References
Baglin T, Gray E, Greaves M, Hunt BJ, Keeling D, Machin S, Mackie I, Makris M, Nokes T, Perry D, Tait RC, Walker I, Watson H, British Committee for Standards in Haematology (2010) Clinical guidelines for testing for heritable thrombophilia. Br J Haematol 149:209–220
Middeldorp S, van HylckamaVlieg A (2008) Does thrombophilia testing help in the clinical management of patients? Br J Haematol 143:321–335
Vossen CY, Rosendaal FR, EPCOT Study Group (2006) Risk of arterial thrombosis in carriers of familial thrombophilia. J Thromb Haemost 4:916–918
Inbal A, Freimark D, Modan B, Chetrit A, Matetzky S, Rosenberg N, Dardik R, Baron Z, Seligsohn U (1999) Synergistic effects of prothrombotic polymorphisms and atherogenic factors on the risk of myocardial infarction in young males. Blood 93:2186–2190
Nordestgaard BG, Chapman MJ, Ray K, Borén J, Andreotti F, Watts GF, Ginsberg H, Amarenco P, Catapano A, Descamps OS, Fisher E, Kovanen PT, Kuivenhoven JA, Lesnik P, Masana L, Reiner Z, Taskinen MR, Tokgözoglu L, Tybjærg-Hansen A, European Atherosclerosis Society Consensus Panel (2010) Lipoprotein(a) as a cardiovascular risk factor: current status. Eur Heart J 31:2844–2853
Conflict of interest
None.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Cecchi, E., Marcucci, R., Ganugi, E. et al. Prothrombotic burden in a patient with recurrent thrombotic events: might an early assessment of thrombophilia be useful in the presence of a strong family history for vascular events?. Intern Emerg Med 8, 543–545 (2013). https://doi.org/10.1007/s11739-013-0928-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11739-013-0928-8