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Journal Abstract Search

131 related items for PubMed ID: 11722598

  • 1. 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
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  • 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
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  • 6. 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
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  • 7. 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
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  • 8. 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
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  • 10. Shedding of mutant tumor necrosis factor receptor superfamily 1A associated with tumor necrosis factor receptor-associated periodic syndrome: differences between cell types.
    Huggins ML, Radford PM, McIntosh RS, Bainbridge SE, Dickinson P, Draper-Morgan KA, Tighe PJ, Powell RJ, Todd I.
    Arthritis Rheum; 2004 Aug; 50(8):2651-9. PubMed ID: 15334481
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  • 13. Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis.
    Kallinich T, Briese S, Roesler J, Rudolph B, Sarioglu N, Blankenstein O, Keitzer R, Querfeld U, Haffner D.
    J Rheumatol; 2004 Dec; 31(12):2519-22. PubMed ID: 15570662
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  • 14. Severe TNF receptor-associated periodic syndrome due to 2 TNFRSF1A mutations including a new F60V substitution.
    Haas SL, Lohse P, Schmitt WH, Hildenbrand R, Karaorman M, Singer MV, Böcker U.
    Gastroenterology; 2006 Jan; 130(1):172-8. PubMed ID: 16401480
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  • 16. Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) or familial Hibernian fever: presentation in a four-day-old infant.
    Savage T, Loftus BG, Tormey V, McDermott MF, Moylett E.
    J Clin Rheumatol; 2008 Dec; 14(6):342-5. PubMed ID: 18690165
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  • 17. Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics.
    Lainka E, Neudorf U, Lohse P, Timmann C, Stojanov S, Huss K, von Kries R, Niehues T.
    Rheumatology (Oxford); 2009 Aug; 48(8):987-91. PubMed ID: 19541728
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  • 18. Autosomal dominant periodic fever with AA amyloidosis: tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Turkish family.
    Dinc A, Erdem H, Rowczenio D, Simsek I, Pay S, Bahce M, Lachmann H.
    J Nephrol; 2005 Aug; 18(5):626-9. PubMed ID: 16299693
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  • 20. 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 25; 71(22):1812-20. PubMed ID: 19029521
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