| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1015742158 |
| P356 | DOI | 10.1186/1479-5876-10-235 |
| P932 | PMC publication ID | 3543285 |
| P698 | PubMed publication ID | 23171482 |
| P5875 | ResearchGate publication ID | 233744859 |
| P2093 | author name string | Angelo B Cefalù | |
| Davide Noto | |||
| Maurizio R Averna | |||
| Pierpaolo Di Micco | |||
| Giuseppe Castaldo | |||
| Federica Zarrilli | |||
| Rossella Tomaiuolo | |||
| Antonietta Caruso | |||
| Chiara Bellia | |||
| Marcello Ciaccio | |||
| Rosanna Di Fiore | |||
| Sandro Quaranta | |||
| P2860 | cites work | Acute myocardial infarction in the young--The University of Michigan experience | Q28192009 |
| Activity of mannose-binding lectin in centenarians | Q28257298 | ||
| Myocardial infarction in young patients | Q33735292 | ||
| Universal definition of myocardial infarction | Q34007701 | ||
| Risk assessment for recurrent venous thrombosis | Q34153343 | ||
| Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction: a systematic review | Q34465539 | ||
| Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66,155 cases and 91,307 controls. | Q34497859 | ||
| MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis. | Q34974721 | ||
| Genetic associations in large versus small studies: an empirical assessment | Q35070873 | ||
| Different outcome of six homozygotes for prothrombin A20210A gene variant | Q36789863 | ||
| Molecular genetics of myocardial infarction | Q36843011 | ||
| Genetic basis of thrombosis | Q37804873 | ||
| No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age. | Q44342380 | ||
| Long-term prognosis of patients having acute myocardial infarction when | Q45100444 | ||
| The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease | Q46672617 | ||
| Fetuin-A serum levels are not correlated to kidney function in long-lived subjects. | Q54318806 | ||
| Common Genetic Variation in Five Thrombosis Genes and Relations to Plasma Hemostatic Protein Level and Cardiovascular Disease Risk | Q57740432 | ||
| Genetic susceptibility to death from coronary heart disease in a study of twins | Q72290929 | ||
| Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease | Q73303010 | ||
| Thermolabile methylenetetrahydrofolate reductase, homocysteine, and cardiovascular disease risk: the European Concerted Action Project | Q78710488 | ||
| A mannose-binding lectin-defective haplotype is a risk factor for gastric cancer | Q80009233 | ||
| P921 | main subject | acute myocardial infarction | Q18558122 |
| P304 | page(s) | 235 | |
| P577 | publication date | 2012-11-21 | |
| P1433 | published in | Journal of Translational Medicine | Q15716664 |
| P1476 | title | Prothrombotic gene variants as risk factors of acute myocardial infarction in young women | |
| P478 | volume | 10 |
| Q36606238 | ADRB2 polymorphisms predict the risk of myocardial infarction and coronary artery disease |
| Q35997177 | Acute coronary syndromes in young women - the scale of the problem and the associated risks |
| Q50903704 | Genetic risk factors for myocardial infarction more clearly manifest for early age of first onset. |
| Q45841684 | Prevalence of genetic prothrombotic risk factors: 1691G > A FV, 20210G > A PT and 677C > T MTHFR mutations in the Bosnian population. |
| Q40838962 | Prevalence of thrombophilic disorders in takotsubo patients: the (ThROmbophylia in TAkotsubo cardiomyopathy) TROTA study |
| Q42670330 | Prothrombin G20210A (rs1799963) polymorphism increases myocardial infarction risk in an age-related manner: A systematic review and meta-analysis |
Search more.