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4. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis. Okafuji I; Nishikomori R; Kanazawa N; Kambe N; Fujisawa A; Yamazaki S; Saito M; Yoshioka T; Kawai T; Sakai H; Tanizaki H; Heike T; Miyachi Y; Nakahata T Arthritis Rheum; 2009 Jan; 60(1):242-50. PubMed ID: 19116920 [TBL] [Abstract][Full Text] [Related]
5. Blau syndrome-associated mutations in exon 4 of the caspase activating recruitment domain 15 (CARD 15) gene are not found in ethnic Danes with sarcoidosis. Milman N; Nielsen FC; Hviid TV; Hansen Tv Clin Respir J; 2007 Dec; 1(2):74-9. PubMed ID: 20298285 [TBL] [Abstract][Full Text] [Related]
6. Analysis of a large kindred with Blau syndrome for HLA, autoimmunity, and sarcoidosis. Raphael SA; Blau EB; Zhang WH; Hsu SH Am J Dis Child; 1993 Aug; 147(8):842-8. PubMed ID: 8394645 [TBL] [Abstract][Full Text] [Related]
7. [Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations]. Kanazawa N Nihon Rinsho Meneki Gakkai Kaishi; 2007 Apr; 30(2):123-32. PubMed ID: 17473515 [TBL] [Abstract][Full Text] [Related]
8. [Blau syndrome or familial form of sarcoidosis with onset during infancy]. Moraillon I; Hayem F; Bourrillon A; Morel P; Rybojad M Ann Dermatol Venereol; 1996; 123(1):29-30. PubMed ID: 8734114 [TBL] [Abstract][Full Text] [Related]
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19. CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy. Wang X; Kuivaniemi H; Bonavita G; Mutkus L; Mau U; Blau E; Inohara N; Nunez G; Tromp G; Williams CJ Arthritis Rheum; 2002 Nov; 46(11):3041-5. PubMed ID: 12428248 [TBL] [Abstract][Full Text] [Related]
20. The influence of T cell receptor and cytokine genes on sarcoidosis susceptibility in African Americans. Rybicki BA; Maliarik MJ; Malvitz E; Sheffer RG; Major M; Popovich J; Iannuzzi MC Hum Immunol; 1999 Sep; 60(9):867-74. PubMed ID: 10527395 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]