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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

231 related items for PubMed ID: 16931207

  • 1. 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]

  • 2. Hyperimmunoglobulinemia D and periodic fever syndrome. The clinical spectrum in a series of 50 patients. International Hyper-IgD Study Group.
    Drenth JP, Haagsma CJ, van der Meer JW.
    Medicine (Baltimore); 1994 May; 73(3):133-44. PubMed ID: 8190036
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Crescentic glomerulonephritis in hyper IgD syndrome.
    Tsimaratos M, Koné-Paut I, Daniel L, Gubler MC, Dussol B, Picon G.
    Pediatr Nephrol; 1999 Feb; 13(2):132-4. PubMed ID: 10229000
    [Abstract] [Full Text] [Related]

  • 5. [Periodic fever: the first Portuguese case-report of hyper-IgD syndrome (HIDS)].
    Abreu TT.
    Acta Med Port; 2004 Feb; 17(5):391-4. PubMed ID: 16197847
    [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. [Hyper-IgD syndrome (HIDS)].
    Scolozzi R.
    Recenti Prog Med; 1995 Jun; 86(6):243-7. PubMed ID: 7624586
    [Abstract] [Full Text] [Related]

  • 8. 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; 13(3):314-20. PubMed ID: 15536479
    [Abstract] [Full Text] [Related]

  • 9. Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features.
    Livneh A, Drenth JP, Klasen IS, Langevitz P, George J, Shelton DA, Gumucio DL, Pras E, Kastner DL, Pras M, van der Meer JW.
    J Rheumatol; 1997 Aug; 24(8):1558-63. PubMed ID: 9263151
    [Abstract] [Full Text] [Related]

  • 10. [Hyperimmunoglobulinemia D--a new periodic syndrome with features simulating familial Mediterranean fever].
    Livneh A, Langevitz P.
    Harefuah; 1996 Oct; 131(7-8):283-4. PubMed ID: 8940530
    [No Abstract] [Full Text] [Related]

  • 11. 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; 143(1):127-9. PubMed ID: 12915839
    [Abstract] [Full Text] [Related]

  • 12. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.
    Drenth JP, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser SD, de Jong JG, Beckmann JS, van der Meer JW, Delpech M.
    Nat Genet; 1999 Jun; 22(2):178-81. PubMed ID: 10369262
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [Hyperimmunoglobulinemia D or periodic fever syndrome. Cutaneous manifestations in 3 cases].
    Cartier H, Guillet MH, Lemoigne E, Sassolas B, Leroy JP, Mottier D, Guillet G.
    Ann Dermatol Venereol; 1996 Jun; 123(5):314-21. PubMed ID: 8761083
    [Abstract] [Full Text] [Related]

  • 15. Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome.
    van der Hilst JC, Drenth JP, Bodar EJ, Bijzet J, van der Meer JW, Simon A, International HIDS Study Group.
    Amyloid; 2005 Jun; 12(2):115-9. PubMed ID: 16011988
    [Abstract] [Full Text] [Related]

  • 16. IgD immune complex vasculitis in a patient with hyperimmunoglobulinemia D and periodic fever.
    Boom BW, Daha MR, Vermeer BJ, van der Meer JW.
    Arch Dermatol; 1990 Dec; 126(12):1621-4. PubMed ID: 2147822
    [Abstract] [Full Text] [Related]

  • 17. Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever.
    Schlabe S, Schwarze-Zander C, Lohse P, Rockstroh JK.
    BMJ Case Rep; 2016 Nov 29; 2016():. PubMed ID: 27899390
    [Abstract] [Full Text] [Related]

  • 18. Overt and occult rheumatic diseases: the child with chronic fever.
    Frenkel J, Kuis W.
    Best Pract Res Clin Rheumatol; 2002 Jul 29; 16(3):443-69. PubMed ID: 12387810
    [Abstract] [Full Text] [Related]

  • 19. First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome.
    Rigante D, Capoluongo E, Bertoni B, Ansuini V, Chiaretti A, Piastra M, Pulitanò S, Genovese O, Compagnone A, Stabile A.
    Arthritis Rheum; 2007 Feb 29; 56(2):658-61. PubMed ID: 17265501
    [Abstract] [Full Text] [Related]

  • 20. 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 29; 52(11):3606-10. PubMed ID: 16255052
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.