Response to anakinra in a de novo case of neonatal-onset multisystem inflammatory disease

被引:41
作者
Hawkins, PN [1 ]
Bybee, A
Aganna, E
McDermott, MF
机构
[1] UCL Royal Free & Univ Col Med Sch, London, England
[2] St Bartholomews & Royal London Sch Med, London, England
来源
ARTHRITIS AND RHEUMATISM | 2004年 / 50卷 / 08期
关键词
D O I
10.1002/art.20357
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:2708 / 2709
页数:2
相关论文
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  • [1] De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID) -: A new member of the expanding family of pyrin-associated autoinflammatory diseases
    Aksentijevich, I
    Nowak, M
    Mallah, M
    Chae, JJ
    Watford, WT
    Hofmann, SR
    Stein, L
    Russo, R
    Goldsmith, D
    Dent, P
    Rosenberg, HF
    Austin, F
    Remmers, EF
    Balow, JE
    Rosenzweig, S
    Komarow, H
    Shoham, NG
    Wood, G
    Jones, J
    Mangra, N
    Carrero, H
    Adams, BS
    Moore, TL
    Schikler, K
    Hoffman, H
    Lovell, DJ
    Lipnick, R
    Barron, K
    O'Shea, JJ
    Kastner, DL
    Goldbach-Mansky, R
    [J]. ARTHRITIS AND RHEUMATISM, 2002, 46 (12): : 3340 - 3348
  • [2] 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, DGI
    Nicholls, A
    Granel, B
    Frances, C
    Garcier, F
    Edery, P
    Boulinguez, S
    Domergues, JP
    Delpech, M
    Grateau, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (06) : 1498 - 1506
  • [3] Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes
    Feldmann, J
    Prieur, AM
    Quartier, P
    Berquin, P
    Certain, S
    Cortis, E
    Teillac-Hamel, D
    Fischer, A
    de Saint Basile, G
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (01) : 198 - 203
  • [4] Spectrum of clinical features in Muckle-Wells syndrome and response to anakinra
    Hawkins, PN
    Lachmann, HJ
    Aganna, E
    McDermott, MF
    [J]. ARTHRITIS AND RHEUMATISM, 2004, 50 (02): : 607 - 612
  • [5] Interleukin-1-receptor antagonist in the Muckle-Wells syndrome
    Hawkins, PN
    Lachmann, HJ
    McDermott, MF
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (25) : 2583 - 2584
  • [6] Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome
    Hoffman, HM
    Mueller, JL
    Broide, DH
    Wanderer, AA
    Kolodner, RD
    [J]. NATURE GENETICS, 2001, 29 (03) : 301 - 305
  • [7] NALPs: A novel protein family involved in inflammation
    Tschopp, J
    Martinon, F
    Burns, K
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (02) : 95 - 104