These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients--expanding phenotype of CIAS1 related autoinflammatory syndrome. Pörksen G; Lohse P; Rösen-Wolff A; Heyden S; Förster T; Wendisch J; Heubner G; Bernuth H; Sallmann S; Gahr M; Roesler J Eur J Haematol; 2004 Aug; 73(2):123-7. PubMed ID: 15245511 [TBL] [Abstract][Full Text] [Related]
24. Positive clinical and biochemical responses to anakinra in a 3-yr-old patient with cryopyrin-associated periodic syndrome (CAPS). Ramos E; Aróstegui JI; Campuzano S; Rius J; Bousoño C; Yagüe J Rheumatology (Oxford); 2005 Aug; 44(8):1072-3. PubMed ID: 15840596 [No Abstract] [Full Text] [Related]
25. A cryopyrin-associated periodic syndrome with joint destruction. Lequerré T; Vittecoq O; Saugier-Veber P; Goldenberg A; Patoz P; Frébourg T; Le Loët X Rheumatology (Oxford); 2007 Apr; 46(4):709-14. PubMed ID: 17178739 [TBL] [Abstract][Full Text] [Related]
26. Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P. Hoffman HM; Gregory SG; Mueller JL; Tresierras M; Broide DH; Wanderer AA; Kolodner RD Hum Genet; 2003 Feb; 112(2):209-16. PubMed ID: 12522564 [TBL] [Abstract][Full Text] [Related]
27. Muckle-Wells syndrome without mutation in exon 3 of the NLRP3 gene, identified by evidence of excessive monocyte production of functional interleukin 1β and rapid response to anakinra. Sabroe RA; Stokes CA; Parker LC; Higgins K; Prince LR; Sabroe I Clin Exp Dermatol; 2013 Dec; 38(8):874-7. PubMed ID: 23889084 [TBL] [Abstract][Full Text] [Related]
28. Gene polymorphisms in the NALP3 inflammasome are associated with interleukin-1 production and severe inflammation: relation to common inflammatory diseases? Verma D; Lerm M; Blomgran Julinder R; Eriksson P; Söderkvist P; Särndahl E Arthritis Rheum; 2008 Mar; 58(3):888-94. PubMed ID: 18311798 [TBL] [Abstract][Full Text] [Related]
29. [Clinical features of CINCA syndrome: effects and problems of IL-1Ra]. Sugiura H; Matsubayashi T Nihon Rinsho Meneki Gakkai Kaishi; 2007 Apr; 30(2):108-13. PubMed ID: 17473513 [TBL] [Abstract][Full Text] [Related]
30. Anakinra in mutation-negative NOMID/CINCA syndrome: comment on the articles by Hawkins et al and Hoffman and Patel. Frenkel J; Wulffraat NM; Kuis W Arthritis Rheum; 2004 Nov; 50(11):3738-9; author reply 3739-40. PubMed ID: 15529342 [No Abstract] [Full Text] [Related]
31. [Fever from the cold--familial cold autoinflammatory syndrome]. Alhopuro P; Klimenko T; Aittomäki K Duodecim; 2009; 125(5):542-5. PubMed ID: 19385344 [TBL] [Abstract][Full Text] [Related]
32. A fever gene comes in from the cold. Kastner DL; O'Shea JJ Nat Genet; 2001 Nov; 29(3):241-2. PubMed ID: 11687785 [No Abstract] [Full Text] [Related]
33. Cryopyrin-associated autoinflammatory syndrome: a new mutation. Zeft A; Bohnsack JF Ann Rheum Dis; 2007 Jun; 66(6):843-4. PubMed ID: 17513575 [No Abstract] [Full Text] [Related]
34. Autoinflammatory gene mutations in Behçet's disease. Koné-Paut I; Sanchez E; Le Quellec A; Manna R; Touitou I Ann Rheum Dis; 2007 Jun; 66(6):832-4. PubMed ID: 17213252 [TBL] [Abstract][Full Text] [Related]
35. The T348M mutated form of cryopyrin is associated with defective lipopolysaccharide-induced interleukin 10 production in CINCA syndrome. Bihl T; Vassina E; Boettger MK; Goldbach-Mansky R; Seitz M; Villiger PM; Simon HU Ann Rheum Dis; 2005 Sep; 64(9):1380-1. PubMed ID: 16100350 [No Abstract] [Full Text] [Related]
36. A novel CIAS1 mutation and plasma/cerebrospinal fluid cytokine profile in a German patient with neonatal-onset multisystem inflammatory disease responsive to methotrexate therapy. Stojanov S; Weiss M; Lohse P; Belohradsky BH Pediatrics; 2004 Jul; 114(1):e124-7. PubMed ID: 15231984 [TBL] [Abstract][Full Text] [Related]
37. Somatic mosaicism of CIAS1 in a patient with chronic infantile neurologic, cutaneous, articular syndrome. Saito M; Fujisawa A; Nishikomori R; Kambe N; Nakata-Hizume M; Yoshimoto M; Ohmori K; Okafuji I; Yoshioka T; Kusunoki T; Miyachi Y; Heike T; Nakahata T Arthritis Rheum; 2005 Nov; 52(11):3579-85. PubMed ID: 16255047 [TBL] [Abstract][Full Text] [Related]
38. Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome. Hentgen V; Despert V; Leprêtre AC; Cuisset L; Chevrant-Breton J; Jégo P; Chalès G; Gall EL; Delpech M; Grateau G J Rheumatol; 2005 Apr; 32(4):747-51. PubMed ID: 15801036 [TBL] [Abstract][Full Text] [Related]
39. New insights into the nature of autoinflammatory diseases from mice with Nlrp3 mutations. Meng G; Strober W Eur J Immunol; 2010 Mar; 40(3):649-53. PubMed ID: 20201022 [TBL] [Abstract][Full Text] [Related]
40. Controlling inflammation: contemporary treatments for autoinflammatory diseases and syndromes. Sterba G; Sterba Y Dermatol Clin; 2013 Jul; 31(3):507-11. PubMed ID: 23827252 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]