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Journal Abstract Search

258 related items for PubMed ID: 11590390

  • 1. Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic fever.
    Hoffman HM, Wanderer AA, Broide DH.
    J Allergy Clin Immunol; 2001 Oct; 108(4):615-20. PubMed ID: 11590390
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  • 2. Identification of a locus on chromosome 1q44 for familial cold urticaria.
    Hoffman HM, Wright FA, Broide DH, Wanderer AA, Kolodner RD.
    Am J Hum Genet; 2000 May; 66(5):1693-8. PubMed ID: 10741953
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  • 5. Prevention of cold-associated acute inflammation in familial cold autoinflammatory syndrome by interleukin-1 receptor antagonist.
    Hoffman HM, Rosengren S, Boyle DL, Cho JY, Nayar J, Mueller JL, Anderson JP, Wanderer AA, Firestein GS.
    Lancet; 2000 May; 364(9447):1779-85. PubMed ID: 15541451
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  • 9. Familial cold auto-inflammatory syndrome (FCAS): characterization of symptomatology and impact on patients' lives.
    Stych B, Dobrovolny D.
    Curr Med Res Opin; 2008 Jun; 24(6):1577-82. PubMed ID: 18423104
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  • 10. Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.
    Aganna E, Martinon F, Hawkins PN, Ross JB, Swan DC, Booth DR, Lachmann HJ, Bybee A, Gaudet R, Woo P, Feighery C, Cotter FE, Thome M, Hitman GA, Tschopp J, McDermott MF.
    Arthritis Rheum; 2002 Sep; 46(9):2445-52. PubMed ID: 12355493
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  • 11. A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian origin.
    Shalev SA, Sprecher E, Indelman M, Hujirat Y, Bergman R, Rottem M.
    Int Arch Allergy Immunol; 2007 Sep; 143(3):190-3. PubMed ID: 17284928
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  • 12. New CIAS1 mutation and anakinra efficacy in overlapping of Muckle-Wells and familial cold autoinflammatory syndromes.
    Maksimovic L, Stirnemann J, Caux F, Ravet N, Rouaghe S, Cuisset L, Letellier E, Grateau G, Morin AS, Fain O.
    Rheumatology (Oxford); 2008 Mar; 47(3):309-10. PubMed ID: 18174231
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  • 15. New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.
    Dodé C, Le Dû N, Cuisset L, Letourneur F, Berthelot JM, Vaudour G, Meyrier A, Watts RA, Scott DG, Nicholls A, Granel B, Frances C, Garcier F, Edery P, Boulinguez S, Domergues JP, Delpech M, Grateau G.
    Am J Hum Genet; 2002 Jun; 70(6):1498-506. PubMed ID: 11992256
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  • 18. A pilot study to evaluate the safety and efficacy of the long-acting interleukin-1 inhibitor rilonacept (interleukin-1 Trap) in patients with familial cold autoinflammatory syndrome.
    Goldbach-Mansky R, Shroff SD, Wilson M, Snyder C, Plehn S, Barham B, Pham TH, Pucino F, Wesley RA, Papadopoulos JH, Weinstein SP, Mellis SJ, Kastner DL.
    Arthritis Rheum; 2008 Aug; 58(8):2432-42. PubMed ID: 18668591
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