• 1
    Delpech M, Grateau G. Genetically determined recurrent fevers. Curr Opin Immunol 2001; 13: 3942.
  • 2
    Sohar E, Gafni J, Pras M, Heller H. Familial Mediterranean fever: a survey of 470 cases and review of the literature. Am J Med 1967; 43: 22753.
  • 3
    Drenth JP, Haagsma CJ, van der Meer JW. Hyperimmunoglobulinemia D and periodic fever syndrome, the clinical spectrum in a series of 50 patients: International Hyper-IgD Study Group. Medicine (Baltimore) 1994; 73: 13344.
  • 4
    Bouroncle BA, Doan CA. Periodic fever: occurrence in five generations. Am J Med 1957; 23: 5026.
  • 5
    McDermott EM, Smillie DM, Powell RJ. Clinical spectrum of familial Hibernian fever: a 14-year follow-up study of the index case and extended family. Mayo Clin Proc 1997; 72: 80617.
  • 6
    Muckle TJ, Wells M. Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome. Q J Med 1962; 31: 23548.
  • 7
    A candidate gene for familial Mediterranean fever: French FMF Consortium. Nat Genet 1997; 17: 2531.
  • 8
    Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever: International FMF Consortium. Cell 1997; 90: 797807.
  • 9
    Drenth JP, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser SD, de Jong JG, et al. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. Nat Genet 1999; 22: 1803.
  • 10
    Houten SM, Kuis W, Duran M, de Koning TJ, van Royen-Kerkhof A, Romeijn GJ, et al. Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome. Nat Genet 1999; 22: 1757.
  • 11
    McDermott MF, Aksentijevich I, Galon J, McDermott E, Ogunkolade BW, Centola M, et al. Germline mutations in the extracellular domains of the 55kDa TNF receptor, TNFRSF1A, define a family of dominantly inherited autoinflammatory syndromes. Cell 1999; 97: 13344.
  • 12
    Cuisset L, Drenth JP, Berthelot JM, Meyrier A, Vaudour G, Watts RA, et al. Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44. Am J Hum Genet 1999; 65: 10549.
  • 13
    Hoffman HM, Mueller JL, Broide DH, Wanderer AA, Kolodner RD. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nat Genet 2001; 29: 3015.
  • 14
    Dodé C, Papo T, Fieschi C, Pêcheux C, Dion E, Picard F, et al. 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. Arthritis Rheum 2000; 43: 153542.
  • 15
    Simon A, Dodé C, van der Meer JW, Drenth JP. Familial periodic fever and amyloidosis due to a new mutation in the TNFRSF1A gene. Am J Med 2001; 110: 3136.
  • 16
    Jadoul M, Dode C, Cosyns JP, Abramowicz D, Georges B, Delpech M, et al. Autosomal-dominant periodic fever with AA amyloidosis: novel mutation in tumor necrosis factor receptor 1 gene. Kidney Int 2001; 59: 167782.
  • 17
    Aganna E, Aksentijevich I, Hitman GA, Kastner DL, Hoepelman AI, Posma FD, et al. Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetrance. Eur J Hum Genet 2001; 9: 636.
  • 18
    Aksentijevich I, Galon J, Soares M, Mansfield E, Hull K, Oh HH, et al. The tumor-necrosis-factor receptor-associated periodic syndrome: new mutations in TNFRSF1A, ancestral origins, genotype-phenotype studies, and evidence for further genetic heterogeneity of periodic fevers. Am J Hum Genet 2001; 69: 30114.
  • 19
    Simon A, van Deuren M, Tighe PJ, van der Meer JWM, Drenth JPH. Genetic analysis as a valuable key to diagnosis and treatment of periodic fever. Arch Intern Med 2001; 161: 24913.
  • 20
    Aganna E, Zeharia A, Hitman GA, Basel-Vanagaite L, Allotey RA, Booth DR, et al. An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor–associated periodic syndrome. Arthritis Rheum 2002; 46: 2459.
  • 21
    Sambrook J, Fritsch E, Maniatis TM. Molecular cloning: a laboratory manual. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press, 1989.
  • 22
    Underhill PA, Jin L, Lin AA, Mehdi SQ, Jenkins T, Vollrath D, et al. Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography. Genome Res 1997; 7: 9961005.
  • 23
    Jones AC, Austin J, Hansen N, Hoogendoorn B, Oefner PJ, Cheadle JP, et al. Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis. Clin Chem 1999; 45: 113340.
  • 24
    Levan-Petit I, Cardonna J, Garcia M, Migeon J, Corbi C, Preud'homme JL, et al. Sensitive ELISA for human immunoglobulin D measurement in neonate, infant, and adult sera. Clin Chem 2000; 46: 8768.
  • 25
    Toro JR, Aksentijevich I, Hull K, Dean J, Kastner DL. Tumor necrosis factor receptor-associated periodic syndrome: a novel syndrome with cutaneous manifestations. Arch Dermatol 2000; 136: 148794.
  • 26
    Adler Y, Finkelstein Y, Guindo J, Rodriguez de la Serna A, Shoenfeld Y, Bayes-Genis A, et al. Colchicine treatment for recurrent pericarditis: a decade of experience. Circulation 1998; 97: 21835.
  • 27
    Kees S, Langevitz P, Zemer D, Padeh S, Pras M, Livneh A. Attacks of pericarditis as a manifestation of familial Mediterranean fever (FMF). QJM 1997: 90: 6437.
  • 28
    Van der Meer JW, Vossen JM, Radl J, van Nieuwkoop JA, Meyer CJ, Lobatto S, et al. Hyperimmunoglobulinaemia D and periodic fever: a new syndrome. Lancet 1984; 1: 108790.
  • 29
    Livneh A, Drenth JP, Klasen IS, Langevitz P, George J, Shelton DA, et al. Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features. J Rheumatol 1997; 24: 155863.
  • 30
    Cazeneuve C, Ajrapetyan H, Papin S, Roudot-Thoraval F, Geneviève D, Mndjoyan E, et al. Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever. Am J Hum Genet 2000; 67: 113643.
  • 31
    Moriguchi M, Terai C, Kaneko H, Koseki Y, Kajiyama H, Uesato M, et al. A novel single-nucleotide polymorphism at the 5′-flanking region of SAA1 associated with risk of type AA amyloidosis secondary to rheumatoid arthritis. Arthritis Rheum 2001; 44: 126672.
  • 32
    Cattan D, Notarnicola C, Molinari N, Touitou I. Inflammatory bowel disease in non-Ashkenazi Jews with familial Mediterranean fever. Lancet 2000; 355: 3789.
  • 33
    Targan SR, Hanauer SB, van Deventer SJ, Mayer L, Present DH, Braakman T, et al. A short-term study of chimeric monoclonal antibody cA2 to tumor necrosis factor alpha for Crohn's disease: Crohn's Disease cA2 Study Group. N Engl J Med 1997; 37: 102935.
  • 34
    André M, Aumaître O, Papo T, Kemeny J-L, Vital-Durand D, Rousset H, et al. Disseminated aseptic abscesses associated with Crohn's disease: a new entity? Dig Dis Sci 1998; 43: 4208.