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先天性纤维蛋白原缺乏症行子宫切除术 被引量:2

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出处 《生殖医学杂志》 CAS 2008年第4期307-309,共3页 Journal of Reproductive Medicine
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参考文献14

  • 1al-Mondhiry H, Ehmann WC. Congenital afibrinogenemia [J]. Am J Hematol, 1994,46 (4):343-347.
  • 2李春怀,梁东,陈银波,雷梅芳.遗传性纤维蛋白原缺乏症1例[J].中国实验诊断学,2005,9(1):142-143. 被引量:2
  • 3戴碧涛,王莉佳,王世一.先天性纤维蛋白原缺乏症家族发病三例[J].中华儿科杂志,2002,40(12):763-763. 被引量:6
  • 4Santacrocea R, Cappucci F, Pisanellia D, et al. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group[J]. Blood Coagul Fibrinolysis, 2006, 17 (4) 235-240.
  • 5Asselta R, Duga S, Tenchini ML. The molecular basis of quantitative fibrinogen disorders[J].J Thromb Haemost, 2006,4(4) :2115-2119.
  • 6Neerman-Arbez M. Fibrinogen gene mutations accounting for congenital afibrinogenemia [J]. Ann N Y Acad Sci, 2001, 936(6) :496-508.
  • 7Vu D, Bolton-Maggs PH, Parr JR, et al. Congenital afibrinogenemia:identification and expression of a missense mutation in FGB impairing fibrinogen secretion[J].Blood, 2003,102 (13):4413-4415.
  • 8Neerman-Arbez M, Vu D, Abu-Libdeh B, et al. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family[J]. Blood, 2003,101(9):3492-3494.
  • 9Neerman-Arbez M, de Moerloose P, Bridel C, et al. Mutations in the fibrinogen alpha gene account for the majority of cases of congenital afibrinogenemia [J]. Blood, 2000,96(1) : 149-152.
  • 10Evron S, Anteby SO, Brzezinsky A, et al. Congenital afibrinogenemia and recurrent early abortion: a case report[J]. Eur J Obstet Gynecol Reprod Biol, 1985,19(5) :307-311.

二级参考文献4

  • 1Brennan SO, Fellows AP, GeogePM. Identification and characterization of five new fibrinogen gene polymorphisms[J]. Ann NY Acad Sci, 2001,936:536.
  • 2Neerman-Arbez M, de Moerloosep, Honsberger A, et al. Mutation in the fibrinogen A alpha geneaccount for the majority of cases of congenital afibrinogenemia[J]. Blood, 2000,96(1):149.
  • 3Asselta R, DugaS, simonic T, et al. Congenital afibrinnogenemia:mutation leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNA[J]. Blood,2000,96(7) :2496.
  • 4Asselta R, SpenaS, Dugas, et al. Analysis of Iranian patients allow the identification of the first truncating mutation in the fibrinogen B beta-chain gene causing afibrinogenemia[J]. Haematologica, 2002,87(8) :855.

共引文献5

同被引文献32

  • 1李春怀,梁东,陈银波,雷梅芳.遗传性纤维蛋白原缺乏症1例[J].中国实验诊断学,2005,9(1):142-143. 被引量:2
  • 2方怡,王学锋,傅启华,武文漫,丁秋兰,戴菁,周荣富,王文斌,谢爽,王鸿利.一个纤维蛋白原γ链Arg275His突变导致的遗传性异常纤维蛋白原血症家系[J].中华医学遗传学杂志,2005,22(2):201-203. 被引量:27
  • 3Fellowes AD, Brennan SO, George PM. Identification and characterization of five new fibrinogen gene polymorphisms[J]. Ann N Y Acad Sci, 2001, 936: 536-541.
  • 4Asselta R, Spena S , Duga S, et al. Molecular genetics of quantitative fibrinogen disorders [J]. Cardiovasc Hematol Agents Med Chem, 2007, 5 (2) : 163-173.
  • 5Neerman-Arbez M, de Moerloose P, Bridel C, et al. Mutations in the fibrinogen A alpha gene accout for the majority of cases of congenital a fibrinogenemia[J]. Blood, 2000, 96 (1) : 149-152.
  • 6Asselta R, Duga S, Tenchini ML, et al. The molecular basis of quantitative fibrinogen disorders[J]. J Thromb Haemost, 2006, 4 (10) : 2115-2129.
  • 7Hill M, Dolan G. Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias [J]. Haemophilia, 2008, 14 (5) : 889-897.
  • 8MATSUDA M, SUGO T. HEREDITARY disorders of fibrino- gen [ J ]. Ann N Y Acad Sci, 2001,936 : 65- 88.
  • 9纤维蛋白原基因突变库网址http ://site. geht. org/site/Pratiques- Professionnelles/Base- de- donnees- Fibrinogene! Database- English- Version/Fibrinogen- variants- Database- _ 79. html.
  • 10NEERMAN-ARBEZ M, DE MOERLOOSE P, BRIDEL C, et al. Mutations in the brinogen Aa gene account for the majori- ty of cases of congenital a fibrinogenemia [ J ]. Blood,2000, 96(1) :149-152.

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