROMERO, M et al.British journal of dermatology (1951). 2007, Vol 157, Num 6, pp 1257-1259, issn 0007-0963, 3 p.Article

Blau syndrome associated with a CARD15/NOD2 mutationSNYERS, Bernadette; DAHAN, Karin.American journal of ophthalmology. 2006, Vol 142, Num 6, pp 1089-1092, issn 0002-9394, 4 p.Article

Role of the NOD2 Genotype in the Clinical Phenotype of Blau Syndrome and Early-Onset SarcoidosisOKAFUJI, Ikuo; NISHIKOMORI, Ryuta; TANIZAKI, Hideaki et al.Arthritis and rheumatism. 2009, Vol 60, Num 1, pp 242-250, issn 0004-3591, 9 p.Article

Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutationKUROKAWA, Toru; KIKUCHI, Takanobu; OHTA, Kouichi et al.Ophthalmology (Rochester, MN). 2003, Vol 110, Num 10, pp 2040-2044, issn 0161-6420, 5 p.Article

Sporadic Blau Syndrome With Onset of Widespread Granulomatous Dermatitis in the Newborn PeriodSTOEVESANDT, Johanna; MORBACH, Henner; MARTIN, Tammy M et al.Pediatric dermatology. 2010, Vol 27, Num 1, pp 69-73, issn 0736-8046, 5 p.Article

A novel mutation in the NOD2 gene associated with Blau syndrome : a Norwegian family with four affected membersMILMAN, N; URSIN, K; RØDEVAND, E et al.Scandinavian journal of rheumatology. 2009, Vol 38, Num 3, pp 190-197, issn 0300-9742, 8 p.Article

Blau syndrome: A new kindredALONSO, Delilah; ELGART, George W; SCHACHNER, Lawrence A et al.Journal of the American Academy of Dermatology. 2003, Vol 49, Num 2, pp 299-302, issn 0190-9622, 4 p.Article

Interstitial pneumonitis in blau syndrome with documented mutation in CARD15BECKER, Mara L; MARTIN, Tammy M; DOYLE, Trudy M et al.Arthritis and rheumatism. 2007, Vol 56, Num 4, pp 1292-1294, issn 0004-3591, 3 p.Article

NOD2 gene-associated pediatric granulomatous arthritis : Clinical diversity, novel and Recurrent Mutations, and Evidence of Clinical Improvement With Interleukin-1 Blockade in a Spanish CohortAROSTEGUI, Juan I; ARNAL, Cristina; RIUS, Josefa et al.Arthritis and rheumatism. 2007, Vol 56, Num 11, pp 3805-3813, issn 0004-3591, 9 p.Article

Favourable effect of TNF-α inhibitor (infliximab) on Blau syndrome in monozygotic twins with a de novo CARD15 mutationMILMAN, Nils; ANDERSEN, Claus B; HANSEN, Annette et al.APMIS. Acta pathologica, microbiologica et immunologica Scandinavica. 2006, Vol 114, Num 12, pp 912-919, issn 0903-4641, 8 p.Article

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD 15) geneKING, Kathy; BAGNALL, Richard; ROBERTS, Roland G et al.Genomics (San Diego, Calif.). 2007, Vol 90, Num 4, pp 493-501, issn 0888-7543, 9 p.Article

Analysis of CARD15 polymorphisms in Korean patients with ankylosing spondylitis reveals absence of common variants seen in western populationsKIM, Tae-Hwan; RAHMAN, Proton; JUN, Jae-Bum et al.Journal of rheumatology. 2004, Vol 31, Num 10, pp 1959-1961, issn 0315-162X, 3 p.Article

Thalidomide Dramatically Improves the Symptoms of Early-Onset Sarcoidosis/Blau Syndrome: Its Possible Action and MechanismYASUI, Kozo; YASHIRO, Masato; TSUGE, Mitsuru et al.Arthritis and rheumatism. 2010, Vol 62, Num 1, pp 250-257, issn 0004-3591, 8 p.Article

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-κB activation: common genetic etiology with Blau syndromeKANAZAWA, Nobuo; OKAFUJI, Ikuo; NAKAJIMA, Mitsuru et al.Blood. 2005, Vol 105, Num 3, pp 1195-1197, issn 0006-4971, 3 p.Article

Morphologic and immunohistochemical characterization of granulomas in the nucleotide oligomerization domain 2―related disorders Blau syndrome and Crohn diseaseJANSSEN, Carl E. I; ROSE, Carlos D; DESMET, Valeer J et al.Journal of allergy and clinical immunology. 2012, Vol 129, Num 4, pp 1076-1084, issn 0091-6749, 9 p.Article

NOD2-associated diseases: Bridging innate immunity and autoinflammationBORZUTZKY, Arturo; FRIED, Ari; CHOU, Janet et al.Clinical immunology (Orlando, Fla. Print). 2010, Vol 134, Num 3, pp 251-261, issn 1521-6616, 11 p.Article

Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritisROSE, CARLOS D; DOYLE, TRUDY M; MCILVAIN-SIMPSON, GAIL et al.Journal of rheumatology. 2005, Vol 32, Num 2, pp 373-375, issn 0315-162X, 3 p.Article