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.
142 related articles for article (PubMed ID: 15492850)
1. Novel mutations in TNFRSF1A in patients with typical tumor necrosis factor receptor-associated periodic syndrome and with systemic lupus erythematosus in Japanese. Horiuchi T; Tsukamoto H; Mitoma H; Miyagawa H; Tamimoto Y; Yoshizawa S; Harada M; Hayashi K; Hashimura C; Oribe M; Okamura S Int J Mol Med; 2004 Nov; 14(5):813-8. PubMed ID: 15492850 [TBL] [Abstract][Full Text] [Related]
2. A novel mutation (T61I) in the gene encoding tumour necrosis factor receptor superfamily 1A (TNFRSF1A) in a Japanese patient with tumour necrosis factor receptor-associated periodic syndrome (TRAPS) associated with systemic lupus erythematosus. Ida H; Kawasaki E; Miyashita T; Tanaka F; Kamachi M; Izumi Y; Huang M; Tamai M; Origuchi T; Kawakami A; Migita K; Motomura M; Yoshimura T; Eguchi K Rheumatology (Oxford); 2004 Oct; 43(10):1292-9. PubMed ID: 15280569 [TBL] [Abstract][Full Text] [Related]
3. Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatment. Stojanov S; Dejaco C; Lohse P; Huss K; Duftner C; Belohradsky BH; Herold M; Schirmer M Ann Rheum Dis; 2008 Sep; 67(9):1292-8. PubMed ID: 18180277 [TBL] [Abstract][Full Text] [Related]
4. Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes. Aganna E; Hammond L; Hawkins PN; Aldea A; McKee SA; van Amstel HK; Mischung C; Kusuhara K; Saulsbury FT; Lachmann HJ; Bybee A; McDermott EM; La Regina M; Arostegui JI; Campistol JM; Worthington S; High KP; Molloy MG; Baker N; Bidwell JL; Castañer JL; Whiteford ML; Janssens-Korpola PL; Manna R; Powell RJ; Woo P; Solis P; Minden K; Frenkel J; Yagüe J; Mirakian RM; Hitman GA; McDermott MF Arthritis Rheum; 2003 Sep; 48(9):2632-44. PubMed ID: 13130484 [TBL] [Abstract][Full Text] [Related]
5. Mannose binding lectin (MBL) gene mutation is not a risk factor for systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) in Japanese. Horiuchi T; Tsukamoto H; Morita C; Sawabe T; Harashima S; Nakashima H; Miyahara H; Hashimura C; Kondo M Genes Immun; 2000 Oct; 1(7):464-6. PubMed ID: 11196679 [TBL] [Abstract][Full Text] [Related]
6. An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome. Aganna E; Zeharia A; Hitman GA; Basel-Vanagaite L; Allotey RA; Booth DR; Hawkins PN; Thacker C; Syndercombe-Court D; McDermott MF Arthritis Rheum; 2002 Jan; 46(1):245-9. PubMed ID: 11817598 [TBL] [Abstract][Full Text] [Related]
7. Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa. Stojanov S; Lohse P; Lohse P; Hoffmann F; Renner ED; Zellerer S; Kéry A; Shin YS; Haas D; Hoffmann GF; Belohradsky BH Arthritis Rheum; 2004 Jun; 50(6):1951-8. PubMed ID: 15188372 [TBL] [Abstract][Full Text] [Related]
11. Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetrance. Aganna E; Aksentijevich I; Hitman GA; Kastner DL; Hoepelman AI; Posma FD; Zweers EJ; McDermott MF Eur J Hum Genet; 2001 Jan; 9(1):63-6. PubMed ID: 11175303 [TBL] [Abstract][Full Text] [Related]
12. The enlarging clinical, genetic, and population spectrum of tumor necrosis factor receptor-associated periodic syndrome. Dodé C; André M; Bienvenu T; Hausfater P; Pêcheux C; Bienvenu J; Lecron JC; Reinert P; Cattan D; Piette JC; Szajnert MF; Delpech M; Grateau G; Arthritis Rheum; 2002 Aug; 46(8):2181-8. PubMed ID: 12209523 [TBL] [Abstract][Full Text] [Related]
13. Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases. Kümpfel T; Hoffmann LA; Pellkofer H; Pöllmann W; Feneberg W; Hohlfeld R; Lohse P Neurology; 2008 Nov; 71(22):1812-20. PubMed ID: 19029521 [TBL] [Abstract][Full Text] [Related]
14. No association of polymorphisms in the tumor necrosis factor receptor I and receptor II genes with disease severity in rheumatoid arthritis. Glossop JR; Nixon NB; Dawes PT; Hassell AB; Mattey DL J Rheumatol; 2003 Jul; 30(7):1406-9. PubMed ID: 12858434 [TBL] [Abstract][Full Text] [Related]
15. Mutant tumor necrosis factor receptor associated with tumor necrosis factor receptor-associated periodic syndrome is altered antigenically and is retained within patients' leukocytes. Todd I; Radford PM; Daffa N; Bainbridge SE; Powell RJ; Tighe PJ Arthritis Rheum; 2007 Aug; 56(8):2765-73. PubMed ID: 17665435 [TBL] [Abstract][Full Text] [Related]
16. "Periodic fever" without fever: two cases of non-febrile TRAPS with mutations in the TNFRSF1A gene presenting with episodes of inflammation or monosymptomatic amyloidosis. Kallinich T; Haffner D; Rudolph B; Schindler R; Canaan-Kühl S; Keitzer R; Burmester GR; Roesen-Wolff A; Roesler J Ann Rheum Dis; 2006 Jul; 65(7):958-60. PubMed ID: 16308343 [TBL] [Abstract][Full Text] [Related]
17. A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family. Dodé C; Papo T; Fieschi C; Pêcheux C; Dion E; Picard F; Godeau P; Bienvenu J; Piette JC; Delpech M; Grateau G Arthritis Rheum; 2000 Jul; 43(7):1535-42. PubMed ID: 10902757 [TBL] [Abstract][Full Text] [Related]
18. A new mutation causing autosomal dominant periodic fever syndrome in a Danish family. Weyhreter H; Schwartz M; Kristensen TD; Valerius NH; Paerregaard A J Pediatr; 2003 Feb; 142(2):191-3. PubMed ID: 12584543 [TBL] [Abstract][Full Text] [Related]
19. Periodic fever (TRAPS) caused by mutations in the TNFalpha receptor 1 (TNFRSF1A) gene of three German patients. Rösen-Wolff A; Kreth HW; Hofmann S; Höhne K; Heubner G; Möbius D; Zintl F; Gahr M; Roesler J Eur J Haematol; 2001 Aug; 67(2):105-9. PubMed ID: 11722598 [TBL] [Abstract][Full Text] [Related]