Factor V leiden, FII G20210A and MTHFR C677T and the risk of venous trhomboembolism, arterial thrombosis and recurrent miscarriage an antiphospholipid syndrome (2002)
- Authors:
- USP affiliated authors: ZAGO, MARCO ANTONIO - FMRP ; ARAUJO, AMELIA GOES DE - FMRP ; TAVELLA, MARLI HAYDEE - FMRP ; LOUZADA JÚNIOR, PAULO - FMRP
- Unidade: FMRP
- Subjects: FARMACOLOGIA; DOENÇAS VASCULARES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: The Hematology Journal
- ISSN: 1466-4860
- Volume/Número/Paginação/Ano: v. 3, p. 109 res. 0346, 2002
- Conference titles: Annual Meeting of the European Hematology Association
-
ABNT
PIERONI, Fabiano et al. Factor V leiden, FII G20210A and MTHFR C677T and the risk of venous trhomboembolism, arterial thrombosis and recurrent miscarriage an antiphospholipid syndrome. The Hematology Journal. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 13 maio 2024. , 2002 -
APA
Pieroni, F., Freitas, M. V. C., Zago, M. A., Araújo, A. G., Tavella, M. H., Louzada Júnior, P., & Franco, R. F. (2002). Factor V leiden, FII G20210A and MTHFR C677T and the risk of venous trhomboembolism, arterial thrombosis and recurrent miscarriage an antiphospholipid syndrome. The Hematology Journal. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Pieroni F, Freitas MVC, Zago MA, Araújo AG, Tavella MH, Louzada Júnior P, Franco RF. Factor V leiden, FII G20210A and MTHFR C677T and the risk of venous trhomboembolism, arterial thrombosis and recurrent miscarriage an antiphospholipid syndrome. The Hematology Journal. 2002 ; 3 109 res. 0346.[citado 2024 maio 13 ] -
Vancouver
Pieroni F, Freitas MVC, Zago MA, Araújo AG, Tavella MH, Louzada Júnior P, Franco RF. Factor V leiden, FII G20210A and MTHFR C677T and the risk of venous trhomboembolism, arterial thrombosis and recurrent miscarriage an antiphospholipid syndrome. The Hematology Journal. 2002 ; 3 109 res. 0346.[citado 2024 maio 13 ] - Polimorfismos Val34Leu, His95Arg e G30899A do fator XIII da coagulação e risco de trombose venosa profunda
- 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
- Factor V leiden, FH G20210A and mither C677T and the risk of venous thromboembolism, arterial thrombosis and recurrent miscarriage in APS
- New interactive effects involving factor XIII gene polymorphisms in venous thrombotic disease
- Rearrangements of the 'beta'-globin gene cluster in apparently typical ''beta' POT.s' haplotypes
- Absence of the E2 allele of apolipoprotein in Amerindians
- 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
- Factor XIII (FXIII Val34Leu, His95Arg and G30899A polymorphisms and the risk of deep venous thrombosis
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