Literature DB >> 25074526

Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.

Suar Çakı Kılıç1, F Dilara İçağasıoğlu2, A Sami Güven2, Ergül Berber3.   

Abstract

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Year:  2014        PMID： 25074526      PMCID： PMC4111834          DOI： 10.2450/2014.0022-14

Source DB:  PubMed          Journal:  Blood Transfus        ISSN： 1723-2007            Impact factor:   3.443


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  5 in total

1.  Characterization of the genetic basis of FXI deficiency in two Turkish patients.

Authors:  E Berber; V Rimoldi; S Usluer; S Aksu; Y Pekcelen; S H Cağlayan; S Duga
Journal:  Haemophilia       Date:  2009-12-14       Impact factor: 4.287

2.  Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity.

Authors:  F Peyvandi; D Di Michele; P H B Bolton-Maggs; C A Lee; A Tripodi; A Srivastava
Journal:  J Thromb Haemost       Date:  2012-09       Impact factor: 5.824

3.  One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews.

Authors:  O Shpilberg; H Peretz; A Zivelin; R Yatuv; A Chetrit; T Kulka; C Stern; E Weiss; U Seligsohn
Journal:  Blood       Date:  1995-01-15       Impact factor: 22.113

4.  Molecular characterization of FXI deficiency.

Authors:  Ergul Berber
Journal:  Clin Appl Thromb Hemost       Date:  2010-03-22       Impact factor: 2.389

Review 5.  Occurrence of thrombosis in rare bleeding disorders.

Authors:  Arlette Ruiz-Saez
Journal:  Semin Thromb Hemost       Date:  2013-08-08       Impact factor: 4.180
  5 in total

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