Gene polymorphisms in the thrombin activatable fibrinolysis inhibitor (TAFI) and the risk of myocardial infarction (2002)
- Authors:
- USP affiliated authors: SIMÕES, MARCUS VINÍCIUS - FMRP ; TAVELLA, MARLI HAYDEE - FMRP ; ARAUJO, AMELIA GOES DE - FMRP ; ZAGO, MARCO ANTONIO - FMRP ; MARIN NETO, JOSE ANTONIO - FMRP
- Unidade: FMRP
- Subjects: INFARTO DO MIOCÁRDIO; HEMATOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: The Hematology Journal
- ISSN: 1466-4860
- Volume/Número/Paginação/Ano: v. 3, p. 102 res. 0321, 2002
- Conference titles: Annual Meeting of the European Hematology Association
-
ABNT
FRANCO, Rendrik França et al. Gene polymorphisms in the thrombin activatable fibrinolysis inhibitor (TAFI) and the risk of myocardial infarction. The Hematology Journal. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 21 maio 2024. , 2002 -
APA
Franco, R. F., Meijers, J. C. M., Pazin-Filho, A., Simões, M. V., Marin-Neto, J. A., Tavella, M. H., et al. (2002). Gene polymorphisms in the thrombin activatable fibrinolysis inhibitor (TAFI) and the risk of myocardial infarction. The Hematology Journal. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Franco RF, Meijers JCM, Pazin-Filho A, Simões MV, Marin-Neto JA, Tavella MH, Araújo AG, Reitsma PH, Zago MA. Gene polymorphisms in the thrombin activatable fibrinolysis inhibitor (TAFI) and the risk of myocardial infarction. The Hematology Journal. 2002 ; 3 102 res. 0321.[citado 2024 maio 21 ] -
Vancouver
Franco RF, Meijers JCM, Pazin-Filho A, Simões MV, Marin-Neto JA, Tavella MH, Araújo AG, Reitsma PH, Zago MA. Gene polymorphisms in the thrombin activatable fibrinolysis inhibitor (TAFI) and the risk of myocardial infarction. The Hematology Journal. 2002 ; 3 102 res. 0321.[citado 2024 maio 21 ] - The MTHFR A1298C polymorphism and the risk of myocardial infarction
- Factor XIII Val34Leu and the risk of miocardial infarction
- Polimorfismos Val34Leu, His95Arg e G30899A do fator XIII da coagulação e risco de trombose venosa profunda
- Factor XIII gene variation and the risk of venous thrombosis
- Polimorfismos Val34Leu, HIS95ARG e G30899A do fator XIII da coagulação e risco de trombose venosa profunda
- Factor V leiden, FII G20210A and MTHFR C677T and the risk of venous trhomboembolism, arterial thrombosis and recurrent miscarriage an antiphospholipid syndrome
- The prevalence of the MTHFR C677T polymorphism in patients with preeclampsia
- A 23PB insertion in the endothelial protein C receptors (EPCR) gene and the risk of venous thrombotic disease
- HLA-H CYS282TYR mutation in patients with premature coronary atherosclerotic disease
- Gene Polymorphisms in the TNF locus and the Risk of Myocardial Infarction
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
