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不完全型川崎病合并嗜血细胞综合征1例 被引量:3

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摘要 1病例资料
作者 郑嵘君
出处 《中国现代药物应用》 2014年第7期182-183,共2页 Chinese Journal of Modern Drug Application
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参考文献6

  • 1Ayusawa M, Sonobe T, Uemura S, et al. Revision of diagnostic guidelines for Kawasaki disease(the 5th revised edition). Pediatr Int, 2005, 47(2):232-234.
  • 2Newburger JW, Takahashi M, Gerber MA, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Pediatrics, 2004,110( 17):2747-2771.
  • 3汤永民.加强儿童噬血细胞综合征的早期诊断与干预研究[J].临床儿科杂志,2009,27(8):705-708. 被引量:10
  • 4Henter JI, Home A, Aric 6 M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer, 2007,48(2): 124-131.
  • 5Freeman HR, Ramanan AV. Review of haemophagocytic lymphohistiocytosis.Arch Dis Child, 2011,96(7):688-693.
  • 6Giordani L, Quaranta MG, Marchesi A, et al. ncreased frequency of immunoglobulin (Ig)A-secreting cells following Toll-like receptor (TLR)-9 engagement in patients with Kawasaki disease. Clin Exp Immunol, 2011,163(3):346-353.

二级参考文献18

  • 1汤永民,廖婵.噬血细胞综合征的分子生物学基础及其发病机制[J].实用儿科临床杂志,2006,21(9):513-516. 被引量:11
  • 2Farquhar JW, Claireaux AE. Familial haemophagocytic reticulosis [J]. Arch Dis Child, 1952,27(136) :519-525.
  • 3Menasche G, Feldmann J, Fischer A, et al. Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis [J]. Immunol Rev, 2005,203 : 165-179.
  • 4Toitt I, Brostoff J, Male D. Immnulogy [M]. 6th ed. Harcourt Publishers Limited, 2001 : 235-258.
  • 5Stepp SE, Dufourcq-Lagelouse R, Le Deist F, et al. Perforin gene defects in familial hemophogocytic lympho- histiocytosis [J]. Science, 1999,286(5446) : 1957-1959.
  • 6Katano H, Cohen JI. Pefforin and lymphohistiocytic proliferative disorders [ J ]: Br J Haematol, 2005,128 (6) : 739- 750.
  • 7Zur Stadt U, Beutel K, Kolberg S, et al. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STXII, and RAB27A [J]. Hum Mutat, 2006,27(1) :62-68.
  • 8Feldmann J, Callebaut I, Raposo G, et al. Muncl3-4 is essential for eytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistioeytosis (FHL3) [J]. Cell,2003,115(4) :461-473.
  • 9Yamamoto K, Ishii E, Sako M, et al. Identification of novel MUNC13-4 mutations in familial haemophagocytic lym-phohistiocytosis and functional analysis of MUNC13- 4-deficient cytotoxic T lymphocytes[J].J Med Genet, 2004,41 (10) :763-767.
  • 10zur Stadt U, Schmidt S, Kasper B, et al. Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11[J]. Hum Mol Genet,2005,14(6) :827-834.

共引文献9

同被引文献26

  • 1刘志刚,王亚超.小儿川崎病并嗜血细胞综合征1例[J].西安交通大学学报(医学版),2005,26(1):51-51. 被引量:2
  • 2施虹,程佩萱,王宏伟.巨噬细胞活化综合征[J].实用儿科临床杂志,2006,21(3):179-182. 被引量:4
  • 3Dogra S, Gehlot A, Suri D, et al. Incomplete Kawasaki Disease fol-lowed by Systemic Onset Juvenile Idiopathic Arthritis- The Diag- nostic Dilemma[J]. Indian J Pediatr,2013,80(9):783-785.
  • 4Reed A, Haugen M, Pachman L M. Abnormalities in serum osteo- calcin values in children with chronic rheumatic diseases[J]. Jour- nal of Pediatrics,1990,116(4) : 574-580.
  • 5Ayusawa M, Sonobe T, Uemura S, et aL Revision of diagnostic guidelines for Kawasaki disease(the 5th revised edition)[J].Pediatr Int,2005,47(2):232-234.
  • 6Binstadt B A, Levine J C, Nigrovic P A, et al. Coronary artery dila- tion among patients presenting with systemic-onset juvenile idio- pathic arthritis[J].Pediatrics,2005,116:e89-e93.
  • 7Dong S, Bout-Tabaku S, Texter K, et al. Diagnosis of Systemic-On- set Juvenile Idiopathic Arthritis after Treatment for Presumed Kawasaki Disease[J]. The Journal of pediateics Volume, 2015, 166 (5):1283-1288.
  • 8Wang W, Gong F, Zhu W, et al. Macrophage activation syndrome in Kawasaki Disease: more common than we thought?[J]. Semin Arthritis Rheum, 2015,44(4):405-410.
  • 9Minoia F, Davi S, Home A, et al. Clinical features, treatment, and outcome of macrophage activation syndrome complicating sys- temic juvenile idiopathic arthritis: a multinational, multicenter study of 362 patients[J]. Arthritis Rheumatol,2014,66(11):3160- 3169.
  • 10Vastert S J, Kuis W, Grom A A. Systemic JIA:new developments in the understanding of the pathophysiology and therapy[J].Best Pract Res Clin Rheumatol,2009,23(5):655-664.

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