MTHFR gene polymorphisms are not associated with hematologic alterations in women with recurrent pregnancy losses (2011)
- Authors:
- USP affiliated authors: SHINOHARA, ELVIRA MARIA GUERRA - FCF ; ZUGAIB, MARCELO - FM
- Unidades: FCF; FM
- Subjects: POLIMORFISMO; ABORTO ESPONTÂNEO
- Language: Inglês
- Imprenta:
- Publisher: European Hematology Association (EHA)
- Publisher place: Hague
- Date published: 2011
- Source:
- Título do periódico: Abstracts
- Conference titles: Annual Congress of the European Hematology Association (EHA)
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ABNT
GUERRA-SHINOHARA, Elvira Maria et al. MTHFR gene polymorphisms are not associated with hematologic alterations in women with recurrent pregnancy losses. 2011, Anais.. Hague: European Hematology Association (EHA), 2011. . Acesso em: 19 abr. 2024. -
APA
Guerra-Shinohara, E. M., Giusti, K. C. da S., Lázaro, R. J., Monteiro, N., Bertinato, F., Seino, F. M., et al. (2011). MTHFR gene polymorphisms are not associated with hematologic alterations in women with recurrent pregnancy losses. In Abstracts. Hague: European Hematology Association (EHA). -
NLM
Guerra-Shinohara EM, Giusti KC da S, Lázaro RJ, Monteiro N, Bertinato F, Seino FM, Britto J, Cavalcante S, Carvalho M, Amorim Filho A, Zugaib M. MTHFR gene polymorphisms are not associated with hematologic alterations in women with recurrent pregnancy losses. Abstracts. 2011 ;[citado 2024 abr. 19 ] -
Vancouver
Guerra-Shinohara EM, Giusti KC da S, Lázaro RJ, Monteiro N, Bertinato F, Seino FM, Britto J, Cavalcante S, Carvalho M, Amorim Filho A, Zugaib M. MTHFR gene polymorphisms are not associated with hematologic alterations in women with recurrent pregnancy losses. Abstracts. 2011 ;[citado 2024 abr. 19 ] - Efeito de polimorfismos genéticos relacionados ao metabolismo de folato e da homocisteína na etiologia dos abortos espontâneos recorrentes
- Polymorphisms in fibrinogen (C.148C>T and C.455G>A) gene and thrombomodulin (C.1418C>T) gene and their role in the occurrence of recurrent miscarriages
- Effect of polymorphisms in key enzymes of homocysteine metabolism and their association with recurrent pregnancy loss
- Variant of TC2 c. 776C>g polymorphism is associated with elevated risk of recurrent pregnancy loss
- Association between polymorphisms in the transcobalamin II gene (TC2 C. 776C> G and C. TC267C>G) and methylenetetrahydrofolate reductase gene (MTHFR 677C>T) and risk of having recurrent miscarriages
- Frequencies of autoantibodies in women with recurrent pregnancy losses
- The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss
- Polymorphisms in thrombin-activatable fibrinolysis inhibitor and plasminogen activator inhibitor type 1 in women with primary recurrent pregnancy loss
- Association between the polymorphisms MTHFR c. 677C>T and MTHFR c. 1298A>C and haplotypes with recurrent miscarriages
- Frequency of autoantibodies in women with recurrent miscarriage history
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