메뉴 건너뛰기




Volumn 75, Issue 2, 2004, Pages

Autoinflammatory diseases: The hereditary periodic fever syndromes

Author keywords

Familial Mediterranean fever; Hereditary periodic fever syndromes; Human autoinflammatory diseases; Hyperimmunoglobulinemia D and periodic fever syndrome; Tumor necrosis factor receptor superfamily 1A associated periodic syndrome

Indexed keywords

COLCHICINE; CORTICOSTEROID; ETANERCEPT; GENE PRODUCT; MARENOSTRIN; MEVALONATE KINASE; MEVALONIC ACID; PROTEIN KINASE; TUMOR NECROSIS FACTOR RECEPTOR 1; UNCLASSIFIED DRUG;

EID: 19444373105     PISSN: 03924203     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (30)

References (55)
  • 2
    • 0037216780 scopus 로고    scopus 로고
    • The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations
    • Hull KM, Shoham N, Chae JJ, Aksentijevich I, Kastner DL. The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations. Curr Opin Rheumatol 2003; 15: 61-9.
    • (2003) Curr Opin Rheumatol , vol.15 , pp. 61-69
    • Hull, K.M.1    Shoham, N.2    Chae, J.J.3    Aksentijevich, I.4    Kastner, D.L.5
  • 4
    • 0035479996 scopus 로고    scopus 로고
    • Genetically determined recurrent fevers
    • Delpech M, Grateau G. Genetically determined recurrent fevers. Curr Opin Immunol 2001; 13: 539-42.
    • (2001) Curr Opin Immunol , vol.13 , pp. 539-542
    • Delpech, M.1    Grateau, G.2
  • 5
    • 0036657283 scopus 로고    scopus 로고
    • Fire and ICE: The role of pyrin domain-containing proteins in inflammation and apoptosis
    • Gumucio DL, Diaz A, Schaner P, et al. Fire and ICE: the role of pyrin domain-containing proteins in inflammation and apoptosis. Clin Exp Rheumatol 2002; 20 (Suppl. 26): S45-S53.
    • (2002) Clin Exp Rheumatol , vol.20 , Issue.SUPPL. 26
    • Gumucio, D.L.1    Diaz, A.2    Schaner, P.3
  • 6
    • 0036733312 scopus 로고    scopus 로고
    • The TNF receptor-associated periodic syndrome (TRAPS). Emerging concepts of an autoinflammatory disorder
    • Hull KM, Drewe E, Aksentijevich I, et al. The TNF receptor-associated periodic syndrome (TRAPS). Emerging concepts of an autoinflammatory disorder. Medicine (Baltimore) 2002; 81: 349-68.
    • (2002) Medicine (Baltimore) , vol.81 , pp. 349-368
    • Hull, K.M.1    Drewe, E.2    Aksentijevich, I.3
  • 7
    • 0035719198 scopus 로고    scopus 로고
    • Familial Mediterranean fever. A review and update
    • Orbach H, Ben-Chetrit E. Familial Mediterranean fever. A review and update. Minerva Med 2001; 92: 421-30.
    • (2001) Minerva Med , vol.92 , pp. 421-430
    • Orbach, H.1    Ben-Chetrit, E.2
  • 8
    • 0028235339 scopus 로고
    • The clinical features of familial Mediterranean fever of elderly onset
    • Rozenbaum M, Rosner I. The clinical features of familial Mediterranean fever of elderly onset. Clin Exp Rheumatol 1994; 12: 347-8.
    • (1994) Clin Exp Rheumatol , vol.12 , pp. 347-348
    • Rozenbaum, M.1    Rosner, I.2
  • 9
    • 0030469361 scopus 로고    scopus 로고
    • The changing face of familial Mediterranean fever
    • Livneh A, Langevitz P, Zemer D, et al. The changing face of familial Mediterranean fever. Semin Arthritis Rheum 1996; 26: 612-27.
    • (1996) Semin Arthritis Rheum , vol.26 , pp. 612-627
    • Livneh, A.1    Langevitz, P.2    Zemer, D.3
  • 11
    • 0033768510 scopus 로고    scopus 로고
    • A survey of phenotype II in familial Mediterranean fever
    • Mehkoglu M, Ozdogan H, Korkmaz C, et al. A survey of phenotype II in familial Mediterranean fever. Ann Rheum Dis 2000; 59: 910-3.
    • (2000) Ann Rheum Dis , vol.59 , pp. 910-913
    • Mehkoglu, M.1    Ozdogan, H.2    Korkmaz, C.3
  • 12
    • 0026653798 scopus 로고
    • Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16
    • Pras E, Aksentijevich I, Gruberg L, Balow JE Jr, Prosen L, Dean M. Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16. N Engl J Med 1992; 326: 1509-13.
    • (1992) N Engl J Med , vol.326 , pp. 1509-1513
    • Pras, E.1    Aksentijevich, I.2    Gruberg, L.3    Balow Jr., J.E.4    Prosen, L.5    Dean, M.6
  • 13
    • 0343674694 scopus 로고    scopus 로고
    • Mutations in the MEFVgene in a large series of patients with a clinical diagnosis of familial Mediterranean fever
    • Dodé C, Pécheux C, Cazeneuve C, et al. Mutations in the MEFVgene in a large series of patients with a clinical diagnosis of familial Mediterranean fever. Am J Med Genet 2000; 92: 241-6.
    • (2000) Am J Med Genet , vol.92 , pp. 241-246
    • Dodé, C.1    Pécheux, C.2    Cazeneuve, C.3
  • 14
    • 0036224497 scopus 로고    scopus 로고
    • The different contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever
    • Gershoni-Baruch R, Brik R, Shinavi M, Livneh A. The different contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever. Eur J Hum Genet 2002; 10: 145-9.
    • (2002) Eur J Hum Genet , vol.10 , pp. 145-149
    • Gershoni-Baruch, R.1    Brik, R.2    Shinavi, M.3    Livneh, A.4
  • 15
    • 0038141040 scopus 로고    scopus 로고
    • Familial Mediterranean fever (FMF) and renal AA amyloidosis. Phenotype-genotype correlation, treatment and prognosis
    • Ben-Chetrit E. Familial Mediterranean fever (FMF) and renal AA amyloidosis. Phenotype-genotype correlation, treatment and prognosis. J Nephrol 2003; 16: 431-4.
    • (2003) J Nephrol , vol.16 , pp. 431-434
    • Ben-Chetrit, E.1
  • 16
    • 0035882523 scopus 로고    scopus 로고
    • Common MEFV mutations among Jewish ethnic groups in Israel: High frequency of carrier and phenotype III states and absence of a perceptible biological advantage for the carrier state
    • Kogan A, Shinar Y, Lidar M, et al. Common MEFV mutations among Jewish ethnic groups in Israel: high frequency of carrier and phenotype III states and absence of a perceptible biological advantage for the carrier state. Am J Med Genet 2001; 102: 272-6.
    • (2001) Am J Med Genet , vol.102 , pp. 272-276
    • Kogan, A.1    Shinar, Y.2    Lidar, M.3
  • 17
    • 0034164577 scopus 로고    scopus 로고
    • The E148Q mutation in the MEFVgene: Is it a disease-causing mutation or a sequence variant?
    • Ben-Chetrit E, Lerer I, Malamud E, Domingo C, Abeliovich D. The E148Q mutation in the MEFVgene: is it a disease-causing mutation or a sequence variant? Hum Mutat 2000; 15: 385-6.
    • (2000) Hum Mutat , vol.15 , pp. 385-386
    • Ben-Chetrit, E.1    Lerer, I.2    Malamud, E.3    Domingo, C.4    Abeliovich, D.5
  • 18
    • 13144307083 scopus 로고    scopus 로고
    • Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever
    • Dewalle M, Domingo C, Rozenbaum M, et al. Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever. Eur J Hum Genet 1998; 6: 95-7.
    • (1998) Eur J Hum Genet , vol.6 , pp. 95-97
    • Dewalle, M.1    Domingo, C.2    Rozenbaum, M.3
  • 19
    • 0035147039 scopus 로고    scopus 로고
    • The MICA region determines the first modifier locus in familial Mediterranean fever
    • Touitou I, Picot MC, Domingo C, et al. The MICA region determines the first modifier locus in familial Mediterranean fever. Arthritis Rheum 2001; 44: 163-9.
    • (2001) Arthritis Rheum , vol.44 , pp. 163-169
    • Touitou, I.1    Picot, M.C.2    Domingo, C.3
  • 20
    • 0033754004 scopus 로고    scopus 로고
    • Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever
    • Cazeneuve C, Ajrapctyan H, Papin S, et al. Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever. Am J Hum Genet 2000; 67: 1136-43.
    • (2000) Am J Hum Genet , vol.67 , pp. 1136-1143
    • Cazeneuve, C.1    Ajrapctyan, H.2    Papin, S.3
  • 21
    • 0942287854 scopus 로고    scopus 로고
    • A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: An unusual familial Mediterranean fever phenotype or another MEFV-associated periodic inflammatory disorder?
    • Aldea A, Campistol JM, Arostegui JI, et al. A severe autosomal-dominant periodic inflammatory disorder with renal AA amyloidosis and colchicine resistance associated to the MEFV H478Y variant in a Spanish kindred: an unusual familial Mediterranean fever phenotype or another MEFV-associated periodic inflammatory disorder? Am J Med Genet 2004; 124A: 67-73.
    • (2004) Am J Med Genet , vol.124 A , pp. 67-73
    • Aldea, A.1    Campistol, J.M.2    Arostegui, J.I.3
  • 22
    • 0034658465 scopus 로고    scopus 로고
    • The gene for familial Mediterranean fever, MEFV, is expressed in early leukocyte development and is regulated in response to inflammatory mediators
    • Centola M, Wood G, Frucht DM, et al. The gene for familial Mediterranean fever, MEFV, is expressed in early leukocyte development and is regulated in response to inflammatory mediators. Blood 2000; 95: 3223-31.
    • (2000) Blood , vol.95 , pp. 3223-3231
    • Centola, M.1    Wood, G.2    Frucht, D.M.3
  • 23
    • 0344823965 scopus 로고    scopus 로고
    • Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathways
    • Shoham NG, Centola M, Mansfield E, et al. Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathways. Proc Natl Acad Sci USA 2003; 100: 13501-6.
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 13501-13506
    • Shoham, N.G.1    Centola, M.2    Mansfield, E.3
  • 25
    • 0036481524 scopus 로고    scopus 로고
    • Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean fever
    • Notarnicola C, Didelot MN, Seguret F, Demaille J, Touitou I. Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean fever. Genes Immun 2002; 3: 43-5.
    • (2002) Genes Immun , vol.3 , pp. 43-45
    • Notarnicola, C.1    Didelot, M.N.2    Seguret, F.3    Demaille, J.4    Touitou, I.5
  • 26
    • 0037308317 scopus 로고    scopus 로고
    • Increased soluble FAS suggests delayed apoptosis in familial Mediterranean fever complicated with amyloidosis
    • Kiraz S, Ertenli I, Ozturk MA, et al. Increased soluble FAS suggests delayed apoptosis in familial Mediterranean fever complicated with amyloidosis. J Rheumatol 2003; 30: 313-5.
    • (2003) J Rheumatol , vol.30 , pp. 313-315
    • Kiraz, S.1    Ertenli, I.2    Ozturk, M.A.3
  • 27
    • 0031693188 scopus 로고    scopus 로고
    • The hereditary periodic fever syndromes: Molecular analysis of a new family of inflammatory diseases
    • Centola M, Aksentijevich I, Kastner DL. The hereditary periodic fever syndromes: molecular analysis of a new family of inflammatory diseases. Hum Mol Genet 1998; 7: 1581-8.
    • (1998) Hum Mol Genet , vol.7 , pp. 1581-1588
    • Centola, M.1    Aksentijevich, I.2    Kastner, D.L.3
  • 28
    • 0030783102 scopus 로고    scopus 로고
    • Criteria for the diagnosis of familial Mediterranean fever
    • Livneh A, Langevitz P, Zemer D, et al. Criteria for the diagnosis of familial Mediterranean fever. Arthritis Rheum 1997; 40: 1879-85.
    • (1997) Arthritis Rheum , vol.40 , pp. 1879-1885
    • Livneh, A.1    Langevitz, P.2    Zemer, D.3
  • 30
    • 0032964187 scopus 로고    scopus 로고
    • Activation of the cytokine network in familial Mediterranean fever
    • Gang N, Drenth JP, Langevitz P, et al. Activation of the cytokine network in familial Mediterranean fever. J Rheumatol 1999; 26: 890-7.
    • (1999) J Rheumatol , vol.26 , pp. 890-897
    • Gang, N.1    Drenth, J.P.2    Langevitz, P.3
  • 31
  • 32
    • 0035666961 scopus 로고    scopus 로고
    • Familial Mediterranean fever: Association with elevated IgD plasma levels with specific MEFV mutations
    • Medlej-Hashim M, Petit I, Adib S, et al. Familial Mediterranean fever: association with elevated IgD plasma levels with specific MEFV mutations. Eur J Hum Genet 2001; 9: 849-54.
    • (2001) Eur J Hum Genet , vol.9 , pp. 849-854
    • Medlej-Hashim, M.1    Petit, I.2    Adib, S.3
  • 34
    • 0141669159 scopus 로고    scopus 로고
    • Familial Mediterranean fever in 2003. Pathogenesis and management
    • Tunca M, Ben-Chetrit E. Familial Mediterranean fever in 2003. Pathogenesis and management. Clin Exp Rheumatol 2003; 21 (Suppl. 30): S49-S52.
    • (2003) Clin Exp Rheumatol , vol.21 , Issue.SUPPL. 30
    • Tunca, M.1    Ben-Chetrit, E.2
  • 35
    • 0033861821 scopus 로고    scopus 로고
    • Mevalonate kinase deficiency and Dutch type periodic fever
    • Frenkel J, Houten SM, Waterham HR, et al. Mevalonate kinase deficiency and Dutch type periodic fever. Clin Exp Rheumatol 2000; 18: 525-32.
    • (2000) Clin Exp Rheumatol , vol.18 , pp. 525-532
    • Frenkel, J.1    Houten, S.M.2    Waterham, H.R.3
  • 36
    • 0030878782 scopus 로고    scopus 로고
    • Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: Two diseases with distinct clinical, serologic and genetic features
    • Livneh A, Drenth JP, Klasen IS, et al. Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic and genetic features. J Rheumatol 1997; 24: 1558-63.
    • (1997) J Rheumatol , vol.24 , pp. 1558-1563
    • Livneh, A.1    Drenth, J.P.2    Klasen, I.S.3
  • 38
    • 0033039501 scopus 로고    scopus 로고
    • 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, et al. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group. Nat Genet 1999; 22: 178-81.
    • (1999) Nat Genet , vol.22 , pp. 178-181
    • Drenth, J.P.1    Cuisset, L.2    Grateau, G.3
  • 39
    • 0036822810 scopus 로고    scopus 로고
    • Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome
    • Frenkel J, Rijkers GT, Mandey SH, et al. Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 2002; 46: 2794-803.
    • (2002) Arthritis Rheum , vol.46 , pp. 2794-2803
    • Frenkel, J.1    Rijkers, G.T.2    Mandey, S.H.3
  • 40
    • 0028979302 scopus 로고
    • Interferon-gamma and urine neopterin in attacks of hyperimmunoglobulinemia D and periodic fever syndrome
    • Drenth JP, Powell RJ, Brown NS, van der Meer JW. Interferon-gamma and urine neopterin in attacks of hyperimmunoglobulinemia D and periodic fever syndrome. Eur J Clin Invest 1995; 25: 683-6.
    • (1995) Eur J Clin Invest , vol.25 , pp. 683-686
    • Drenth, J.P.1    Powell, R.J.2    Brown, N.S.3    Van Der Meer, J.W.4
  • 41
    • 0035055571 scopus 로고    scopus 로고
    • Molecular analysis of MVK mutations and enzymatic activity in hyper IgD and periodic fever syndrome
    • Cuisset L, Drenth JP, Simon A, et al. Molecular analysis of MVK mutations and enzymatic activity in hyper IgD and periodic fever syndrome. Eur J Hum Genet 2001; 9: 260-6.
    • (2001) Eur J Hum Genet , vol.9 , pp. 260-266
    • Cuisset, L.1    Drenth, J.P.2    Simon, A.3
  • 42
    • 4644299105 scopus 로고    scopus 로고
    • Major mutation of the hyper-IgD and periodic fever syndrome originates from one common ancestor - Truly Dutch type periodic fever?
    • Simon A, Mariman EC, van der Meer JWM, Drenth JP. Major mutation of the hyper-IgD and periodic fever syndrome originates from one common ancestor - truly Dutch type periodic fever? Clin Exp Rheumatol 2002; 20 (Suppl. 26): S-74.
    • (2002) Clin Exp Rheumatol , vol.20 , Issue.SUPPL. 26
    • Simon, A.1    Mariman, E.C.2    Van Der Meer, J.W.M.3    Drenth, J.P.4
  • 43
    • 0027529504 scopus 로고
    • Clinical and biochemical phenotype in 11 patients with mevalonic aciduria
    • Hoffmann GF, Charpentier C, Mayatepek E, et al. Clinical and biochemical phenotype in 11 patients with mevalonic aciduria. Pediatrics 1993; 91: 915-21.
    • (1993) Pediatrics , vol.91 , pp. 915-921
    • Hoffmann, G.F.1    Charpentier, C.2    Mayatepek, E.3
  • 44
    • 0032987982 scopus 로고    scopus 로고
    • Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinemia D and periodic fever syndrome
    • Houten SM, Kuis W, Duran M, et al. Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinemia D and periodic fever syndrome. Nat Genet 1999; 22: 175-7.
    • (1999) Nat Genet , vol.22 , pp. 175-177
    • Houten, S.M.1    Kuis, W.2    Duran, M.3
  • 45
    • 0038724543 scopus 로고    scopus 로고
    • Isoprenoid biosynthesis in hereditary periodic fever syndromes and inflammation
    • Houten SM, Frenkel J, Waterham HR. Isoprenoid biosynthesis in hereditary periodic fever syndromes and inflammation. Cell Mol Life Sci 2003; 60: 1118-34.
    • (2003) Cell Mol Life Sci , vol.60 , pp. 1118-1134
    • Houten, S.M.1    Frenkel, J.2    Waterham, H.R.3
  • 46
    • 0034888835 scopus 로고    scopus 로고
    • Limited efficacy of thalidomide in the treatment of febrile attacks of the hyper-IgD and periodic fever syndrome: A randomized, double blind, placebo controlled trial
    • Drenth JP, Vonk AG, Simon A, Powell R, van der Meer JW. Limited efficacy of thalidomide in the treatment of febrile attacks of the hyper-IgD and periodic fever syndrome: a randomized, double blind, placebo controlled trial. J Pharmacol Exp Ther 2001; 298: 1221-6.
    • (2001) J Pharmacol Exp Ther , vol.298 , pp. 1221-1226
    • Drenth, J.P.1    Vonk, A.G.2    Simon, A.3    Powell, R.4    Van Der Meer, J.W.5
  • 47
    • 0141453408 scopus 로고    scopus 로고
    • 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. Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndrome. Arthritis Rheum 2003; 48: 2645-51.
    • (2003) Arthritis Rheum , vol.48 , pp. 2645-2651
    • Takada, K.1    Aksentijevich, I.2    Mahadevan, V.3    Dean, J.A.4    Kelley, R.I.5    Kastner, D.L.6
  • 49
    • 0033515520 scopus 로고    scopus 로고
    • Germline mutations in the extracellular domains of the 55kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
    • McDermott MF, Aksentijevich I, Galon J, et al. Germline mutations in the extracellular domains of the 55kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. Cell 1999; 97: 133-44.
    • (1999) Cell , vol.97 , pp. 133-144
    • McDermott, M.F.1    Aksentijevich, I.2    Galon, J.3
  • 50
    • 0030826517 scopus 로고    scopus 로고
    • Clinical spectrum of familial Hibernian fever: A 14-year follow-up study of the index case and extended family
    • 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: 806-17.
    • (1997) Mayo Clin Proc , vol.72 , pp. 806-817
    • McDermott, E.M.1    Smillie, D.M.2    Powell, R.J.3
  • 51
    • 0038479928 scopus 로고    scopus 로고
    • TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis
    • Dodé C, Cuisset L, Delpech M, Grateau G. TNFRSF1A-associated periodic syndrome (TRAPS), Muckle-Wells syndrome (MWS) and renal amyloidosis. J Nephrol 2003; 16: 435-7.
    • (2003) J Nephrol , vol.16 , pp. 435-437
    • Dodé, C.1    Cuisset, L.2    Delpech, M.3    Grateau, G.4
  • 53
    • 0034926933 scopus 로고    scopus 로고
    • The tumor-necrosis-factor receptor-associated periodic syndrome: New mutations in TNFRSF1A, ancestral origins, genotype-phenotype study and evidence for further genetic heterogeneity of periodic fevers
    • Aksentijevich I, Galon J, Soares M, et al. The tumor-necrosis-factor receptor-associated periodic syndrome: new mutations in TNFRSF1A, ancestral origins, genotype-phenotype study and evidence for further genetic heterogeneity of periodic fevers. Am J Hum Genet 2001; 69: 301-14.
    • (2001) Am J Hum Genet , vol.69 , pp. 301-314
    • Aksentijevich, I.1    Galon, J.2    Soares, M.3
  • 54
    • 0141564873 scopus 로고    scopus 로고
    • Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes
    • Aganna E, Hammond L, Hawkins PN, et al. Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes. Arthritis Rheum 2003; 48: 2632-44.
    • (2003) Arthritis Rheum , vol.48 , pp. 2632-2644
    • Aganna, E.1    Hammond, L.2    Hawkins, P.N.3
  • 55
    • 0037295409 scopus 로고    scopus 로고
    • Prospective study of anti-tumour necrosis factor receptor superfamily 1B fusion protein, and case study of anti-tumour necrosis factor receptor superfamily 1A fusion protein, in tumour necrosis factor receptor associated periodic syndrome (TRAPS): Clinical and laboratory findings in a series of seven patients
    • Drewe E, McDermott EM, Powell PT, Isaacs JD, Powell RJ. Prospective study of anti-tumour necrosis factor receptor superfamily 1B fusion protein, and case study of anti-tumour necrosis factor receptor superfamily 1A fusion protein, in tumour necrosis factor receptor associated periodic syndrome (TRAPS): clinical and laboratory findings in a series of seven patients. Rheumatology 2003; 42: 235-9.
    • (2003) Rheumatology , vol.42 , pp. 235-239
    • Drewe, E.1    McDermott, E.M.2    Powell, P.T.3    Isaacs, J.D.4    Powell, R.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.