Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individuals-Reference-Cited by-同舟云学术

Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individuals

Published:2016-02-18 Issue:4 Volume:97 Page:353-360
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Lim Ming Y.¹,Deal Allison M.²,Kim Steven³,Musty Michael D.⁴,Conard Jacqueline⁵,Simioni Paolo⁶,Dutrillaux Fabienne⁷,Eid Suhair S.⁸,Middeldorp Saskia⁹,Halbmayer Walter M.¹⁰,Boneu Bernard¹¹,Moia Marco¹²,Moll Stephan¹

Affiliation:

1. Division of Hematology/Oncology; Department of Medicine; University of North Carolina; Chapel Hill NC USA

2. Lineberger Comprehensive Cancer Center Biostatistics Core; Chapel Hill NC USA

3. Hematology/Oncology; St. Jude Heritage Medical Group; Fullerton CA USA

4. Center for Applied Genomics & Precision Medicine; Duke University Medical Center; Durham NC USA

5. Haemostasis-Thrombosis Unit; Hotel-Dieu University Hospital; Paris France

6. Department of Medicine - DIMED; University of Padua Medical School; Padua Italy

7. Haemostasis Unit; University Hospital of Dijon; Dijon France

8. Princess Iman Research and Laboratory Sciences Center; King Hussein Medical Center; Amman Jordan

9. Academic Medical Center; Department of Vascular Medicine; Amsterdam The Netherlands

10. Institute of Laboratory Medicine; Municipal Hospital Hietzing-Rosenhuegel; Vienna Austria

11. Haemostasis Laboratory; Rangueil Hospital; Toulouse France

12. Angelo Bianchi Bonomi Hemophilia and Thrombosis Centre; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Milan Italy

Funder

American Society of Hematology

Centers for Disease Control and Prevention

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12738/fullpdf

Reference31 articles.

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2. A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis;Poort;Blood,1996

3. Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls;Simone;Eur J Epidemiol,2013

4. Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis;Mainardi;Blood,1999

5. Combined genetic defect (homogeneity for factor V Leiden and heterogeneity for prothrombin G20210A allele), in a young patient, with recurrent deep vein thrombosis and serious postphlebitic syndrome - a case report;Mitsis;Angiology,2000

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