Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism : Pooled analysis of 8 case-control studies including 2310 cases and 3204 controls
- Author
- EMMERICH, Joseph1 ; ROSENDAAL, Frits R2 ; CATTANEO, Marco3 ; MARGAGLIONE, Maurizio4 ; DE STEFANO, Valerio5 ; CUMMING, Tony6 ; ARRUDA, Valder7 ; HILLARP, Andreas8 ; RENY, Jean-Luc1
[1] Hôpital Européen Georges Pompidou, Service de Médecine Vasculaire (Centre Claude Bernard) et Laboratoire d'Hémostase, Paris, France
[2] Klinische Epidemiologie en Hematologie CO-P-43, Leids Universitair Medisch Centrum, Leiden, Netherlands
[3] Dipartimento di Medicina Interna, IRCCS Ospedale Maggiore, University of Milano, Milano, Italy
[4] Ospedale Casa Sollievo della Sofferenza, Unità di Ricerca in Aterosclerosi e Thrombosi, San Giovanni Rotondo, Italy
[5] Istituto di Ematologia, Università Cattolica, Roma, Italy
[6] University Department of Haematology, Haemostasis and Thrombosis Centre, Manchester Royal Infirmary, Manchester, United Kingdom
[7] Hematology-Hemotherapy Center, State University of Campinas, Campinas-SP, Brazil
[8] University of Lund, Dept. of Clinical Chemistry and Dept. for Coagulation Disorders, University Hospital, Malmö, Sweden
Study group of pooled-analysis in venous thromboembolism - Source
Thrombosis and haemostasis. 2001, Vol 86, Num 3, pp 809-816 ; ref : 44 ref
- CODEN
- THHADQ
- ISSN
- 0340-6245
- Scientific domain
- Cardiology, blood circulation, phlebology; Hematology
- Publisher
- Schattauer, Stuttgart
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Contraception Facteur V Leiden Facteur coagulation Facteur risque Femelle Gène Homme Hypercoagulabilité Mutation Prothrombine Thromboembolie Thrombophilie Thrombose Veine profonde Voie orale Appareil circulatoire pathologie Coagulopathie Génétique Hémopathie Maladie héréditaire Vaisseau sanguin pathologie Veine pathologie
- Keyword (en)
- Contraception Factor V Leiden Coagulation factor Risk factor Female Gene Human Hypercoagulability Mutation Prothrombin Thromboembolism Thrombophilia Thrombosis Deep vein Oral administration Cardiovascular disease Coagulopathy Genetics Hemopathy Genetic disease Vascular disease Venous disease
- Keyword (es)
- Anticoncepción Factor V Leiden Factor coagulación Factor riesgo Hembra Gen Hombre Hipercoagulabilidad Mutación Protrombina Tromboembolia Trombofilia Trombosis Vena profunda Vía oral Aparato circulatorio patología Coagulopatía Genética Hemopatía Enfermedad hereditaria Vaso sanguíneo patología Vena patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B12 Cardiology. Vascular system / 002B12B Blood and lymphatic vessels / 002B12B03 Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19C Platelet diseases and coagulopathies
- Discipline
- Blood diseases Cardiology. Circulatory system
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 14105829
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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