THROMBOPHILIC RISK OF INDIVIDUALS WITH COMPOUND FACTOR V LEIDEN AND PROTHROMBIN G20210A GENE MUTATION

被引：0
|
作者：
Lim, Ming Yeong [1 ]
Deal, Allison [1 ]
Conard, Jacqueline [2 ]
Dutrillaux, Fabienne [3 ]
Eid, Suhair [4 ]
Simioni, Paolo [5 ]
Moll, Stephan [1 ]
机构：
[1] Univ N Carolina, Chapel Hill, NC USA
[2] Hop Hotel Dieu, Unite Hemostase Thrombose, F-75181 Paris, France
[3] Hop Boacge, Dijon, France
[4] King Hussein Med Ctr, Aman, Jordan
[5] Univ Padua, Padua, Italy
来源：
AMERICAN JOURNAL OF HEMATOLOGY | 2014年 / 89卷 / 06期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
90
引用
收藏
页码：E43 / E43
页数：1
相关论文
共 50 条
  • [1] Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individuals
    Lim, Ming Y.
    Deal, Allison M.
    Kim, Steven
    Musty, Michael D.
    Conard, Jacqueline
    Simioni, Paolo
    Dutrillaux, Fabienne
    Eid, Suhair S.
    Middeldorp, Saskia
    Halbmayer, Walter M.
    Boneu, Bernard
    Moia, Marco
    Moll, Stephan
    [J]. EUROPEAN JOURNAL OF HAEMATOLOGY, 2016, 97 (04) : 353 - 360
  • [2] Prevalence of factor V Leiden and prothrombin G20210A gene mutation
    Al-Aama, JY
    [J]. SAUDI MEDICAL JOURNAL, 2005, 26 (11) : 1844 - 1844
  • [3] Prevalence of factor V Leiden and prothrombin G20210A gene mutation
    Irdem, A
    Devecioglu, C
    Batun, S
    Soker, M
    Sucakli, IA
    [J]. SAUDI MEDICAL JOURNAL, 2005, 26 (04) : 580 - 583
  • [4] Thrombophilic factor V (Leiden) and prothrombin (G20210A) mutation in children with Perthes' disease -: A pilot study
    Schmitz, A
    Pförtner, J
    Protzel, A
    Harbrecht, U
    [J]. ZEITSCHRIFT FUR ORTHOPADIE UND IHRE GRENZGEBIETE, 2001, 139 (02): : 143 - 146
  • [5] Thrombophilic risk of individuals with rare factor V Leiden and prothrombin 20210 compound thrombophilias.
    Moll, S
    Musty, MD
    Kim, S
    Conard, J
    Boneu, B
    Halbmayer, WM
    Scharrer, I
    Simioni, P
    [J]. BLOOD, 2003, 102 (11) : 548A - 549A
  • [6] Factor V Leiden and prothrombin gene G20210A mutation in children with cerebral thromboembolism
    Bonduel, M
    Sciuccati, G
    Hepner, M
    Pieroni, G
    Torres, AF
    Mardaraz, C
    Frontroth, JP
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2003, 73 (02) : 81 - 86
  • [7] Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation
    González-Porras, JR
    García-Sanz, R
    Alberca, I
    López, ML
    Balanzategui, A
    Gutierrez, O
    Lozano, F
    San Miguel, J
    [J]. BLOOD COAGULATION & FIBRINOLYSIS, 2006, 17 (01) : 23 - 28
  • [8] Factor V Leiden and prothrombin gene G20210A mutation in children with venous thromboembolism
    Bonduel, M
    Hepner, M
    Sciuccati, G
    Pieroni, G
    Feliú-Torres, A
    Mardaraz, C
    Frontroth, JP
    [J]. THROMBOSIS AND HAEMOSTASIS, 2002, 87 (06) : 972 - 977
  • [9] The G1691A Mutation of the Factor V Gene (Factor V Leiden) and the G20210A Mutation of the Prothrombin Gene as Risk Factors in Thrombotic Microangiopathies
    Sucker, Christoph
    Kurschat, Christine
    Hetzel, Gerd R.
    Grabensee, Bernd
    Maruhn-Debowski, Beate
    Loncar, Robert
    Ostojic, Ljerka
    Scharf, Ruediger E.
    Zotz, Rainer B.
    [J]. CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, 2009, 15 (03) : 360 - 363
  • [10] Markers of activated coagulation in patients with factor V Leiden and/or G20210A prothrombin gene mutation
    Gouin-Thibault, I
    Arkam, R
    Nassiri, S
    de la Tourette, A
    Conard, J
    Horellou, MH
    Elalamy, I
    Samama, MM
    [J]. THROMBOSIS RESEARCH, 2002, 107 (1-2) : 7 - 11
12345