Literature DB >> 9493607

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.

P Bucciarelli, F Franchi, A Alatri, P Bettini, M Moia.   

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Year:  1998        PMID： 9493607

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  3 in total

1.  Prothrombin 20210G/A mutation in two patients with mesenteric ischemia.

Authors:  A Balian; A Veyradier; S Naveau; M Wolf; S Montembault; V Giraud; E Borotto; C Henry; D Meyer; J C Chaput
Journal:  Dig Dis Sci       Date:  1999-09       Impact factor: 3.199

2.  Concomitant homozygosity for the prothrombin gene variant with mild deficiency of antithrombin III in a patient with multiple hepatic infarctions: a case report.

Authors:  Theodore Emmanuelle; Belkys Husein; Javaid Iqbal; M Macheta; Peter Isaacs
Journal:  J Med Case Rep       Date:  2010-04-29

3.  Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.

Authors:  Peijin Zhang; Jing Zhang; Guixiang Sun; Xiuyin Gao; Hui Wang; Wenjun Yan; Hao Xu; Maoheng Zu; He Ma; Wei Wang; Zhaojun Lu
Journal:  PLoS One       Date:  2014-04-22       Impact factor: 3.240
  3 in total

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