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154 related items for PubMed ID: 15457465

  • 1. First report of systemic reactive (AA) amyloidosis in a patient with the hyperimmunoglobulinemia D with periodic fever syndrome.
    Obici L, Manno C, Muda AO, Picco P, D'Osualdo A, Palladini G, Avanzini MA, Torres D, Marciano S, Merlini G.
    Arthritis Rheum; 2004 Sep; 50(9):2966-9. PubMed ID: 15457465
    [Abstract] [Full Text] [Related]

  • 2. Hereditary periodic fever with systemic amyloidosis: is hyper-IgD syndrome really a benign disease?
    Siewert R, Ferber J, Horstmann RD, Specker C, Heering PJ, Timmann C.
    Am J Kidney Dis; 2006 Sep; 48(3):e41-5. PubMed ID: 16931207
    [Abstract] [Full Text] [Related]

  • 3. AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases.
    Lachmann HJ, Goodman HJ, Andrews PA, Gallagher H, Marsh J, Breuer S, Rowczenio DM, Bybee A, Hawkins PN.
    Arthritis Rheum; 2006 Jun; 54(6):2010-4. PubMed ID: 16732551
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary periodic fever].
    Lamprecht P, Timmann C, Ahmadi-Simab K, Gross WL.
    Internist (Berl); 2004 Aug; 45(8):904-11. PubMed ID: 15243709
    [Abstract] [Full Text] [Related]

  • 5. Periodic fever in children with hyperimmunoglobulinemia D and mevalonate kinase mutations.
    Grose C.
    Pediatr Infect Dis J; 2005 Jun; 24(6):573-4. PubMed ID: 15933578
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7. Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-igd and periodic fever syndrome: its application as a diagnostic tool.
    Simon A, Cuisset L, Vincent MF, van Der Velde-Visser SD, Delpech M, van Der Meer JW, Drenth JP.
    Ann Intern Med; 2001 Sep 04; 135(5):338-43. PubMed ID: 11529697
    [Abstract] [Full Text] [Related]

  • 8. Hereditary periodic fever and reactive amyloidosis.
    van der Hilst JC, Simon A, Drenth JP.
    Clin Exp Med; 2005 Oct 04; 5(3):87-98. PubMed ID: 16284730
    [Abstract] [Full Text] [Related]

  • 9. Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndrome.
    Takada K, Aksentijevich I, Mahadevan V, Dean JA, Kelley RI, Kastner DL.
    Arthritis Rheum; 2003 Sep 04; 48(9):2645-51. PubMed ID: 13130485
    [Abstract] [Full Text] [Related]

  • 10. Autoinflammatory diseases: the hereditary periodic fever syndromes.
    Fietta P.
    Acta Biomed; 2004 Aug 04; 75(2):92-9. PubMed ID: 15481697
    [Abstract] [Full Text] [Related]

  • 11. MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever.
    D'Osualdo A, Picco P, Caroli F, Gattorno M, Giacchino R, Fortini P, Corona F, Tommasini A, Salvi G, Specchia F, Obici L, Meini A, Ricci A, Seri M, Ravazzolo R, Martini A, Ceccherini I.
    Eur J Hum Genet; 2005 Mar 04; 13(3):314-20. PubMed ID: 15536479
    [Abstract] [Full Text] [Related]

  • 12. [MVK gene abnormality and new approach to treatment of hyper IgD syndrome and periodic fever syndrome].
    Naruto T.
    Nihon Rinsho Meneki Gakkai Kaishi; 2007 Apr 04; 30(2):86-9. PubMed ID: 17473510
    [Abstract] [Full Text] [Related]

  • 13. Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins.
    Hospach T, Lohse P, Heilbronner H, Dannecker GE, Lohse P.
    Arthritis Rheum; 2005 Nov 04; 52(11):3606-10. PubMed ID: 16255052
    [Abstract] [Full Text] [Related]

  • 14. Amyloidosis in a child with hyperimmunoglobulinemia D syndrome.
    Yel S, Gunduz Z, Bastug F, Dusunsel R, Dursun I, Poyrazoglu H, Tulpar S, Deniz K, Demirkaya E.
    Iran J Kidney Dis; 2013 Jan 04; 7(1):70-2. PubMed ID: 23314147
    [Abstract] [Full Text] [Related]

  • 15. Molecular mechanisms of amyloidosis.
    van der Hilst JC, Simon A, Drenth JP.
    N Engl J Med; 2003 Nov 06; 349(19):1872-3; author reply 1872-3. PubMed ID: 14606469
    [No Abstract] [Full Text] [Related]

  • 16. Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D.
    Frenkel J, Houten SM, Waterham HR, Wanders RJ, Rijkers GT, Duran M, Kuijpers TW, van Luijk W, Poll-The BT, Kuis W.
    Rheumatology (Oxford); 2001 May 06; 40(5):579-84. PubMed ID: 11371670
    [Abstract] [Full Text] [Related]

  • 17. AA amyloidosis complicating the hereditary periodic fever syndromes.
    Lane T, Loeffler JM, Rowczenio DM, Gilbertson JA, Bybee A, Russell TL, Gillmore JD, Wechalekar AD, Hawkins PN, Lachmann HJ.
    Arthritis Rheum; 2013 Apr 06; 65(4):1116-21. PubMed ID: 23280696
    [Abstract] [Full Text] [Related]

  • 18. Hyperimmunoglobulinemia D syndrome in an Arab child.
    Hammoudeh M.
    Clin Rheumatol; 2005 Feb 06; 24(1):92-4. PubMed ID: 15674660
    [Abstract] [Full Text] [Related]

  • 19. Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) in a child with normal serum IgD, but increased serum IgA concentration.
    Saulsbury FT.
    J Pediatr; 2003 Jul 06; 143(1):127-9. PubMed ID: 12915839
    [Abstract] [Full Text] [Related]

  • 20. [Periodic fever: the first Portuguese case-report of hyper-IgD syndrome (HIDS)].
    Abreu TT.
    Acta Med Port; 2004 Jul 06; 17(5):391-4. PubMed ID: 16197847
    [Abstract] [Full Text] [Related]

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