http://www.cnr.it/ontology/cnr/individuo/prodotto/ID23968
A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations (Articolo in rivista)
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- A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Botto N.; Mariani M.; Manfredi S.; Andreassi M. G. (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- In: International Journal of Cardiology, vol. 130 (1) pp. e17 - e19. Elsevier, 2008. (literal)
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- CNR-Institute of Clinical Physiology and Fondazione Gabriele Monasterio (literal)
- Titolo
- A case report of myocardial infarction in young patient with a parental history of premature cardiovascular death: Combination of prothrombotic gene mutations (literal)
- Abstract
- We report a case ofmyocardial infarction at a young age in a subject heterozygous for the G20210A prothrombin gene variant and homozygous for the C677TMTHFR polymorphism, who presented a strong family history of atherothrombosis. Genetic screening for inherited thrombophilia, especially in the presence of a strong familiarity, may be a critical information for secondary prevention of arterial thrombosis. (literal)
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