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家族性地中海热——附2例报道 被引量:6

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摘要 家族性地中海热(Familial Mediterranean Fever FMF)于1945年由结缔组织病专家Siegal首先报告以发热伴多发性浆膜炎为特征,有淀粉样变性倾向,最初见于地中海流域且有种旅倾向性,以后陆续报道在地区和人种分布均有扩大,我国至今未见报道,现将收治的2例报告如下:
作者 沈公印 陈超
出处 《中国罕少疾病杂志》 1999年第4期26-26,28,共2页
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  • 1韩丽芳,蔡军伟,颜亮,姚咏明.中国人群MEFV基因多态性研究[J].实用医学杂志,2006,22(11):1234-1235. 被引量:8
  • 2Ben-Chetrit E, Levy M. Familial MeditetTanean fever[ J] Lancet, 1998, 351 (9103): 659-664.
  • 3The International FMF Consortium. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever [ J ]. Cell, 1997, 90 (4) : 797-807.
  • 4French FMF Consortium. A candidate gene for familial Mediterranean fever [ J]. Nat Genet, 1997, 17 ( 1 ) : 25-31.
  • 5Bemot A, da Silva C, Petit JL, et al. Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF)[J]. Hum Mol Genet, 1998, 7 (8) : 1317-1325.
  • 6Marek-Yagel D, Berkun Y, Padeh S, et al. Clinical disease among patients heterozygous for familial Mediterranean fever [J]. Arthritis Rheum, 2009, 60 (6) : 1862-1866.
  • 7Fonnesu C, Cerquaglia C, Giovinale M, et al. Familial Mediterranean Fever: a review for clinical management [J]. Joint Bone Spine, 2009, 76 (3) : 227-233.
  • 8Ben-Chetrit E, Touitou I. Familial Mediterranean fever in the world [ J ]. Arthritis Rheum, 2009, 61 (10) :1447-1453.
  • 9Yalqinkaya F, Cakar N, Acar B, et al. The value of the levels of acute phase reactants for the prediction of familial Mediterranean fever associated amyloidosis: a case control study[J]. Rheumatol Int, 2007, 27 (6): 517-522.
  • 10Berkun Y, Padeh S, Reichman B, et al. A single testing of serum amyloid a levels as a tool for diagnosis and treatment dilemmas in familial Mediterranean fever [ J ]. Semin Arthritis Rheum, 2007, 37 (3) : 182-188.

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