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6. Blau syndrome-associated uveitis and the NOD2 gene. Pillai P; Sobrin L Semin Ophthalmol; 2013; 28(5-6):327-32. PubMed ID: 24010719 [TBL] [Abstract][Full Text] [Related]
7. Clinical and genetic aspects of Blau syndrome: a 25-year follow-up of one family and a literature review. Punzi L; Furlan A; Podswiadek M; Gava A; Valente M; De Marchi M; Peserico A Autoimmun Rev; 2009 Jan; 8(3):228-32. PubMed ID: 18718560 [TBL] [Abstract][Full Text] [Related]
9. [The present and the prospect of study on Blau syndrome/early-onset sarcoidosis]. Nakano M; Kambe N Nihon Rinsho; 2013 Apr; 71(4):737-41. PubMed ID: 23678609 [TBL] [Abstract][Full Text] [Related]
10. Blau arteritis resembling Takayasu disease with a novel NOD2 mutation. Khubchandani RP; Hasija R; Touitou I; Khemani C; Wouters CH; Rose CD J Rheumatol; 2012 Sep; 39(9):1888-92. PubMed ID: 22859352 [TBL] [Abstract][Full Text] [Related]
13. A sporadic case of granulomatous disease negative for NOD2 mutations and mimicking Blau syndrome. Oda F; Murakami M; Hanakawa Y; Tohyama M; Nakano N; Nishikomori R; Kambe N; Sayama K Clin Exp Dermatol; 2018 Jan; 43(1):57-58. PubMed ID: 29082556 [No Abstract] [Full Text] [Related]
14. Sporadic Blau syndrome with onset of widespread granulomatous dermatitis in the newborn period. Stoevesandt J; Morbach H; Martin TM; Zierhut M; Girschick H; Hamm H Pediatr Dermatol; 2010; 27(1):69-73. PubMed ID: 20199415 [TBL] [Abstract][Full Text] [Related]
15. NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort. Aróstegui JI; Arnal C; Merino R; Modesto C; Antonia Carballo M; Moreno P; García-Consuegra J; Naranjo A; Ramos E; de Paz P; Rius J; Plaza S; Yagüe J Arthritis Rheum; 2007 Nov; 56(11):3805-13. PubMed ID: 17968944 [TBL] [Abstract][Full Text] [Related]
16. [Mutations of NOD2 gene and clinical features in Chinese Blau syndrome patients]. Wang W; Wei M; Song H; Qiu Z Zhonghua Er Ke Za Zhi; 2014 Dec; 52(12):896-901. PubMed ID: 25619344 [TBL] [Abstract][Full Text] [Related]
17. Type 1 T-helper cell predominance in granulomas of Crohn's disease. Kakazu T; Hara J; Matsumoto T; Nakamura S; Oshitani N; Arakawa T; Kitano A; Nakatani K; Kinjo F; Kuroki T Am J Gastroenterol; 1999 Aug; 94(8):2149-55. PubMed ID: 10445542 [TBL] [Abstract][Full Text] [Related]
18. Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism. Mensa-Vilaro A; Cham WT; Tang SP; Lim SC; González-Roca E; Ruiz-Ortiz E; Ariffin R; Yagüe J; Aróstegui JI Arthritis Rheumatol; 2016 Apr; 68(4):1039-44. PubMed ID: 26606664 [TBL] [Abstract][Full Text] [Related]
19. Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes. Rosé CD; Pans S; Casteels I; Anton J; Bader-Meunier B; Brissaud P; Cimaz R; Espada G; Fernandez-Martin J; Hachulla E; Harjacek M; Khubchandani R; Mackensen F; Merino R; Naranjo A; Oliveira-Knupp S; Pajot C; Russo R; Thomée C; Vastert S; Wulffraat N; Arostegui JI; Foley KP; Bertin J; Wouters CH Rheumatology (Oxford); 2015 Jun; 54(6):1008-16. PubMed ID: 25416713 [TBL] [Abstract][Full Text] [Related]
20. Blau syndrome, clinical and genetic aspects. Sfriso P; Caso F; Tognon S; Galozzi P; Gava A; Punzi L Autoimmun Rev; 2012 Nov; 12(1):44-51. PubMed ID: 22884558 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]